Botulinum toxin

Botulinum toxin A

Clinical data
Legal status	US: ℞-only
Routes of administration	IM (approved), SC, intradermal, into glands
Identifiers
CAS Number	93384-43-1 N
ATC code	M03AX01
DrugBank	DB00083 N
ChemSpider	none
Chemical data
Formula	C6760H10447N1743O2010S32
Molar mass	150 kDa (150,000 g/mol)
NY (what is this?)  (verify)

Bontoxilysin
Identifiers
EC number	3.4.24.69
Databases
IntEnz	IntEnz view
BRENDA	BRENDA entry
ExPASy	NiceZyme view
KEGG	KEGG entry
MetaCyc	metabolic pathway
PRIAM	profile
PDB structures	RCSB PDB PDBe PDBsum
Gene Ontology	AmiGO / EGO
Search PMC articles PubMed articles NCBI proteins

Botulinum toxin (BTX) is a neurotoxic protein produced by the bacterium Clostridium botulinum and related species.^[1] It is also produced commercially for medical, cosmetic, and research use. There are two main commercial types: botulinum toxin type A and botulinum toxin type B.^[2]

Infection with the bacterium may result in a potentially fatal disease called botulism. Botulinum is the most acutely lethal toxin known, with an estimated human median lethal dose (LD₅₀) of 1.3–2.1 ng/kg intravenously or intramuscularly and 10–13 ng/kg when inhaled.^[3]

Botulinum toxin types A and B are used in medicine for, among others, upper motor neuron syndrome, focal hyperhidrosis, blepharospasm, strabismus, chronic migraine and bruxism. It is also widely used in cosmetic treatments. The U.S. Food and Drug Administration requires a boxed warning stating that when locally administered the toxin may spread from the injection site to other areas of the body, causing botulism. The warning was the result of deaths associated with its uses.^[4][5] The commercial form is marketed under the brand name Botox, among others. Botox is made by Allergan.^[6]

Uses

Medical uses

Botulinum toxin is used for a number of medical problems.^[7] When injected in small amounts, it can effectively weaken a muscle for a period of three to four months.^[8]

It is used in the treatment of spasms and dystonias.^[9]

The conditions approved for treatment with botulinum toxin include:^{[4][5][10][11]}

• cervical dystonia (spasmodic torticollis), a neuromuscular disorder of the head and neck, which makes someone involuntarily jolt their head to one side;^[12][13]
• blepharospasm, uncontrolled muscle contraction or twitch of the eyelid;^[14]
• severe primary axillary hyperhidrosis, a condition of excessive sweating;^[15][16]
• chronic migraine, defined by patient history and high frequency of occurrence;^[11][17][18]
• strabismus, improper alignment of the eyes (heterotropia; colloquially "crossed eyes").^[19]

Other adult uses of botulinum toxin type A include:

• oesophageal achalasia, failure of smooth muscle relaxation, such that the oesophageal sphincter fails to open when needed;^[20]
• bruxism, parafunctional teeth grinding/jaw clenching, by injection into masticating muscles (e.g., the masseter);^[21]
• chronic focal neuropathies: It has been reported that local intradermal injection of BTX-A may be helpful, as the analgesic effects are independent of changes in muscle tone;^[22]
• idiopathic and neurogenic detrusor overactivity;^[23]
• vaginismus to reduce spasm of the vaginal muscles;^[24]
• movement disorders associated with injury or disease of the central nervous system, including trauma, stroke, multiple sclerosis, Parkinson's disease, or cerebral palsy;
• focal dystonias affecting the limbs, face, jaw, or vocal cords;^[16]
• obesity, i.e., as an aid in weight loss, by increasing the gastric emptying time;^[25]
• detrusor sphincter dyssynergia and benign prostatic hyperplasia;^[23]
• vocal cord dysfunction, including spasmodic dysphonia and tremor;^[16]
• painful bladder syndrome;^[23]
• anal fissure;^[26]
• gastric cancer;^[27]
• allergic rhinitis.^[16]

Uses of botulinum toxin type A in children include:

• muscle spasms in cerebral palsy;^[4][5][10]
• incontinence,^[28] including incontinence due to overactive bladder^[29] and incontinence due to neurogenic bladder.^[30]

Emerging uses for botulinum toxin type A include chronic musculoskeletal pain.^[31]

Cosmetic

In cosmetic applications, injection of botulinum toxin can be used to prevent development of wrinkles by paralyzing facial muscles.^[32] Following treatment, results are usually seen within 3–5 days, however it can take up to 2 weeks to see full results.

Adverse effects

Off-target effects

Off-target, or side effects, that have been reported are consistent with the mechanism of the protein toxin's function, and its known modes of action; there are, consequently, two major areas of off-target effects: allergic reaction, and paralysis of the wrong muscle group.

Adverse events or reactions from cosmetic use include facial paralysis resulting in inappropriate facial expression, drooping eyelid, and double vision, bruising, swelling, or redness at the site of injection, headaches, dysphagia, flu-like syndromes, blurred vision, dry mouth, fatigue, and allergic reactions.^[33] Cosmetic treatments are of limited duration; they can be as short as six weeks, but can last from two to three months; hence paralysis side-effects can have the same durations. The results of inappropriate facial expression, drooping eyelid, and double vision are foremost,^[32] but the list extends to uneven smiling, and loss of the ability to close ones eyes; at least in some cases, these effects are reported to dissipate in the weeks after treatment. Bruising at the site of injection is not a side effect of the toxin but rather of the mode of administration, and is reported as preventable if the clinician applies pressure to the injection site; when it occurs, it is reported in specific cases to last 7–11 days. When injecting the masseter muscle of the jaw, loss of muscle function can result in a loss or reduction of power to chew solid foods.^[33]

Individuals who are pregnant, have egg allergies, or a neuromuscular disorder are advised to avoid botulinum toxin drugs, and breastfeeding mothers are advised to consult their doctors.^[32]

The psychological and emotional consequences associated with cosmetic treatments is not yet well documented, and reports are not yet consistent. A study of treatment of glabellar lines with consequent reduction of ability to frown correlated with a "more positive mood[s]",^[34] while a study on the treatment of "crow's feet" or "laughter lines" suggested the opposite effect as a consequence of the impact of the treatment on the patient's ability to smile.^[35]

Poisoning

If the symptoms of botulism are diagnosed early, an equine antitoxin, use of enemas, and extracorporeal removal of the gut contents can be used to treat the food-borne illness. Wound infections can be treated surgically. Information regarding methods of safe canning, and public education about the disease are methods of prevention. Tests to detect botulism include a brain scan, a nerve conduction test, and a tensilon test for myasthenia gravis to differentiate botulism from other diseases that manifest in the same way. Electromyography can be used to differentiate myasthenia gravis and Guillain-Barré syndrome, diseases that botulism often mimics. Toxicity testing of serum specimens, wound tissue cultures, and toxicity testing, and stool specimen cultures are the best methods for identifying botulism. Laboratory tests of the patient's serum or stool, which are then injected into mice, are also indicative of botulism.^[36] The faster way to detect botulinum toxin in people, however, is using the mass spectrometer technology, because it reduces testing time to three or four hours and at the same time can identify the type of toxin present.^[37]

The case fatality rate for botulinum poisoning between 1950 and 1996 was 15.5%, down from about 60% over the previous 50 years.^[38] Death is generally secondary to respiratory failure due to paralysis of the respiratory muscles, so treatment consists of antitoxin administration and artificial ventilation until the neurotoxins are excreted or metabolised. If initiated on time, these treatments are quite effective, although antisera can not affect toxin polypeptides that have already entered cells.^[39] Occasionally, functional recovery may take several weeks to months or more.

Two primary botulinum antitoxins are available for treatment of botulism.

• Trivalent (A,B,E) botulinum antitoxin is derived from equine sources using whole antibodies (Fab and Fc portions). This antitoxin is available from the local health department via the CDC in the USA.
• The second antitoxin is Heptavalent (A,B,C,D,E,F,G) botulinum antitoxin, which is derived from "despeciated" equine IgG antibodies, which have had the Fc portion cleaved off, leaving the F(ab')2 portions. This less immunogenic antitoxin is effective against all known strains of botulism where not contraindicated, and is available from the United States Army. On June 1, 2006, the US Department of Health and Human Services awarded a $363 million contract with Cangene Corporation for 200,000 doses of heptavalent botulinum antitoxin over five years for delivery into the Strategic National Stockpile beginning in 2007.^[40]

Links to deaths

The US Food and Drug Administration (FDA) has formally linked complications from use of botulinum drug products to patient deaths. In September 2005, the Journal of American Academy of Dermatology communicated information from the FDA reporting 28 deaths between 1989 and 2003 associated with the use of botulinum toxin products, though none attributed to cosmetic use.^[33]

In January 2008, a petition filed by Public Citizen with the FDA requested regulatory action concerning the possible spread of the effects of botulinum toxin injectable products, including Botox and Myobloc, from the site of injection to other parts of the body.^[41]

On February 8, 2008, the FDA announced its conclusion that this class of drugs had "been linked in some cases to adverse reactions, including respiratory failure and death, following treatment of a variety of conditions using a wide range of doses", due to its ability to spread to areas distant from the site of the injection.^[4] The communication was a result of ongoing FDA safety reviews of the on-market product, and found adverse reactions associated with uses that were both FDA-approved and non-approved, the most severe being in children with cerebral palsy treated for limb spasticity (not approved for either adult or pediatric use).^[4]

On April 30, 2009, based on a continuing safety evaluation of on-market botulinum toxin products, the FDA reported its conclusion that the prescribing information for Botox, Botox Cosmetic, and Myobloc must be updated to ensure their continued safe use. On July 31, 2009, FDA, under the authorities granted by the Food and Drug Administration Amendments Act of 2007, approved revisions to the prescribing information (see following).

Further, on April 30, the FDA announced an update to its mandatory boxed warnings for four on-market products—Botox, Botox Cosmetic, Myobloc, and Dysport—and on July 31, it approved revisions to the prescribing information for the four drugs. In the revisions, it made clear that the effects of botulinum toxin may spread from the area of injection to other body areas, causing symptoms similar to those of botulism, including potentially life-threatening swallowing and breathing difficulties resulting in patient death.^[5] Most accumulated adverse reactions were again reported for pediatric palsy patients (off-label use, see above), though adverse reaction reports were also fielded for adult patients involved in both approved and unapproved uses; the FDA emphasized that at recommended/approved doses there were few serious adverse reactions for common, standard treatments for focal hyperhidrosis, blepharospasm, or strabismus, or for cosmetic/dermatologic treatments, e.g., for glabellar lines (i.e., when label instructions were followed).^[5] The FDA further emphasized that the activity units of each product do not interconvert, specifically that "different botulinum toxin products are not interchangeable, because the units used to measure the products are different",^[5] and required a change in the established drug names of older drugs, from:

• Botox and Botox Cosmetic to onabotulinumtoxinA,
• Dysport to abobotulinumtoxinA (already in place, so no change), and from
• Myobloc to rimabotulinumtoxinB,

doing so to "emphasize the differing dose to potency ratios of [each of] these products."^[5][10]

A further FDA communication aimed at health care professionals reiterated the approved drugs for each adult indication:

• cervical dystonia: OnabotulinumtoxinA (Botox), AbobotulinumtoxinA (Dysport), and RimabotulinumtoxinB (Myobloc);
• blepharospasm, severe primary axillary hyperhidrosis, strabismus: OnabotulinumtoxinA (Botox); and
• temporary cosmetic treatment of glabellar lines: OnabotulinumtoxinA (Botox), AbobotulinumtoxinA (Dysport).

These have been extended, through later announcement, to include:

• adult headache prevention in cases of chronic migraine: OnabotulinumtoxinA (Botox),

which is defined for patients having a history of migraine, and experiencing a headache on most days of the month."^[11]

In the 2009 communication to professionals, the FDA reiterated the foregoing adverse reaction observations and the possibility of "unexpected loss of strength or muscle weakness", leading to:

• double vision, blurred vision or drooping eyelids;
• dysphonia (hoarseness, trouble talking), dysarthria (trouble enunciating words), or trouble swallowing;
• trouble breathing; or
• loss of bladder control

and that "swallowing and breathing difficulties can be life-threatening" (i.e., that there have been "deaths related to the effects of spread of botulinum toxin").^[10] The communication to professionals reiterated that pediatric spasticity patients were at greatest risk from existing treatment practices, but also that approved and lower doses used to treat cervical dystonia and adult spasticity were also seen among the "cases of toxin spread", so that in all cases of drug administration, patients and their caregivers needed to:

"Pay close attention for any signs or symptoms of adverse events. [and] Seek immediate medical attention… [in the case of] difficulty swallowing or talking, trouble breathing, or muscle weakness…"

and that these events may occur "as late as several weeks after treatment."^[10]

Warning labels

In January 2009, the Canadian government warned that botulinum toxin products can have the adverse effect of spreading to other parts of the body, which could cause muscle weakness, swallowing difficulties, pneumonia, speech disorders and breathing problems.^[42][43]

In April 2009, the FDA updated its mandatory boxed warning cautioning that the effects of the botulinum toxin may spread from the area of injection to other areas of the body, causing symptoms similar to those of botulism, and that these adverse reactions, which were more likely in cases ignoring approved use guidance and label directions, could result in patient death (see above).^[5]

Mechanism of action

The toxin produced by Clostridum species is a two-chain protein composed of a 100-kDa heavy chain polypeptide joined via disulfide bond to a 50-kDa light chain polypeptide.^[45] The seven^[46] serologically distinct toxin types possessing different tertiary structures and significant sequence divergence are designated A to G;^[45] six of the seven have subtypes, and five further subtypes of target molecules of botulinum A have been described. The A, B, and E serotypes cause human botulism, with the activities of types A and B enduring longest in vivo (from several weeks to months).^[45]

The terminals of specific axons must internalize the toxin to cause paralysis, and the heavy chain of the toxins is implicated in targeting the toxin to such axon terminals; following the attachment of the toxin heavy chain to proteins on the surface of the terminals, toxin molecules enter the neurons by endocytosis.^[45] The light chain, which has zinc metalloprotease activity,^[45] is released from the endocytotic vesicles and reaches the cytoplasm. Specific serotypes of the toxin cleave synaptosomal-associated protein (25 kDa) (SNAP-25), a protein from the soluble N-ethylmaleimide-sensitive factor attachment receptor (SNARE) family involved in vesicle fusion and mediating release of neurotransmitter, in particular acetylcholine, from axon endings.^[45][47] Cleavage of the SNARE proteins inhibits release of acetylcholine.^[45] Hence, botulinum toxins A, B, and E specifically cleave SNAREs, preventing "neurosecretory vesicles" from docking/fusing with the interior surface of the plasma membrane of the nerve synapse, and so block release of neurotransmitter. In inhibiting acetylcholine release, nerve impulses are blocked, causing the flaccid (sagging) paralysis of muscles characteristic of botulism^[45] (in contrast to the distinct spastic paralysis seen in tetanus).^[48]

History

In 1820, Justinus Kerner, a small-town German medical officer and romantic poet, gave the first complete description of clinical botulism based on extensive clinical observations of so-called “sausage poisoning”.^[49] Following experiments on animals and on himself, he concluded that the toxin acts by interrupting signal transmission in the somatic and autonomic motor systems, without affecting sensory signals or mental functions. He observed that the toxin develops under anaerobic conditions, and can be lethal in minute doses.^[50] His prescience in suggesting that the toxin might be used therapeutically to block both abnormal movements and hypersecretions earned him recognition as the intellectual founder of modern botulinum toxin therapy.^[51]

Seventy-five years later, Émile van Ermengem, professor of bacteriology and a student of Robert Koch, correctly described Clostridium botulinum as the bacterial source of the toxin. Thirty-four attendees at a funeral were poisoned by eating partially salted ham, an extract of which was found to cause botulism-like paralysis in laboratory animals. Van Ermengem isolated and grew the bacterium, and described its toxin,^[52] which was later purified by P Tessmer Snipe and Hermann Sommer.^[53]

Over the next three decades, as food canning was approaching a billion dollar a year industry, botulism was becoming a public health hazard. Karl Friedrich Meyer, a prodigiously productive Swiss-American veterinary scientist (and supervisor of Alan B. Scott’s mother’s 1925 MA degree in bacteriology), created a center at the Hooper Foundation in San Francisco, where he developed techniques for growing the organism and extracting the toxin, and conversely, for preventing organism growth and toxin production, and inactivating the toxin by heating. The California canning industry was thereby preserved.

With the outbreak of World War II, weaponization of botulinum toxin was investigated at Fort Detrick in Maryland. Carl Lamanna and James Duff ^[54] developed the concentration and crystallization techniques that Edward J Schantz used to create the first clinical product. When the Army’s Chemical Corps was disbanded, Schantz moved to the Food Research Institute in Wisconsin, where he manufactured toxin for experimental use and generously provided it to the academic community.

The mechanism of botulinum toxin action – blocking the release from nerve endings of the neurotransmitter acetylcholine – was elucidated in the mid-1900s,^[55] and remains an important research topic. Nearly all toxin treatments are based on this effect in various body tissues.

Eye muscle disorders

Ophthalmologists specializing in eye muscle disorders (strabismus) had developed the method of EMG-guided injection (using the electromyogram, the electrical signal from an activated muscle, to guide injection) of local anesthetics as a diagnostic technique for evaluating an individual muscle’s contribution to an eye movement.^[56] Because strabismus surgery frequently needed repeating, a search was undertaken for non-surgical, injection treatments using various anesthetics, alcohols, enzymes, enzyme blockers, and snake neurotoxins. Finally, inspired by Daniel Drachman’s work with chicks at Johns Hopkins,^[57] Alan B Scott and colleagues injected botulinum toxin into monkey extraocular muscles.^[58] The result was remarkable: a few picograms induced paralysis that was confined to the target muscle, long in duration, and without side-effects.

After working out techniques for freeze-drying, buffering with albumin, and assuring sterility, potency, and safety, Scott applied to the FDA for investigational drug use, and began manufacturing botulinum type A neurotoxin in his San Francisco lab. He injected the first strabismus patients in 1977, reported its clinical utility in 1980,^[59] and had soon trained hundreds of ophthalmologists in EMG-guided injection of the drug he named Oculinum™ (“eye aligner”).

Strabismus is caused by imbalances in the actions of muscles that rotate the eyes, and can sometimes be relieved by weakening a muscle that pulls too strongly, or pulls against one that has been weakened by disease or trauma. Muscles weakened by toxin injection recover from paralysis after several months, so it might seem that injection would then need to be repeated. However, muscles adapt to the lengths at which they are chronically held,^[60] so that if a paralyzed muscle is stretched by its antagonist, it grows longer, while the antagonist shortens, yielding a permanent effect. If there is good binocular vision, the brain mechanism of motor fusion, which aligns the eyes on a target visible to both, can stabilize the corrected alignment.

Other muscle disorders

By 1982, eye muscles had been injected for strabismus and nystagmus (jerky, involuntary eye movements), eyelid muscles for retraction and blepharospasm (sustained, involuntary contractions of muscles around the eye), facial muscles for hemifacial spasm, and limb muscles for dystonia (sustained muscle spasm), all as predicted in Scott’s 1973 study.^[58]

Scott also injected the first cases of torticollis (painful, spastic twisting of the neck), which were later published by Joseph Tsui of Vancouver.^[61] But even a century and a half after Kerner’s work, it was difficult for many to accept that the specificity and molecular tenacity that made ingested toxin so deadly also made it remarkably safe when injected directly into a target muscle, and no Bay Area neurology, orthopedic, or rehabilitation physician would try toxin for muscle contractures with stroke, dystonia, torticollis, or cerebral palsy. L Andrew Koman of Wake Forest University in North Carolina pioneered use of toxin to treat pediatric leg spasm in cerebral palsy.^[62]

Patient groups quickly spread the word that there were now effective treatments for previously untreatable motility disorders such as blepharospasm, which can result in functional blindness despite an otherwise normal visual system. Torticollis patients discovered that their pain could be markedly reduced by toxin injection, motility increased, head position somewhat improved, even if tremor was not. In 1993, Scott, Pankaj Pasricha, and colleagues showed that botulinum toxin could be used for the treatment of achalasia, a spasm of the lower esophageal sphincter.^[63] Spasmodic dysphonia (difficulty speaking), various gastroenteric and urinary sphincter spasms, muscle spasm in stroke, and many other muscle disorders, were also treated with botulinum toxin injection.

In January 2014, botulinum toxin was approved by UK's Medicines and Healthcare Products Regulatory Agency (MHRA) for treatment of restricted ankle motion due to lower limb spasticity associated with stroke in adults.^[64]

Botulinum toxin has not been approved for pediatric use.^[10] However, it has been used off-label for several pediatric conditions, including infantile esotropia^[65] and spastic conditions in cerebral palsy.

Supply problems

In 1986, Oculinum Inc, Scott's micromanufacturer and distributor of botulinum toxin, was unable to obtain product liability insurance, and could no longer supply the drug. As supplies became exhausted, patients who had come to rely on periodic injections became desperate. For 4 months, as liability issues were resolved, American blepharospasm patients traveled to Canadian eye centers for their injections.^[66]

Based on data from thousands of patients collected by 240 investigators, under the 1983 US Orphan Drug Act, Scott got FDA approval in 1989 to market Oculinum for clinical use in the United States to treat adult strabismus and blepharospasm. Allergan served as the drug’s distributor for almost 2 years, and in 1991 took over the licenses and changed the drug’s name to Botox^®.

Hypersecretion

Finally pursuing Kerner’s suggestion 175 years earlier, Khalafalla Bushara and David Park in England made the first non-muscular use of botulinum toxin in humans with a demonstration that injections could inhibit excess sweating.^[67]

The toxin was also used by Drobik and Laskawi to treat hyperhidrosis in Frey’s Syndrome, in which facial sweating occurs after parotid gland surgery due to anomalous regrowth of injured salivary nerves to the face.^[68] It was a natural extension to use the toxin to ameliorate the poorly handled salivary secretions in amyotrophic lateral sclerosis and to decrease excessive lacrimal gland secretion. The concept of blocking cholinergic innervation to sweat glands as a treatment for hyperhidrosis in the axilla, hands, and elsewhere, followed.

Cosmetics

Richard Clark, a plastic surgeon from Sacramento (CA), was the first to document a cosmetic use for botulinum toxin. He treated facial asymmetry caused by unilateral facial nerve paralysis by injecting toxin into the non-paralyzed frontal muscle.^[69]

Marrying ophthalmology to dermatology, Jean and Alistair Carruthers observed that blepharospasm patients who received injections around the eyes and upper face also enjoyed diminished facial glabellar lines (“frown lines” between the eyebrows), thereby initiating the highly-popular cosmetic use of the toxin.^[70] Brin, and a group at Columbia University under Monte Keen made similar reports.^[71] In 2002, following clinical trials, the FDA approved Botox Cosmetic, botulinum A toxin to temporarily improve the appearance of moderate-to-severe glabellar lines.^[72] The FDA approved a fully in vitro assay for use in the stability and potency testing of Botox® in response to increasing public concern that LD50 testing was required for each batch sold in the market.^[73][74]

Chronic pain

William Binder reported that patients who had cosmetic injections around the face reported relief from chronic headache.^[75] This was initially thought to be an indirect effect of reduced muscle tension, but it is now known that the toxin inhibits release of peripheral nociceptive neurotransmitters, suppressing the central pain processing systems responsible for migraine headache.^[76][77] In 2010, the FDA approved intramuscular botulinum toxin injections for prophylactic treatment of chronic migraine headache.

Society and culture

Economics

As of 2013, botulinum toxin injections are the most common cosmetic operation, with 6.3 million procedures in the United States, according to the American Society of Plastic Surgeons. Qualifications for Botox injectors vary by county, state and country. Botox cosmetic providers include dermatologists, plastic surgeons, aesthetic spa physicians, dentists, nurse practitioners, nurses and physician assistants.

The global market for botulinum toxin products, driven by their cosmetic applications, is forecast to reach $2.9 billion by 2018. The facial aesthetics market, of which they are a component, is forecast to reach $4.7 billion ($2 billion in the U.S.) in the same timeframe.^[78]

Bioterrorism

Botulinum toxin has been recognized as a potential agent for use in bioterrorism.^[79] It can be absorbed through the eyes, mucous membranes, respiratory tract, or non-intact skin.^[80]

The effects of botulinum toxin are different from those of nerve agents involved insofar in that botulism symptoms develop relatively slowly (over several days), while nerve agent effects are generally much more rapid and can be instantaneous. Evidence suggests that nerve exposure (simulated by injection of atropine and pralidoxime) will increase mortality by enhancing botulinum toxin's mechanism of toxicity.

With regard to detection, current protocols using NBC detection equipment (such as M-8 paper or the ICAM) will not indicate a "positive" when samples containing botulinum toxin are tested. To confirm a diagnosis of botulinum toxin poisoning, therapeutically or to provide evidence in death investigations, botulinum toxin may be quantitated by immunoassay of human biological fluids; serum levels of 12–24 mouse LD₅₀ units per milliliter have been detected in poisoned patients.^[81]

Brand names

Botulinum toxin A is marketed under the brand names Botox (marketed by Allergan), Dysport (marketed by Ipsen), and Xeomin (marketed by Merz Pharma). Botulinum toxin B is marketed under the brand name Myobloc (marketed by Solstice Neurosciences).

In the United States, botulinum toxin products are manufactured by a variety of companies, for both therapeutic and cosmetic use. Allergan, Inc., a principal U.S. supplier through their Botox products, reported in its company materials in 2011 that it could "supply the world's requirements for 25 indications approved by Government agencies around the world" with less than one gram of raw botulinum toxin.^[82] Myobloc or Neurobloc, a botulinum toxin type B product, is produced by Solstice Neurosciences, a subsidiary of US WorldMeds. Dysport, a therapeutic formulation of the type A toxin manufactured by Galderma in the United Kingdom, is licensed for the treatment of focal dystonias and certain cosmetic uses in the U.S. and other countries.^[83]

After the three primary U.S. manufacturers, there many reports of other sources of production. Xeomin, manufactured in Germany by Merz, is also available for both therapeutic and cosmetic use in the U.S.^[84] Lanzhou Institute of Biological Products in China manufactures a BTX-A product; as of 2014 it was the only BTX-A approved in China.^[84] BTX-A is also sold as Lantox and Prosigne on the global market.^[85] Neuronox, a BTX-A product, was introduced by Medy-Tox Inc. of South Korea in 2009;^[86] Neuronox is also markets as Siax in the U.S.

Toxin production

Botulism toxins are produced by bacteria of the genus Clostridium, namely Clostridium botulinum, C. butyricum, C. baratii and C. argentinense,^[87] which are widely distributed, including in soil and dust. As well, the bacteria can be found inside homes on floors, carpet, and countertops even after cleaning. Some food products such as honey can contain amounts of the bacteria.

Food-borne botulism results, indirectly, from ingestion of food contaminated with Clostridium spores, where exposure to an anaerobic environment allows the spores to germinate, after which the bacteria can multiply and produce toxin. Critically, it is ingestion of toxin rather than spores or vegetative bacteria that causes botulism. Botulism is nevertheless known to be transmitted through canned foods not cooked correctly before canning or after can opening, and so is preventable. Infant botulism cases arise chiefly as a result of environmental exposure and are therefore more difficult to prevent. Infant botulism arising from consumption of honey can be prevented by eliminating honey from diets of children less than 12 months old.^[88]

Therapeutic and weaponisable forms of the toxin are sourced from strains of Clostriudium where both the growth and toxin isolation are under specialized conditions.

Organism and toxin susceptibilities

Proper refrigeration at temperatures below 3 °C (38 °F) retards the growth of Clostridium botulinum. The organism is also susceptible to high salt, high oxygen, and low pH levels. The toxin itself is rapidly destroyed by heat, such as in thorough cooking.^[89] The spores that produce the toxin are heat-tolerant and will survive boiling water for an extended period of time.^[90]

The botulinum toxin is denatured and thus deactivated at temperatures greater than 80 °C (176 °F).^[91] As a zinc metalloprotease (see below), the toxin's activity is also susceptible, post-exposure, to inhibition by protease inhibitors, e.g., zinc-coordinating hydroxamates.^[45][92]

Research

Blepharospasm and strabismus

In the early 1980s, university-based ophthalmologists in the USA and Canada further refined the use of botulinum toxin as a therapeutic agent. By 1985, a scientific protocol of injection sites and dosage had been empirically determined for treatment of blepharospasm and strabismus.^[93] Side effects in treatment of this condition were deemed to be rare, mild and treatable.^[94] The beneficial effects of the injection lasted only 4–6 months. Thus, blepharospasm patients required re-injection two or three times a year.

In 1986, Scott's micromanufacturer and distributor of Botox was no longer able to supply the drug because of an inability to obtain product liability insurance. Patients became desperate, as supplies of Botox were gradually consumed, forcing him to abandon patients who would have been due for their next injection. For a period of four months, American blepharospasm patients had to arrange to have their injections performed by participating doctors at Canadian eye centers until the liability issues could be resolved.^[66]

In December 1989, Botox, manufactured by Allergan, Inc., was approved by the US Food and Drug Administration (FDA) for the treatment of strabismus, blepharospasm, and hemifacial spasm in patients over 12 years old.^[95]

Botox has not been approved for any pediatric use.^[10] It has, however, been used off-label by physicians for several conditions. including spastic conditions in pediatric patients with cerebral palsy, a therapeutic course that has resulted in patient deaths.^[10] In the case of treatment of infantile esotropia in patients younger than 12 years of age, several studies have yielded differing results.^[65]

Cosmetic

The cosmetic effect of BTX-A on wrinkles was originally documented by a plastic surgeon from Sacramento, California, Richard Clark, and published in the journal Plastic and Reconstructive Surgery in 1989.^[69] Canadian husband and wife ophthalmologist and dermatologist physicians, JD and JA Carruthers, were the first to publish a study on BTX-A for the treatment of glabellar frown lines in 1992.^[96] Similar effects had reportedly been observed by a number of independent groups (Brin, and the Columbia University group under Monte Keen.^[71]) After formal trials, on April 12, 2002, the FDA announced regulatory approval of botulinum toxin type A (Botox Cosmetic) to temporarily improve the appearance of moderate-to-severe frown lines between the eyebrows (glabellar lines).^[72] Subsequently, cosmetic use of botulinum toxin type A has become widespread.^[97] The results of Botox Cosmetic can last up to four months and may vary with each patient.^[98] The US Food and Drug Administration approved an alternative product-safety testing method in response to increasing public concern that LD50 testing was required for each batch sold in the market.^[73][74]

Upper motor neuron syndrome

BTX-A is now a common treatment for muscles affected by the upper motor neuron syndrome (UMNS), such as cerebral palsy, for muscles with an impaired ability to effectively lengthen. Muscles affected by UMNS frequently are limited by weakness, loss of reciprocal inhibition, decreased movement control and hypertonicity (including spasticity). In January 2014, Botulinum toxin was approved by UK's Medicines and Healthcare Products Regulatory Agency (MHRA) for the treatment of ankle disability due to lower limb spasticity associated with stroke in adults.^[64] Joint motion may be restricted by severe muscle imbalance related to the syndrome, when some muscles are markedly hypertonic, and lack effective active lengthening. Injecting an overactive muscle to decrease its level of contraction can allow improved reciprocal motion, so improved ability to move and exercise.

Sweating

As noted, Bushara and Park were the first to demonstrate a nonmuscular use of BTX-A while treating patients with hemifacial spasm in England in 1993, showing that botulinum toxin injections inhibit sweating, and so are useful in treating hyperhidrosis (excessive sweating).^[67] BTX-A has since been approved for the treatment of severe primary axillary hyperhidrosis (excessive underarm sweating of unknown cause), which cannot be managed by topical agents.^[15][16]

Cervical dystonia

BTX-A is commonly used to treat cervical dystonia, but it can become ineffective after a time. Botulinum toxin type B (BTX-B) received FDA approval for treatment of cervical dystonia on December 21, 2000. Trade names for BTX-B are Myobloc in the United States, and Neurobloc in the European Union.^[84]

Chronic migraine

Onabotulinumtoxin A (trade name Botox) received FDA approval for treatment of chronic migraines on October 15, 2010. The toxin is injected into the head and neck to treat these chronic headaches. Approval followed evidence presented to the agency from two studies funded by Allergan, Inc. showing a very slight improvement in incidence of chronic migraines for migraine sufferers undergoing the Botox treatment.^[99][100]

Since then, several randomized control trials have shown botulinum toxin type A to improve headache symptoms and quality of life when used prophylactically for patients with chronic migraine^[101] who exhibit headache characteristics consistent with: pressure perceived from outside source, shorter total duration of chronic migraines (<30 years), "detoxification" of patients with coexisting chronic daily headache due to medication overuse, and no current history of other preventive headache medications.^[102]

See also

• Microbial toxins

References

External links

• A Poison that can Heal from the U.S. Food and Drug Administration
• Does Botox get into the brain? Troubling research contradicts earlier findings about the treatment
• Government backs vital plans to make Botox safer
• BotDB: extensive resources on BoNT structures, inhibitors, kinetics, and literature
• A consumer sociological investigation of Botox Cosmetic's Rise

Skeletal muscle relaxants (M03) Peripherally acting (primarily antinicotinic, NMJ block) Non-depolarizing Curare alkaloids Alcuronium Dimethyltubocurarine Tubocurarine 4° ammonium agents ultra-short duration: Gantacurium short duration: Mivacurium Chandonium intermediate duration: Atracurium Cisatracurium Fazadinium Rocuronium Vecuronium long duration: Doxacurium Dimethyltubocurarine Pancuronium Pipecuronium Laudexium Gallamine unsorted: Hexafluronium (Hexafluorenium) Depolarizing Choline derivatives: Suxamethonium (Succinylcholine) Polyalkylene derivatives: Hexamethonium ACh release inhibitors Botulinum toxin Centrally acting Carbamic acid esters Carisoprodol Cyclarbamate Difebarbamate Febarbamate Meprobamate Phenprobamate Styramate Tybamate Benzodiazepines Bromazepam Diazepam Clonazepam Flunitrazepam Lorazepam Nitrazepam Temazepam Tetrazepam Nonbenzodiazepines Eszopiclone Thienodiazepines Etizolam Quinazolines Methaqualone Anticholinergics (Antimuscarinics) Cyclobenzaprine Orphenadrine Other Arbaclofen placarbil Baclofen Chlormezanone Chlorphenesin Chlorzoxazone Donepezil Eperisone Fenyramidol Flopropione Gabapentin GHB Mephenesin Mephenoxalone Metaxalone Methocarbamol Phenibut Pregabalin Pridinol Promoxolane Quinine Thiocolchicoside Tizanidine Tolperisone Directly acting Dantrolene

Toxins enterotoxin neurotoxin hemotoxin cardiotoxin phototoxin Bacterial toxins Exotoxin Gram positive Bacilli Clostridium: tetani Tetanospasmin Tetanolysin perfringens Alpha toxin Enterotoxin difficile A B botulinum Botox other: Anthrax toxin Listeriolysin O Cocci Streptolysin Leukocidin Panton-Valentine leukocidin Staphylococcus Staphylococcus aureus alpha/beta/delta Exfoliatin Toxic shock syndrome toxin Staphylococcal Enterotoxin B (SEB) Actinobacteria Cord factor Diphtheria toxin Gram negative Shiga toxin Verotoxin/shiga-like toxin (E. coli) E. coli heat-stable enterotoxin/enterotoxin Cholera toxin Pertussis toxin Pseudomonas exotoxin Extracellular adenylate cyclase Mechanisms type I Superantigen type II Pore-forming toxin type III AB toxin/AB5 Endotoxin Lipopolysaccharide Lipid A Bacillus thuringiensis delta endotoxin Virulence factor Clumping factor A Fibronectin binding protein A Mycotoxins Aflatoxin Amatoxin (alpha-amanitin, beta-amanitin, gamma-amanitin, epsilon-amanitin) beta-Nitropropionic acid Citrinin Cytochalasin Ergotamine Fumonisin (Fumonisin B1, Fumonisin B2) Gliotoxin Ibotenic acid Muscimol Ochratoxin Patulin Phalloidin Sterigmatocystin Trichothecene Vomitoxin Zeranol Zearalenone Plant toxins Amygdalin Anisatin Antiarin Brucine Chaconine Cicutoxin Daphnin Delphinine Divicine Djenkolic acid Falcarinol Gossypol Helenalin Ledol Linamarin Lotaustralin Mimosine Oenanthotoxin Oleandrin Persin Protoanemonin Pseudaconitine Retronecine Resiniferatoxin Scopolamine Solamargine Solanidine Solanine Solasodamine Solasodine Solasonine Solauricidine Solauricine Strychnine Swainsonine Tagetitoxin Tinyatoxin Tomatine Toxalbumin Abrin Ricin Tutin Invertebrate toxins scorpion: Androctonus australis hector insect toxin Charybdotoxin Maurotoxin Agitoxin Margatoxin Slotoxin Scyllatoxin Hefutoxin Lq2 Birtoxin Bestoxin BmKAEP Phaiodotoxin Imperatoxin Pi3 spider: Latrotoxin Alpha-latrotoxin CSTX Cupiennins PhTx3 Stromatoxin Vanillotoxin Huwentoxin mollusca: Conotoxin Eledoisin Onchidal Saxitoxin Tetrodotoxin Vertebrate toxins fish: Ciguatera Tetrodotoxin amphibian: (+)-Allopumiliotoxin 267A Batrachotoxin Bufotoxins Arenobufagin Bufotalin Bufotenin Cinobufagin Marinobufagin Epibatidine Histrionicotoxin Pumiliotoxin 251D Samandarin Samandaridine Tarichatoxin reptile/snake venom: Bungarotoxin Alpha-Bungarotoxin Beta-Bungarotoxin Calciseptine Taicatoxin Calcicludine Cardiotoxin III note: some toxins are produced by lower species and pass through intermediate species Category Commons WikiProject

Cholinergics   Receptor ligands mACh Agonists: 77-LH-28-1 AC-42 AC-260,584 Aceclidine Acetylcholine AF30 AF150(S) AF267B AFDX-384 Alvameline AQRA-741 Arecoline Bethanechol Butyrylcholine Carbachol CDD-0034 CDD-0078 CDD-0097 CDD-0098 CDD-0102 Cevimeline Choline cis-Dioxolane Ethoxysebacylcholine Itameline LY-593,039 L-689,660 LY-2,033,298 McNA343 Methacholine Milameline Muscarine NGX-267 Ocvimeline Oxotremorine PD-151,832 Pilocarpine RS86 Sabcomeline SDZ 210-086 Sebacylcholine Suberyldicholine Talsaclidine Tazomeline Thiopilocarpine Vedaclidine VU-0029767 VU-0090157 VU-0152099 VU-0152100 VU-0238429 WAY-132,983 Xanomeline YM-796 Antagonists: 3-Quinuclidinyl benzilate 4-DAMP Aclidinium bromide Anisodamine Anisodine Antihistamines (first-generation) (e.g., brompheniramine, chlorphenamine, cyproheptadine, dimenhydrinate, diphenhydramine, doxylamine, mepyramine (pyrilamine), phenindamine, pheniramine, promethazine, tripelennamine, triprolidine) Atropine Atropine methonitrate Atypical antipsychotics (e.g., clozapine, olanzapine, quetiapine, zotepine) Benactyzine Benzatropine (benztropine) Benzilylcholine mustard Benzydamine BIBN 99 Biperiden Bornaprine CAR-226,086 CAR-301,060 CAR-302,196 CAR-302,282 CAR-302,368 CAR-302,537 CAR-302,668 CS-27349 Cyclobenzaprine Cyclopentolate Darifenacin DAU-5884 Dimethindene Dexetimide DIBD Dicyclomine (dicycloverine) Ditran EA-3167 EA-3443 EA-3580 EA-3834 Etanautine Etybenzatropine (ethybenztropine) Flavoxate Himbacine HL-031,120 Ipratropium bromide J-104,129 Hyoscyamine Mamba toxin 3 Mamba toxin 7 Mazaticol Mebeverine Methoctramine Metixene N-Ethyl-3-piperidyl benzilate N-Methyl-3-piperidyl benzilate Orphenadrine Otenzepad Oxybutynin PBID PD-102,807 PD-0298029 Phenglutarimide Phenyltoloxamine Pirenzepine Piroheptine Procyclidine Profenamine RU-47,213 SCH-57,790 SCH-72,788 SCH-217,443 Scopolamine (hyoscine) Solifenacin Telenzepine Tetracyclic antidepressants (e.g., amoxapine, maprotiline, mianserin, mirtazapine) Tiotropium bromide Tolterodine Tricyclic antidepressants (e.g., amitriptyline, butriptyline, clomipramine, desipramine, dosulepin (dothiepin), doxepin, imipramine, lofepramine, nortriptyline, protriptyline, trimipramine) Trihexyphenidyl Tripitamine Tropatepine Tropicamide Typical antipsychotics (e.g., chlorpromazine, loxapine, thioridazine) WIN-2299 Xanomeline Zamifenacin nACh Agonists: 5-HIAA A-84,543 A-366,833 A-582,941 A-867,744 ABT-202 ABT-418 ABT-560 ABT-894 Acetylcholine Altinicline Anabasine Anatoxin-a AR-R17779 Butinoline Butyrylcholine Carbachol Choline Cotinine Cytisine Decamethonium Desformylflustrabromine Dianicline Dimethylphenylpiperazinium Epibatidine Epiboxidine Ethanol Ethoxysebacylcholine EVP-4473 EVP-6124 Galantamine GTS-21 Ispronicline Ivermectin Levamisole Lobeline MEM-63,908 (RG-3487) Morantel Nicotine (tobacco) NS-1738 PHA-543,613 PHA-709,829 PNU-120,596 PNU-282,987 Pozanicline Rivanicline RJR-2429 Sazetidine A SB-206553 Sebacylcholine SIB-1508Y SIB-1553A SSR-180,711 Suberyldicholine Suxamethonium (succinylcholine) TC-1698 TC-1734 TC-1827 TC-2216 TC-5214 TC-5619 TC-6683 Tebanicline Tropisetron UB-165 Varenicline WAY-317,538 XY-4083 Antagonists: 18-MAC 18-MC α-Neurotoxins (e.g., α-bungarotoxin, α-cobratoxin, α-conotoxin, many others) ABT-126 Alcuronium Allopregnanolone Amantadine Anatruxonium AQW051 Atracurium Barbiturates (e.g., pentobarbital, sodium thiopental) Bungarotoxins (e.g., α-bungarotoxin, κ-bungarotoxin) Bupropion Chandonium Chlorisondamine Cisatracurium Coclaurine Coronaridine Cyclopropane Dacuronium Decamethonium Dehydronorketamine Desflurane Dextromethorphan Dextropropoxyphene Dextrorphan Diadonium DHβE Dihydrochandonium Dimethyltubocurarine (metocurine) Dipyrandium Dizocilpine (MK-801) Doxacurium Encenicline Enflurane Esketamine Fazadinium Gallamine Halothane Hexafluronium Hexamethonium (benzohexonium) Hydroxybupropion Hydroxynorketamine Ibogaine Isoflurane Ketamine Kynurenic acid Laudexium (laudolissin) Levacetylmethadol Levomethadone Malouetine ME-18-MC Mecamylamine Memantine Methadone Methorphan (racemethorphan) Methyllycaconitine Metocurine Mivacurium Morphanol (racemorphan) Neramexane Nitrous oxide Norketamine Pancuronium bromide Pempidine Pentamine Pentolinium Phencyclidine Pipecuronium Progesterone Promegestone Radafaxine Rapacuronium Reboxetine Rocuronium Sevoflurane Surugatoxin Thiocolchicoside Toxiferine Tramadol Trimetaphan camsilate (trimethaphan camsylate) Tropeinium Tubocurarine Vanoxerine Vecuronium Xenon   Transporter ligands CHT Inhibitors: Hemicholinium-3 (hemicholine) Triethylcholine Enhancers: Coluracetam VAChT Inhibitors: Vesamicol   Enzyme modulators ChAT Inhibitors: 1-(-Benzoylethyl)pyridinium 2-(α-Naphthoyl)ethyltrimethylammonium 3-Chloro-4-stillbazole 4-(1-Naphthylvinyl)pyridine Acetylseco hemicholinium-3 Acryloylcholine AF64A B115 BETA CM-54,903 N,N-Dimethylaminoethylacrylate N,N-Dimethylaminoethylchloroacetate AChE Inhibitors: Reversible: Carbamates: Aldicarb Bendiocarb Bufencarb Caffeine Carbaryl Carbendazim Carbetamide Carbofuran Chlorbufam Chloropropham Ethienocarb Ethiofencarb Fenobucarb Fenoxycarb Formetanate Furadan Ladostigil Methiocarb Methomyl Miotine Oxamyl Phenmedipham Pinmicarb Pirimicarb Propamocarb Propham Propoxur; Stigmines: Distigmine bromide Eptastigmine Ganstigmine Neostigmine Phenserine Physostigmine Pyridostigmine bromide Quilostigmine Rivastigmine Terestigmine; Others: Acotiamide Ambenonium Donepezil Caffeine Edrophonium Galantamine Huperzine A Ipidacrine Minaprine Tacrine Zanapezil Irreversible: Organophosphates: Acephate Azinphos-methyl Bensulide Cadusafos Chlorethoxyfos Chlorfenvinphos Chlorpyrifos Chlorpyrifos-methyl Coumaphos Cyclosarin Demeton Demeton-S-methyl Diazinon Dichlorvos Dicrotophos Diisopropyl fluorophosphate Diisopropylphosphate Dimethoate Dioxathion Disulfoton EA-3148 Echothiophate Ethion Ethoprop Fenamiphos Fenitrothion Fenthion Fosthiazate GV Isofluorophate Isoxathion Malaoxon Malathion Methamidophos Methidathion Metrifonate Mevinphos Monocrotophos Naled Novichok agent Omethoate Oxydemeton-methyl Paraoxon Parathion Parathion-methyl Phorate Phosalone Phosmet Phoxim Pirimiphos-methyl Sarin Soman Tabun Tebupirimfos Temefos Terbufos Tetrachlorvinphos Tribufos Trichlorfon VE VG VM VR VX; Others: Demecarium Fasciculins (green mamba toxins) (1, 2, 3, 4) Onchidal (Onchidella binneyi) Reactivators: Asoxime Obidoxime Pralidoxime BChE Inhibitors: Cymserine Many of the AChE inhibitors listed above   Release modulators Inhibitors SNAP-25 inactivators: Botulinum toxin (A, C, E) VAMP inactivators: Botulinum toxin (B, D, F, G) Others: Bungarotoxins (β-bungarotoxin, γ-bungarotoxin) Enhancers LPHN agonists: α-Latrotoxin Others: Atracotoxin (e.g., robustoxin, versutoxin) Crotoxin   Others Precursors Choline (lecithin) Citicoline Cyprodenate Dimethylethanolamine Glycerophosphocholine Meclofenoxate (centrophenoxine) Phosphatidylcholine Phosphatidylethanolamine Phosphorylcholine Pirisudanol Cofactors Acetic acid Acetylcarnitine Acetyl-coA Vitamin B5

Cosmetics Face Anti-aging cream Botox BB cream Concealer Cleanser Facial Facial toning Foundation Moisturizer Permanent makeup Primer Powder Rouge Skin whitening Toner Veil Lips Gloss Liner Lipstick Plumper Stain Eyes Circle contact lens Eyelash extensions Eyelid glue Eye liner Eye shadow Kohl Mascara Hair Conditioner Removal chemical electric laser IPL plucking shaving threading waxing Shampoo Styling Styling products gel mousse pomade spray wax Nails Artificial nails Buffing Manicure Nail polish Pedicure Body Body powder Cold cream Cosmetic surgery Peeling Related topics Cosmetic electrotherapy Cosmetic ingredients Cosmetics advertising Cosmetology History of cosmetics   Major cosmetic brands Ahava Almay AmorePacific Artistry Aveda Avon Bath & Body Works Benefit Biotherm Bobbi Brown The Body Shop Bonne Bell Bumble and bumble Burt's Bees Cargo Carol's Daughter Ciaté Clarins Clinique Coty CoverGirl Creme 21 Cutex Daigaku Honyaku Center Elizabeth Arden Estée Lauder Eyes Lips Face Faberge Hard Candy Helena Rubinstein Kao Corporation Kevyn Aucoin Kiehl's La Mer Lancôme Laneige Laura Mercier Laura Mercier Cosmetics Lise Watier L'Oréal L'occitane Love Cosmetics Lush MAC Cosmetics Mary Kay Max Factor Maybelline ModelCo Molton Brown NARS Natura Natural Wonder Neal's Yard Remedies Neutrogena Nexxus Nivea O Boticário OPI Oriflame Origins Paula Begoun Pond's Creams Red Earth Revlon Richard Hudnut Rimmel Sephora Shiseido Shu Uemura SK-II SkinCeuticals Stila ULTA Beauty Ultima II Urban Decay Vichy Victoria's Secret Wella Yves Rocher Categories Companies People History

Proteases: metalloendopeptidases (EC 3.4.24) ADAM proteins Alpha secretases ADAM9 ADAM10 ADAM17 ADAM19 ADAM2 ADAM7 ADAM8 ADAM11 ADAM12 ADAM15 ADAM18 ADAM22 ADAM23 ADAM28 ADAM33 ADAMTS1 ADAMTS2 ADAMTS3 ADAMTS4 ADAMTS5 ADAMTS8 ADAMTS9 ADAMTS10 ADAMTS12 ADAMTS13 Matrix metalloproteinases Collagenases MMP1 MMP8 Gelatinases MMP2 MMP9 MMP3 MMP7 MMP10 MMP11 MMP12 MMP13 MMP14 MMP15 MMP16 MMP17 MMP19 MMP20 MMP21 MMP23A MMP23B MMP24 MMP25 MMP26 MMP27 MMP28 Other Neprilysin Procollagen peptidase Thermolysin Pregnancy-associated plasma protein A Bone morphogenetic protein 1 Lysostaphin Insulin-degrading enzyme ZMPSTE24

Proteins: enzymes Activity Active site Binding site Catalytic triad Oxyanion hole Enzyme promiscuity Catalytically perfect enzyme Coenzyme Cofactor Enzyme catalysis Enzyme kinetics Lineweaver–Burk plot Michaelis–Menten kinetics Regulation Allosteric regulation Cooperativity Enzyme inhibitor Classification EC number Enzyme superfamily Enzyme family List of enzymes Types EC1 Oxidoreductases(list) EC2 Transferases(list) EC3 Hydrolases(list) EC4 Lyases(list) EC5 Isomerases(list) EC6 Ligases(list)