Primor N, Teitelbaum Z, Zlotkin E
Biochim Biophys Acta. 1980 Jan 3;627(1):71-81. doi: 10.1016/0304-4165(80)90124-5.
The oral toxicity of a radioiodinated toxic polypeptide isolated from a cobra snake venom as assayed by Sarcophaga falculata blowflies coupled with assays on competitive displacement have indicated that: (a) During 3--4 h 8% of the orally active toxin is able to pass through the digestive system of the fly; (b) the orally active toxin after passing the gut binds to body tissues. The strong affinity of the toxin to tissue membranes explains its absence in the insect's hemolymph following oral applications as well as injection. The removal of traces of phospholipase A, which is extremely toxic, by injection of the orally active toxin has significantly lowered its injection toxicity without affecting its oral toxicity, thus indicating the absence of any interaction with phospholipases in oral toxicity. This conclusion was supported by additional experimentation.
通过用厩螫蝇测定从眼镜蛇蛇毒中分离出的一种放射性碘化有毒多肽的口服毒性,并结合竞争性置换试验表明:(a) 在3 - 4小时内,8%的口服活性毒素能够穿过苍蝇的消化系统;(b) 口服活性毒素通过肠道后会与身体组织结合。毒素对组织膜的强亲和力解释了口服应用以及注射后昆虫血淋巴中没有毒素的原因。通过注射口服活性毒素去除剧毒的微量磷脂酶A,显著降低了其注射毒性,而不影响其口服毒性,因此表明在口服毒性中不存在与磷脂酶的任何相互作用。这一结论得到了进一步实验的支持。