Antiarin
Antiarins are cardiac glycoside poisons produced by the upas tree. There are two closely related forms, α-antiarin and β-antiarin. The two share the same aglycone, antiarigenin, but differ in the sugar group that is attached to it.
α-Antiarin
α-Antiarin is a crystalline solid with a melting point of 242-242.5 °C. The sugar portion of α-antiarin is antiarose.In addition to being present in the sap of the upas tree, it is also found in the latex of Naucleopsis mello-barretoi.
β-Antiarin
Is a crystalline solid with a melting point of 233-240 °C. The sugar portion of β-antiarin is L-rhamnose.The uses of β-antiarin range from medical use, such as hypertension treatment, to arrow poison application. It also proves to be more poisonous than curare, sporting a low of 0.1 mg/kg in most mammals.
Symptoms of β-antiarin poisoning
Upon β-antiarin poisoning, when observed in animals such as frogs and small mammals, visible symptoms include muscle spasms — particularly of the head and neck — and excess defecation. Paralysis can also be presented before death. The primary physiological system affected is the cardiac muscle, though gastro-intestinal tissue has also been known to be severely affected by this type of poisoning. Convulsions and spasms are not immediate, especially when the chemical is too diluted in water. In animal tests, time of death resulted anywhere from 5–30 minutes after administration.When used as an arrow poison, β-antiarin produces twitches in the target, which then become full convulsions, unconsciousness, and final death through cardiac arrest.
Toxicity of β-antiarin
During tests performed on frogs and mammals, it was found that the minimum lethal dose for an amphibian was 1/300th mg. For a 300-400 g guinea pig, this lethal dose increased to 0.75 mg. Lethal dose for felines is 0.094 mg/kg, using intravenous injection. Meanwhile, 1 mg will kill a dog.Physiological systems affected/medical properties
β-Antiarin is administered to the body through injection. Once inside the body, the chemical will affect muscular and cardiac tissues. A heart attack occurs because β-antiarin affects Na+K+-ATPase cardiac-muscle membrane activity.However, the very effect that allows β-antiarin to be a poison also gives it medicinal properties. It limits the sodium ion concentration by blocking the pump, which then promotes calcium ions to increase in concentration in the extracellular cardiac muscle domain, therein permitting the heart to contract. The mechanism through which sodium and calcium ions are exchanged, known as the sodium-calcium exchanger, allows for the exchange of ions to occur at a rate of 3:1 respectively. The cardiac cell exhibits a positive potential during ventricular systole, becomes depolarized, and permits calcium ions to rush in by the NCX. From here, the contraction occurs when the calcium ions leave and the cell re-polarizes. If the dosage of cardiac glycoside doubles, then the substance becomes a poison.