Sarangi B, Kar P K, Datta A, Gomes A, Lahiri S C
Department of Pharmacology, School of Tropical Medicine, Calcutta, India.
Indian J Exp Biol. 1990 Jun;28(6):557-61.
The venom of V. cincta contains acetylcholine (ACh), histamine and 5-hydroxytryptamine (5-HT). Blockers of these agonists did not block completely the hypotensive and smooth muscle contractile activity of venom. On smooth muscle, there was a residual slow contraction. The active substance which produced this slow contraction was separated by solvent extraction, gel filtration and TLC. The purified material (which has been provisionally designated "Vecikinin") lowered cat, rat and guinea pig blood pressure, increased amplitude of cardiac contraction, and increased capillary permeability. Vecikinin contracted several smooth muscle preparations (rat uterus, rat ascending colon, guinea pig ileum, guinea pig colon and rat ileum), while relaxing rat duodenum. Its contractile activity was not lost on boiling, but acid or alkali-boiling reduced its contractile activity. It was inactivated on incubation with chymotrypsin and carboxypeptidase but not with trypsin, pepsin or leucine aminopeptidase. It is a peptide, appears to be of low molecular weight, and could be distinguished from substance P, angiotensin, bradykinin and hornet or wasp kinin.
环带蝰蛇的毒液含有乙酰胆碱(ACh)、组胺和5-羟色胺(5-HT)。这些激动剂的阻滞剂并不能完全阻断毒液的降压和平滑肌收缩活性。在平滑肌上,存在残余的缓慢收缩。通过溶剂萃取、凝胶过滤和薄层层析分离出产生这种缓慢收缩的活性物质。纯化后的物质(暂命名为“Vecikinin”)可降低猫、大鼠和豚鼠的血压,增加心脏收缩幅度,并增加毛细血管通透性。Vecikinin可使多种平滑肌制剂(大鼠子宫、大鼠升结肠、豚鼠回肠、豚鼠结肠和大鼠回肠)收缩,同时使大鼠十二指肠松弛。其收缩活性在煮沸时不会丧失,但经酸或碱煮沸会降低其收缩活性。与胰凝乳蛋白酶和羧肽酶孵育时会使其失活,但与胰蛋白酶、胃蛋白酶或亮氨酸氨肽酶孵育时则不会。它是一种肽,似乎分子量较低,且可与P物质、血管紧张素、缓激肽以及黄蜂或胡蜂激肽区分开来。