Extraordinary variance in meta-analysis of venom toxicity of 160 most lethal ophidians and guidelines for estimating human lethal dose range.

Journal of biological methods Pub Date : 2024-10-24 eCollection Date: 2024-01-01 DOI:10.14440/jbm.2024.0037
Brian P Hanley, Gustavo Gross
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引用次数: 0

Abstract

Background: This is the first meta-analysis to characterize intra-ophidian-species variation in whole venom. Being the largest possible meta-analysis at this time, it encompasses all known records of animal lethality studies over the past 100 years. These results were not artifacts of resistant test-animal species and showed orders of magnitude beyond the 1.6 logs (40-fold change) range of lethal dose documented in the literature between amphibians, lizards, and mice.

Methods: A total of 1003 lethal dose study results for 160 of the most lethal venomous ophidian species in the world were analyzed.

Results: LDLo was not different from LD50 across studies, indicating the true range of toxicity is probably larger. The belief that, for the route of inoculation, IC < IV < IP < IM < SC was well supported (R2 = 0.90). However, 5% of ICs were the highest dose, and 7% of SC inoculations were the lowest dose. Within the mouse test species, for one route of inoculation, the widest LD range was 2.96 logs (917-fold change, N = 20). Within mouse species, for multiple routes of inoculation, the widest LD range was 3.6 logs (4,150-fold change, N = 20). The strongest correlation for the range of lethal dose results was the number of studies (R2 = 0.56), followed by the number of test-animal species (R2 = 0.55) and then the number of routes of inoculation (R2 = 0.43).

Conclusion: Scientists working with humans should use combined LDLo and LD50 meta-datasets for all data and calculate mean, median, minimum, range, and standard deviation as shown in the supplement spreadsheet, and the equations we provide. Standard deviation multiples may provide the desired safety for experimenters. For estimating the LD50 range and minimum lethal dose for species with little data, we recommend curating a meta-dataset of related snakes, and computational research to strengthen this estimation.

对 160 种最致命的蚜虫毒液毒性进行荟萃分析时发现的巨大差异以及估算人类致死剂量范围的准则。
背景:这是首次对嗜食性动物全毒液的种内变异进行荟萃分析。作为目前规模最大的荟萃分析,它涵盖了过去 100 年中所有已知的动物致死率研究记录。这些结果并非抗性试验动物物种的伪影,其数量级超出了两栖类、蜥蜴和小鼠之间文献记载的 1.6 logs(40 倍变化)致死剂量范围:方法:分析了世界上最致命的 160 种毒蛇的 1003 项致死剂量研究结果:结果:各项研究的 LDLo 与 LD50 并无差异,这表明毒性的真实范围可能更大。在接种途径方面,IC < IV < IP < IM < SC 这一观点得到了很好的支持(R2 = 0.90)。然而,5%的IC接种是最高剂量,7%的SC接种是最低剂量。在小鼠试验物种中,对于一种接种途径,最宽的 LD 范围为 2.96 logs(917 倍变化,N = 20)。在小鼠试验物种中,对于多种接种途径,最宽 LD 范围为 3.6 logs(4,150 倍变化,N = 20)。与致死剂量结果范围相关性最强的是研究数量(R2 = 0.56),其次是试验动物物种数量(R2 = 0.55),然后是接种途径数量(R2 = 0.43):从事人类研究的科学家应使用 LDLo 和 LD50 元数据集来计算所有数据,并计算平均值、中位数、最小值、范围和标准偏差,如补充电子表格和我们提供的公式所示。标准偏差倍数可为实验者提供所需的安全性。对于估计数据较少的物种的半数致死剂量范围和最小致死剂量,我们建议整理相关蛇类的元数据集,并通过计算研究来加强这种估计。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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