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Friday, December 24, 2021

Poison dart frog

From Wikipedia, the free encyclopedia

Poison dart frogs (Dendrobatidae)
Blue-poison.dart.frog.and.Yellow-banded.dart.frog.arp.jpg
Dendrobates tinctorius "azureus" (top) and Dendrobates leucomelas (bottom).

 
Scientific classification 
Kingdom: Animalia
Phylum: Chordata
Class: Amphibia
Order: Anura
Superfamily: Dendrobatoidea
Family: Dendrobatidae
Cope, 1865
Subfamilies and genera
Dendrobatidae range.PNG
Distribution of Dendrobatidae (in black)

Poison dart frog (also known as dart-poison frog, poison frog or formerly known as poison arrow frog) is the common name of a group of frogs in the family Dendrobatidae which are native to tropical Central and South America. These species are diurnal and often have brightly colored bodies. This bright coloration is correlated with the toxicity of the species, making them aposematic. Some species of the family Dendrobatidae exhibit extremely bright coloration along with high toxicity, while others have cryptic coloration with minimal to no amount of observed toxicity. The species that have great toxicity derive this from their diet of ants, mites and termites. Other species however, that exhibit cryptic coloration and low to no amounts of toxicity, eat a much larger variety of prey. Many species of this family are threatened due to human infrastructure encroaching on their habitats.

These amphibians are often called "dart frogs" due to the Native Americans' use of their toxic secretions to poison the tips of blowdarts. However, of over 170 species, only four have been documented as being used for this purpose (curare plants are more commonly used), all of which come from the genus Phyllobates, which is characterized by the relatively large size and high levels of toxicity of its members.

Characteristics

Dyeing dart frog (Dendrobates tinctorius)

Most species of poison dart frogs are small, sometimes less than 1.5 cm (0.59 in) in adult length, although a few grow up to 6 cm (2.4 in) in length. They weigh 1 oz. on average. Most poison dart frogs are brightly colored, displaying aposematic patterns to warn potential predators. Their bright coloration is associated with their toxicity and levels of alkaloids. For example, frogs of the genus Dendrobates have high levels of alkaloids, whereas Colostethus species are cryptically colored and are not toxic.

Poison dart frogs are an example of an aposematic organism. Their bright coloration advertises unpalatability to potential predators. Aposematism is currently thought to have originated at least four times within the poison dart family according to phylogenetic trees, and dendrobatid frogs have since undergone dramatic divergences – both interspecific and intraspecific – in their aposematic coloration. This is surprising given the frequency-dependent nature of this type of defense mechanism.

Adult frogs lay their eggs in moist places, including on leaves, in plants, among exposed roots, and elsewhere. Once the eggs hatch, the adult piggybacks the tadpoles, one at a time, to suitable water, either a pool, or the water gathered in the throat of bromeliads or other plants. The tadpoles remain there until they metamorphose, in some species fed by unfertilized eggs laid at regular intervals by the mother.

Habitat

Poison dart frogs are endemic to humid, tropical environments of Central and South America. These frogs are generally found in tropical rainforests, including in Bolivia, Costa Rica, Brazil, Colombia, Ecuador, Venezuela, Suriname, French Guiana, Peru, Panama, Guyana, Nicaragua, and Hawaii (introduced).

Natural habitats include subtropical and tropical, moist, lowland forests, subtropical or tropical high-altitude shrubland, subtropical or tropical, moist, montanes and rivers, freshwater marshes, intermittent freshwater marshes, lakes and swamps. Other species can be found in seasonally wet or flooded lowland grassland, arable land, pastureland, rural gardens, plantations, moist savanna and heavily degraded former forest. Premontane forests and rocky areas have also been known to hold frogs. Dendrobatids tend to live on or close to the ground, but also in trees as much as 10 m (33 ft) from the ground.

Reproduction

Ranitomeya imitator's developmental life stages

Many species of poison dart frogs are dedicated parents. Many poison dart frogs in the genera Oophaga and Ranitomeya carry their newly hatched tadpoles into the canopy; the tadpoles stick to the mucus on the backs of their parents. Once in the upper reaches of the rainforest trees, the parents deposit their young in the pools of water that accumulate in epiphytic plants, such as bromeliads. The tadpoles feed on invertebrates in their nursery, and their mother will even supplement their diet by depositing eggs into the water. Other poison frogs lay their eggs on the forest floor, hidden beneath the leaf litter. Poison frogs fertilize their eggs externally; the female lays a cluster of eggs and a male fertilizes them afterward, in the same manner as most fish. Poison frogs can often be observed clutching each other, similar to the manner most frogs copulate. However, these demonstrations are actually territorial wrestling matches. Both males and females frequently engage in disputes over territory. A male will fight for the most prominent roosts from which to broadcast his mating call; females fight over desirable nests, and even invade the nests of other females to devour competitor's eggs.

The operational sex ratio in the poison dart frog family is mostly female biased. This leads to a few characteristic behaviors and traits found in organisms with an uneven sex ratio. In general, females have a choice of mate. In turn, males show brighter coloration, are territorial, and are aggressive toward other males. Females select mates based on coloration (mainly dorsal), calling perch location, and territory.

Taxonomy

Dart frogs are the focus of major phylogenetic studies, and undergo taxonomic changes frequently. The family Dendrobatidae currently contains 16 genera, with about 200 species.

Genus name and authority Common name Species
Adelphobates (Grant, et al., 2006)
3
Andinobates (Twomey, Brown, Amézquita & Mejía-Vargas, 2011)
15
Ameerega (Bauer, 1986)
30
Colostethus (Cope, 1866) Rocket frogs
15
Dendrobates (Wagler, 1830) Poison dart frogs
5
Ectopoglossus (Grant, Rada, Anganoy-Criollo, Batista, Dias, Jeckel, Machado, and Rueda-Almonacid, 2017)
7
Epipedobates (Myers, 1987) Phantasmal poison frogs
8
Excidobates (Twomey and Brown, 2008)
3
Leucostethus Grant, Rada, Anganoy-Criollo, Batista, Dias, Jeckel, Machado, and Rueda-Almonacid, 2017
6
Hyloxalus (Jiménez de la Espada, 1870)
60
Minyobates (Myers, 1987)
1
Oophaga (Bauer, 1994)
12
Paruwrobates (Bauer, 1994)
3
Phyllobates (Duméril and Bibron, 1841) Golden poison frogs
5
Ranitomeya (Bauer, 1986) Thumbnail dart frogs
16
Silverstoneia (Grant, et al., 2006)
8

Color morphs

Some poison dart frogs species include a number of conspecific color morphs that emerged as recently as 6,000 years ago. Therefore, species such as Dendrobates tinctorius, Oophaga pumilio, and Oophaga granulifera can include color pattern morphs that can be interbred (colors are under polygenic control, while the actual patterns are probably controlled by a single locus). Differing coloration has historically misidentified single species as separate, and there is still controversy among taxonomists over classification.

Variation in predation regimens may have influenced the evolution of polymorphism in Oophaga granulifera, while sexual selection appears to have contributed to differentiation among the Bocas del Toro populations of Oophaga pumilio.

Toxicity and medicine

The skin of the phantasmal poison frog contains epibatidine

Many poison dart frogs secrete lipophilic alkaloid toxins such as allopumiliotoxin 267A, batrachotoxin, epibatidine, histrionicotoxin, and pumiliotoxin 251D through their skin. Alkaloids in the skin glands of poison frogs serve as a chemical defense against predation, and they are therefore able to be active alongside potential predators during the day. About 28 structural classes of alkaloids are known in poison frogs. The most toxic of poison dart frog species is Phyllobates terribilis. It is argued that dart frogs do not synthesize their poisons, but sequester the chemicals from arthropod prey items, such as ants, centipedes and mites – the diet-toxicity hypothesis. Because of this, captive-bred animals do not possess significant levels of toxins as they are reared on diets that do not contain the alkaloids sequestered by wild populations. In fact, new studies suggest that the maternal frogs of some species lay unfertilized eggs, which are laced with trace amounts of alkaloids, to feed the tadpoles. This behavior shows that the poisons are introduced from a very young age. Nonetheless, the captive-bred frogs retain the ability to accumulate alkaloids when they are once again provided an alkaloidal diet. Despite the toxins used by some poison dart frogs, some predators have developed the ability to withstand them. One is the snake Erythrolamprus epinephalus, which has developed immunity to the poison.

Chemicals extracted from the skin of Epipedobates tricolor may be shown to have medicinal value. Scientists use this poison to make a painkiller. One such chemical is a painkiller 200 times as potent as morphine, called epibatidine; however, the therapeutic dose is very close to the fatal dose. A derivative ABT-594 developed by Abbott Laboratories, called Tebanicline got as far as Phase II trials in humans, but was dropped from further development due to unacceptable incidence of gastrointestinal side effects. Secretions from dendrobatids are also showing promise as muscle relaxants, heart stimulants and appetite suppressants. The most poisonous of these frogs, the golden poison frog (Phyllobates terribilis), has enough toxin on average to kill ten to twenty men or about ten thousand mice. Most other dendrobatids, while colorful and toxic enough to discourage predation, pose far less risk to humans or other large animals.

Evolution of skin coloration and toxicity

Skin toxicity evolved alongside bright coloration, perhaps preceding it. Toxicity may have relied on a shift in diet to alkaloid-rich arthropods, which likely occurred at least four times among the dendrobatids. Conspicuous coloration in these frogs is further associated with diet specialization, body mass, aerobic capacity, and chemical defense. Either aposematism and aerobic capacity preceded greater resource gathering, making it easier for frogs to go out and gather the ants and mites required for diet specialization, contrary to classical aposematic theory, which assumes that toxicity from diet arises before signaling. Alternatively, diet specialization preceded higher aerobic capacity, and aposematism evolved to allow dendrobatids to gather resources without predation.

Conspicuousness and toxicity may be inversely related, as polymorphic poison dart frogs that are less conspicuous are more toxic than the brightest and most conspicuous species. Energetic costs of producing toxins and bright color pigments lead to potential trade-offs between toxicity and bright coloration, and prey with strong secondary defenses have less to gain from costly signaling. Therefore, prey populations that are more toxic are predicted to manifest less bright signals, opposing the classical view that increased conspicuousness always evolves with increased toxicity.

Prey mobility could also explain the initial development of aposematic signaling. If prey have characteristics that make them more exposed to predators, such as when some dendrobatids shifted from nocturnal to diurnal behavior, then they have more reason to develop aposematism. After the switch, the frogs had greater ecological opportunities, causing dietary specialization to arise. Thus, aposematism is not merely a signaling system, but a way for organisms to gain greater access to resources and increase their reproductive success.

Dietary conservatism (long-term neophobia) in predators could facilitate the evolution of warning coloration, if predators avoid novel morphs for a long enough period of time. Another possibility is genetic drift, the so-called gradual-change hypothesis, which could strengthen weak pre-existing aposematism.

Sexual selection may have played a role in the diversification of skin color and pattern in poison frogs. With female preferences in play, male coloration could evolve rapidly. Sexual selection is influenced by many things. The parental investment may shed some light on the evolution of coloration in relation to female choice. In Oophaga pumilio, the female provides care for the offspring for several weeks whereas the males provides care for a few days, implying a strong female preference. Sexual selection increases phenotypic variation drastically. In populations of O. pumilio that participated in sexual selection, the phenotypic polymorphism was evident. The lack of sexual dimorphism in some dendrobatid populations however suggests that sexual selection is not a valid explanation.

Functional trade-offs are seen in poison frog defense mechanisms relating to toxin resistance. Poison dart frogs containing epibatidine have undergone a 3 amino acid mutation on receptors of the body, allowing the frog to be resistant to its own poison. Epibatidine-producing frogs have evolved poison resistance of body receptors independently three times. This target-site insensitivity to the potent toxin epibatidine on nicotinic acetylcholine receptors provides a toxin resistance while reducing the affinity of acetylcholine binding.

Captive care

Captive female D. auratus.

All species of poison dart frogs are Neotropical in origin. Wild-caught specimens can maintain toxicity for some time (this can be obtained through a form of bioaccumulation), so appropriate care should be taken when handling them. While scientific study on the lifespan of poison dart frogs is scant, retagging frequencies indicate it can range from one to three years in the wild. However, these frogs typically live for much longer than that in captivity, having been reported to live as long as 25 years. These claims also seem to be questionable, since many of the larger species take a year or more to mature, and Phyllobates species can take more than two years. In captivity, most species thrive where the humidity is kept constant at 80 to 100% and where the temperature is around 72 °F (22 °C) to 80 °F (27 °C) during the day and no lower than 60 °F (16 °C) to 65 °F (18 °C) at night. Some species tolerate lower temperatures better than others.

Conservation status

Many species of poison dart frogs have recently experienced habitat loss, chytrid diseases, and collection for the pet trade. Some are listed as threatened or endangered as a result. Zoos have tried to counteract this disease by treating captive frogs with an antifungal agent that is used to cure athlete's foot in humans.

Curare

From Wikipedia, the free encyclopedia

Chondrodendron tomentosum, main source plant of 'Tube Curare' and principal source of D-tubocurarine (DTC), the alkaloid constituting medicinal curare.
 
Strychnos toxifera, the Strychnos species which is the principal source of 'Calabash Curare' and its main active constituent - the alkaloid toxiferine

Curare (/kʊˈrɑːri/ or /kjʊˈrɑːri/; koo-rah-ree or kyoo-rah-ree) is a common name for various plant extract alkaloid arrow poisons originating from indigenous peoples in Central and South America. Used as a paralyzing agent for hunting and for therapeutic purposes, Curare only becomes active by a direct wound contamination by a poison dart or arrow or via injection. These poisons function by competitively and reversibly inhibiting the nicotinic acetylcholine receptor (nAChR), which is a subtype of acetylcholine receptor found at the neuromuscular junction. This causes weakness of the skeletal muscles and, when administered in a sufficient dose, eventual death by asphyxiation due to paralysis of the diaphragm. Curare is prepared by boiling the bark of one of the dozens of plant alkaloid sources, leaving a dark, heavy paste that can be applied to arrow or dart heads. Historically, curare has been used as an effective treatment for tetanus or strychnine poisoning and as a paralyzing agent for surgical procedures.

History

The word 'curare' is derived from wurari, from the Carib language of the Macusi of Guyana. It has its origins in the Carib phrase "mawa cure" meaning of the Mawa vine, scientifically known as Strychnos toxifera. Curare is also known among indigenous peoples as Ampi, Woorari, Woorara, Woorali, Wourali, Wouralia, Ourare, Ourari, Urare, Urari, and Uirary.

Classification

Initially, pharmacologist Rudolf Boehm's 1895 sought to classify the various alkaloid poisons based on the containers used for their preparation. During this investigation, he believed curare could be categorized into three main types as seen below . However useful it appeared, it became rapidly outmoded. Richard Gill, a plant collector, found that the indigenous peoples began to use a variety of containers for their curare preparations, henceforth invalidating Boehm's basis of classification.

  • Tube or bamboo curare: Mainly composed of the toxin D-tubocurarine, this poison is found packed into hollow bamboo tubes derived from Chondrodendron and other genera in the Menispermaceae. According to their LD50 values, tube curare is thought to be the most toxic.
  • Pot curare: Mainly composed of alkaloid components protocurarine (the active ingredient), protocurine (a weak toxicitiy), and protocuridine (non-toxic) from both Menispermaceae and Loganiaceae/Strychnaceae. This subtype is found originally packed in terra cotta pots.
  • calabash or gourd curare: Mainly composed of C toxiferine I, this poison is originally packed into hollow gourds from Loganiaceae/Strychnaceae alone.

Manske also observed in his 1955 The Alkaloids:

The results of the early [pre-1900] work were very inaccurate because of the complexity and variation of the composition of the mixtures of alkaloids involved ... these were impure, non-crystalline alkaloids ... Almost all curare preparations were and are complex mixtures, and many of the physiological actions attributed to the early curarizing preparations were undoubtedly due to impurities, particularly to other alkaloids present. The curare preparations are now considered to be of two main types, those from Chondrodendron or other members of the Menispermaceae family and those from Strychnos, a genus of the Loganiaceae [ now Strychnaceae ] family. Some preparations may contain alkaloids from both ... and the majority have other secondary ingredients.

Hunting uses

Curare was used as a paralyzing poison by many South American indigenous people. Since it was too expensive to be used in warfare, curare was mainly used during hunting. The prey was shot by arrows or blowgun darts dipped in curare, leading to asphyxiation owing to the inability of the victim's respiratory muscles to contract. In particular, the poison was used by the Island Caribs, indigenous people of the Lesser Antilles in the Caribbean, on the tips of their arrows. In addition, the Yagua people, indigenous to Colombia and northeastern Peru, commonly used these toxins in their blowpipes to target prey 30 to 40 paces distant.

Due to its popularity among the indigenous people as means of paralyzing prey, certain tribes would create monopolies from curare production. Thus, curare became a symbol of wealth among the indigenous populations.

In 1596, Sir Walter Raleigh mentioned the arrow poison in his book Discovery of the Large, Rich, and Beautiful Empire of Guiana (which relates to his travels in Trinidad and Guayana), though the poison he described possibly was not curare. In 1780, Abbe Felix Fontana discovered that it acted on the voluntary muscles rather than the nerves and the heart. In 1832, Alexander von Humboldt gave the first western account of how the toxin was prepared from plants by Orinoco River natives.

Curare darts and quiver from the Amazon rainforest.

During 1811–1812, Sir Benjamin Collins Brody experimented with curare (woorara). He was the first to show that curare does not kill the animal and the recovery is complete if the animal's respiration is maintained artificially. In 1825, Charles Waterton described a classical experiment in which he kept a curarized female donkey alive by artificial respiration with a bellows through a tracheostomy. Waterton is also credited with bringing curare to Europe. Robert Hermann Schomburgk, who was a trained botanist, identified the vine as one of the genus Strychnos and gave it the now accepted name Strychnos toxifera.

Medical use

George Harley (1829–1896) showed in 1850 that curare (wourali) was effective for the treatment of tetanus and strychnine poisoning. In 1857, Claude Bernard (1813–1878) published the results of his experiments in which he demonstrated that the mechanism of action of curare was a result of interference in the conduction of nerve impulses from the motor nerve to the skeletal muscle, and that this interference occurred at the neuromuscular junction. From 1887, the Burroughs Wellcome catalogue listed under its 'Tabloids' brand name, 112 grain (5.4 mg) tablets of curare (price: 8 shillings) for use in preparing a solution for hypodermic injection. In 1914, Henry Hallett Dale (1875–1968) described the physiological actions of acetylcholine. After 25 years, he showed that acetylcholine is responsible for neuromuscular transmission, which can be blocked by curare.

19th century depiction of hunting with blowguns in the Amazon rainforest.

The best known and historically most important (because of its medical applications) toxin is d-tubocurarine. It was isolated from the crude drug – from a museum sample of curare – in 1935 by Harold King of London, working in Sir Henry Dale's laboratory. King also established its chemical structure. Pascual Scannone, a Venezuelan anesthesiologist who trained and specialized in New York City, did extensive research on curare as a possible paralyzing agent for patients during surgical procedures. In 1942, he became the first person in all of Latin America to use curare during a medical procedure when he successfully performed a tracheal intubation in a patient to whom he administered curare for muscle paralysis at the El Algodonal Hospital in Caracas, Venezuela.

After its introduction in 1942, curare/curare-derivatives became a widely used paralyzing agent during medical and surgical procedures. In medicine, curare has been superseded by a number of curare-like agents, such as pancuronium, which have a similar pharmacodynamic profile, but fewer side effects.

Chemical structure

The various components of curare are organic compounds classified as either isoquinoline or indole alkaloids. Tubocurarine is one of the major active components in the South American dart poison. As an alkaloid, tubocurarine is a naturally occurring compound that consists of nitrogenous bases, although the chemical structure of alkaloids is highly variable.

Similar functional groups among the three compounds enables curare to bind to Acetylcholine receptors.

Like most alkaloids, tubocurarine and C toxiferine consist of a cyclic system with a nitrogen atom in an amine group. On the other hand, while acetylcholine does not contain a cyclic system, it does contain an amine group. Because of this amine group, curare alkaloids can bind readily to the active site of receptors for acetylcholine (ACh) at the neuromuscular junction, blocking nerve impulses from being sent to the skeletal muscles, effectively paralyzing the muscles of the body.

Pharmacological properties

A neuromuscular junction. Curare blocks Ach receptors (bottom left).

Curare is an example of a non-depolarizing muscle relaxant that blocks the nicotinic acetylcholine receptor (nAChR), one of the two types of acetylcholine (ACh) receptors, at the neuromuscular junction. The main toxin of curare, d-tubocurarine, occupies the same position on the receptor as ACh with an equal or greater affinity, and elicits no response, making it a competitive antagonist. The antidote for curare poisoning is an acetylcholinesterase (AChE) inhibitor (anti-cholinesterase), such as physostigmine or neostigmine. By blocking ACh degradation, AChE inhibitors raise the amount of ACh in the neuromuscular junction; the accumulated ACh will then correct for the effect of the curare by activating the receptors not blocked by toxin at a higher rate.

The time of onset varies from within one minute (for tubocurarine in intravenous administration, penetrating a larger vein), to between 15 and 25 minutes (for intramuscular administration, where the substance is applied in muscle tissue).

It is harmless if taken orally because curare compounds are too large and highly charged to pass through the lining of the digestive tract to be absorbed into the blood. For this reason, people can safely eat curare-poisoned prey, and it has no effect on its flavor.

Anesthesia

Isolated attempts to use curare during anesthesia date back to 1912 by Arthur Lawen of Leipzig, but curare came to anesthesia via psychiatry (electroplexy). In 1939 Abram Elting Bennett used it to modify metrazol induced convulsive therapy. Muscle relaxants are used in modern anesthesia for many reasons, such as providing optimal operating conditions and facilitating intubation of the trachea. Before muscle relaxants, anesthesiologists needed to use larger doses of the anesthetic agent, such as ether, chloroform or cyclopropane to achieve these aims. Such deep anesthesia risked killing patients who were elderly or had heart conditions.

The source of curare in the Amazon was first researched by Richard Evans Schultes in 1941. Since the 1930s, it was being used in hospitals as a muscle relaxant. He discovered that different types of curare called for as many as 15 ingredients, and in time helped to identify more than 70 species that produced the drug.

In the 1940s, it was used on a few occasions during surgery as it was mistakenly thought to be an analgesic or anesthetic. The patients reported feeling the full intensity of the pain though they were not able to do anything about it since they were essentially paralyzed.

On January 23, 1942, Harold Griffith and Enid Johnson gave a synthetic preparation of curare (Intercostrin/Intocostrin) to a patient undergoing an appendectomy (to supplement conventional anesthesia). Safer curare derivatives, such as rocuronium and pancuronium, have superseded d-tubocurarine for anesthesia during surgery. When used with halothane d-tubocurarine can cause a profound fall in blood pressure in some patients as both the drugs are ganglion blockers. However, it is safer to use d-tubocurarine with ether.

In 1954, an article was published by Beecher and Todd suggesting that the use of muscle relaxants (drugs similar to curare) increased death due to anesthesia nearly sixfold. This was refuted in 1956.

Modern anesthetists have at their disposal a variety of muscle relaxants for use in anesthesia. The ability to produce muscle relaxation irrespective of sedation has permitted anesthetists to adjust the two effects independently and on the fly to ensure that their patients are safely unconscious and sufficiently relaxed to permit surgery. The use of neuromuscular blocking drugs carries with it the risk of anesthesia awareness.

Plant sources

There are dozens of plants from which isoquinoline and indole alkaloids with curarizing effects can be isolated, and which were utilized by indigenous tribes of Central and South America for the production of arrow poisons. Among them are:

In family Menispermaceae:

Other families:

Some plants in the family Aristolochiaceae have also been reported as sources.

Alkaloids with curare-like activity are present in plants of the fabaceous genus Erythrina.

Toxicity

The toxicity of curare alkaloids in humans has not been established. Administration must be parenterally, as gastro-intestinal absorption is ineffective.

LD50 (mg/kg)

human: 0.735 est. (form and method of administration not indicated)

mouse: pot: 0.8–25; tubo: 5-10; calabash: 2–15.

Preparation

In 1807, Alexander von Humboldt provided the first eye-witness account of curare preparation. A mixture of young bark scrapings of the Strychnos plant, other cleaned plant parts, and occasionally snake venom is boiled in water for two days. This liquid is then strained and evaporated to create a dark, heavy, viscid paste that would be tested for its potency later. This curare paste was described to be very bitter in taste.

In 1938, Richard Gill and his expedition collected samples of processed curare and described its method of traditional preparation; one of the plant species used at that time was Chondrodendron tomentosum.

Adjuvants

Various irritating herbs, stinging insects, poisonous worms, and various parts of amphibians and reptiles are added to the preparation. Some of these accelerate the onset of action or increase the toxicity; others prevent the wound from healing or blood from coagulating.

Diagnosis and management of curare poisoning

Curare poisoning can be indicated by typical signs of neuromuscular-blocking drugs such as paralysis including respiration but not directly affecting the heart.

Curare poisoning can be managed by artificial respiration such as mouth-to-mouth resuscitation. In a study of 29 army volunteers that were paralyzed with curare, artificial respiration managed to keep an oxygen saturation of always above 85%, a level at which there is no evidence of altered state of consciousness. Yet, curare poisoning mimics the total locked-in syndrome in that there is paralysis of every voluntarily controlled muscle in the body (including the eyes), making it practically impossible for the victim to confirm consciousness while paralyzed.

Spontaneous breathing is resumed after the end of the duration of action of curare, which is generally between 30 minutes and 8 hours, depending on the variant of the toxin and dosage. Cardiac muscle is not directly affected by curare, but if more than four to six minutes has passed since respiratory cessation the cardiac muscle may stop functioning by oxygen-deprivation, making cardiopulmonary resuscitation including chest compressions necessary.

Chemical antidote

Since tubocurarine and the other components of curare bind reversibly to the ACh receptors, treatment for curare poisoning involves adding an acetylcholinesterase (AChE) inhibitor, which will stop the destruction of acetylcholine so that it can compete with curare. This can be done by administration of acetylcholinesterase (AChE) inhibitors such as pyridostigmine, neostigmine, physostigmine, and edrophonium. Acetylcholinesterase is an enzyme used to break down the acetylcholine (ACh) neurotransmitter left over in motor neuron synapses. The aforementioned inhibitors, termed "anticurare" drugs, reversibly bind to the enzyme's active site, prohibiting its ability to bind to its original target, ACh. By blocking ACh degradation, AChE inhibitors can effectively raise the amount of ACh present in the neuromuscular junction. The accumulated ACh will then correct for the effect of the curare by activating the receptors not blocked by toxin at a higher rate, restoring activity to the motor neurons and bodily movement.

Gallery

 

Blowgun

From Wikipedia, the free encyclopedia

Demonstration of a blowgun by a Yahua hunter

A blowgun (also called a blowpipe or blow tube) is a simple ranged weapon consisting of a long narrow tube for shooting light projectiles such as darts. It operates by having the projectile placed inside the pipe and using the force created by forced exhalation ("blow") to pneumatically propel the projectile. The propulsive power is limited by the strength of the user's respiratory muscles and the vital capacity of their lungs.

History

Many cultures have used such a weapon, but various indigenous peoples of Eastern Asia, Southeast Asia, Western Europe, North America, Central America (the Huehuetenango region of Guatemala), and South America (the Amazon Basin and the Guianas) are best known for its historical usage.

Projectiles include seeds, clay pellets, and darts. Some cultures dip the tip of the darts in curare or other arrow poisons in order to paralyze the target. Blowguns were very rarely used by these tribes as anti-personnel weapons, but primarily to hunt small animals such as monkeys and birds. North American Cherokees were known for making blowguns from river cane to supplement their diet with rabbits and other small creatures.

Blowguns are depicted in paintings on pre-Columbian pottery and are mentioned in many Mesoamerican myths. Back then and today, the Maya use a blowgun to hunt birds and small animals with spherical dry seeds and clay pellets. The clay ammunition is made slightly larger than needed (to allow for shrinkage and refinement) and stored in a shoulderbag. The outside of the dry clay pellet is shaved off and burnished right before use.

Shorter blowguns and smaller bore darts were used for varmint hunting by pre-adolescent boys in traditional Cherokee villages. They used the blowguns to cut down on small rodents such as rats, mice, chipmunks and other mammals that cut or gnaw into food caches, seed and vegetable stores, or that are attracted to the planted vegetables. While this custom gave the boys something to do around the village and kept them out of mischief, it also worked as an early form of pest control. Some food was also obtained by the boys, who hunted squirrels with blowguns well into the 20th century.

Today blowguns are used with tranquilizer darts to capture wildlife or to stun caged dangerous animals. Herpetologists use blowguns to capture elusive lizards with stun darts. Blowguns are also used recreationally, with either darts or paintballs.

Sport blowgun

There are several competition styles practised around the world. A standardization of competition style, based upon fukiya, is being pursued by the International Fukiyado Association and hopes to become an Olympic event. It is a 10-metre (33 ft) target shooting, using a standardized length 120 cm or 48 inch, and barrel caliber, dart shape, length and weight are free. In each round the shooter shoots 5 darts and there are 6 rounds per game, for a total of 30 darts. The target faces are 7 (6 cm), 5 (12 cm), 3 (18 cm) points. The bullseye is 160 cm above the floor.

Two other styles are also being pursued to make up the Olympic blowgun event, both based upon the Cherokee Annual Gathering Blowgun Competition. The Field Style competition is similar to the winter Biathlon, where the shooter runs from a starting line to a target lane, shoots and retrieves the darts, and continues to the next station. The course length varies from 400 to 800 m (440 to 870 yd) or longer, with from 9 to 16 targets at various heights and shooting distances. The final style is the Long Distance target shoot. The target is a circle of 24 cm (9 in) diameter, and the firing line is 20 m (66 ft) away. Three darts are fired by each shooter, at least one of which must stick in the target. All successful shooters move to the next round, moving back 2 m (6.6 ft) each time.

The sport blowgun competition is managed by the International Fukiyado Association, with which national associations in the United States, France, Germany and the Philippines are affiliated.

Gallery

Materials

Darts are typically made of hardwoods to prevent cracking, although bamboo skewers can be used informally. The dart's fletch can be made of many materials, such as down, feather tips, and animal fur. Modern materials, such as aluminium or carbon-reinforced plastic, are also used.

In Japan, the competition darts are made of cone shaped cellophane rolled into a cone (Fukiya), topped with a non-pointed brass brad. The Japan Sports Fukiya Association JSFA has privatized the sport, and all materials must be purchased from them. International Fukiya Association IFA chairman H.Higuchi promotes worldwide blowgun rule cooperating with other countries.

In other nations, the modified piano wire is used to make the 0.40 in (10 mm) cal and 0.50 in (13 mm) cal darts, with certain manufacturers making specialty darts for odd sized or larger caliber barrels (0.35 in [9 mm] cal, 0.625 in [16 mm] cal, 0.68 in [17 mm] cal, and 0.75 in [19 mm] cal).

Use of home-made darts in the larger sizes, or for hunting is common, utilizing bamboo skewers (3 and 6 mm or 18 and 14 in diameter), wire coat hangers, and even nails, or knitting needles.

Specifications

As a primitive weapon, there are no set dimension for a blowgun's length and diameter. However, generally there are several sizes:

  1. Fukidake — diameter is 13 mm (0.51 in) cal in Japan. Tournament length is 120 cm (47 in), but for practice one can use a 50 cm (20 in) tube. No mouthpiece is used; users wrap their lips around the tube. International versions can be slightly more flexible, allowing a tube of 122 cm (4 ft) and 13 mm (0.50 in) cal under IFA rules. Darts consist of a paper cone 20 cm (8 in) long, weighing 0.8 g (3100 oz).
  2. Cherokee – made of river cane, 2 to 3 m (6 to 9 ft). Dart is 15 to 56 cm (6 to 22 in) long and made of locustwood or other available hardwoods such as oak, ash, maple, walnut, etc., fletched with thistle down or rabbit fur, that provides an air seal.
  3. Jakaltek — wooden blowgun averages 1 m (3 ft) long with a sight placed 30 cm (12 in) from the end. Clay pellets are the most common type of ammunition and clay is sometimes added under the sight when the diameter of the blowgun is too thin for more stability and a better aim.
  4. Modern (US/EU) — typically has a diameter of 0.40 in (10 mm) cal, however, both the 0.50 in (13 mm) cal and 0.625 in (16 mm) cal are admitted for competitive shooting, with restrictions on barrel length and darts dimensions/weight; with varying lengths having distance restrictions imposed. Bell-shaped mouthpiece. Standard length limited to 121 cm (48 in) in IFA sanctioned competition.
  5. Paintball marker — made to be identical to the size of a 0.68 in (17 mm) cal paintball.
  6. Sumpit — usually about 1.2 to 1.8 m (4 to 6 ft) in length and 2 to 3 cm (0.79 to 1.18 in) in diameter. It is made from bamboo or wood, and can a single piece or two to three pieces joined together. Metal spearheads are uniquely commonly affixed at the tip, allowing them to also be used as stabbing weapons. They use thick short darts with soft cork plugs or resin-coated feathers or fibers at the blunt end. Bird-hunting versions can use clay pellets.

Legality

A law was passed in Guatemala in the 1930s outlawing the use of the blowgun in an effort to protect small game. It was difficult to enforce in rural areas, but was one of the reasons for the decline of blowgun use in Guatemala.

In the United Kingdom under the Criminal Justice Act 1988, and in Australia, the blowgun is categorized as an offensive weapon, and as such it is illegal to manufacture, sell or hire or offer for sale or hire, expose or have in one's possession for the purpose of sale or hire, or lend or give to any other person. Antique blowguns are, however, exempt.

In Canada, the blowgun is classified as a prohibited weapon and is defined as any device that "being a tube or pipe designed for the purpose of shooting arrows or darts by the breath". Any imported blowgun must be deactivated by either drilling a hole or by blocking it.

In the Republic of Ireland, blowpipes (blow guns) are classified as illegal offensive weapons.

In the US State of California, blowguns are illegal. They are also illegal in Massachusetts and the District of Columbia, but are legal elsewhere. There is currently no age requirement for using a blowgun.

Poisoned darts

Shooting darts with a blowgun is an extremely stealthy, and even lethal, hunting technique if the darts are poisoned with plant extracts or animal secretions. In Guyana, Suriname, French Guiana, some isolated areas in South America, and in the Amazon and Orinoco basins, blowgun hunters impregnate the tips of their darts with curare. The explorer Joseph Gumilla first mentioned the use of this poison. In ancient literature, it's also referred to as uiraêry, uirary, uraré, woorara, and wourali.

The Ticuas, an ethnic group from Brazil, Columbia, and Peru, produce a type of curare called Ticuna. This poison acts quickly on the prey, killing birds like the toucan in a matter of three to four minutes and small monkeys in about eight to ten minutes.

In the Orinoco basin, the blowgun and curare are used by: the Hoti, who make blowguns that are unique in their components; the Panare, who obtain blowguns from the Hoti; the Huottuja, or Piaroa, who get their blowguns from the Yekuana or Maquiritares; the Maquiritare, who get their curare from the Piaroa; and the Pemones, who also get their blowguns from the Yekuana or Maquiritares, though they make their own curare.

In the upper Rio Negro basin, the combination of blowguns and poisoned darts is used by the Curripacos, or Banivas, who make their own blowguns using technology and materials different, in part, from those of the ethnic groups of the Orinoco. They also produce their own curare. Their ancestors, the Waodani, used a match known as kakapa along with the curare to impregnate the darts of their blowpipes.

The Piaroa are known for making curare to impregnate the darts of their blowguns. They produce it beginning with extracts of different species of plants from the Strychnos genus - mainly maracure (Strychnos crevauxii)- mixed with kraraguero sap to increase the adhesion of the poison. An animal hit by a dart poisoned using the Piaroa recipe usually dies within fifteen minutes, depending on its body mass.

In the Philippines, Borneo, and Sulawesi, the sumpit (or sumpitan) blowgun darts are typically coated in the sap of Antiaris toxicaria (upas) which causes convulsions and death by cardiac arrest. Uniquely among blowguns, sumpit are also commonly tipped with metal spearheads for use in close combat or when the ammunition is exhausted, functionally similar to bayonets.

The Orang Asli of Peninsular Malaysia use the concentrated sap of Antiaris toxicaria (Malay : ipoh) to coat the point of their darts.

 

Genotype

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