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眼镜蛇蛇毒致局部坏死的发病机制:评估台湾产冻干神经毒素抗蛇毒血清在动物模型中的中和能力。

Pathogenesis of local necrosis induced by Naja atra venom: Assessment of the neutralization ability of Taiwanese freeze-dried neurotoxic antivenom in animal models.

机构信息

Molecular Medicine Research Center, Chang Gung University, Taoyuan, Taiwan.

Department of Emergency Medicine, En Chu Kong Hospital, New Taipei City, Taiwan.

出版信息

PLoS Negl Trop Dis. 2020 Feb 7;14(2):e0008054. doi: 10.1371/journal.pntd.0008054. eCollection 2020 Feb.

Abstract

Naja atra envenomation is one of the most significant clinical snakebite concerns in Taiwan. Taiwanese freeze-dried neurotoxic antivenom (FNAV) is currently used clinically for the treatment of cobra snakebite, and has been shown to limit the mortality of cobra envenomation to less than 1%. However, more than half of victims (60%) require surgery because of local tissue necrosis, a major problem in patients with cobra envenomation. Although the importance of evaluating the neutralizing effect of FNAV on this pathology is recognized, whether FNAV is able to prevent the local necrosis extension induced by N. atra venom has not been investigated in detail. Cytotoxins (CTXs) are considered as the major components of N. atra venom that cause necrosis. In the current study, we isolated CTXs from whole cobra venom and used both whole venom and purified CTXs to develop animal models for assessing the neutralization potential of FNAV against venom necrotizing activity. Local necrotic lesions were successfully produced in mice using CTXs in place of whole N. atra venom. FNAV was able to rescue mice from a subcutaneously injected lethal dose of cobra venom; however, it was unable to prevent CTX-induced dermo-necrosis. Furthermore, using the minimal necrosis dose (MND) of CTXs and venom proteome data, we found a dose of whole N. atra venom suitable for FNAV and developed a workable protocol for inducing local necrosis in rodent models that successfully imitated the clinical circumstance of cobra envenoming. This information provides a more comprehensive understanding of the pathophysiology of N. atra envenomation, and serves as a guide for improving current antivenom strategies and advancing clinical snakebite management in Taiwan.

摘要

中华眼镜蛇咬伤是台湾地区最受关注的蛇伤临床问题之一。目前,临床使用的台湾产冻干神经毒素抗蛇毒血清(FNAV)治疗眼镜蛇咬伤,已证实可将眼镜蛇咬伤的死亡率降低至 1%以下。然而,超过一半的(60%)患者需要手术治疗,原因是局部组织坏死,这是眼镜蛇咬伤患者的一个主要问题。尽管人们认识到评估 FNAV 对这种病理的中和作用的重要性,但尚未详细研究 FNAV 是否能够防止眼镜蛇毒液引起的局部坏死扩展。细胞毒素(CTXs)被认为是引起坏死的眼镜蛇毒液的主要成分。在本研究中,我们从全蛇毒中分离出 CTXs,并使用全蛇毒和纯化的 CTXs 开发动物模型,以评估 FNAV 对毒液坏死活性的中和潜力。使用 CTXs 代替全眼镜蛇毒液成功地在小鼠中产生了局部坏死病变。FNAV 能够挽救皮下注射致死剂量眼镜蛇毒液的小鼠,但不能防止 CTX 诱导的真皮坏死。此外,使用 CTXs 的最小坏死剂量(MND)和毒液蛋白质组数据,我们找到了适合 FNAV 的全眼镜蛇毒液剂量,并开发了一种可行的方案,可在啮齿动物模型中诱导局部坏死,成功模拟了眼镜蛇咬伤的临床情况。这些信息提供了对眼镜蛇咬伤病理生理学的更全面了解,并为改进当前抗蛇毒血清策略和推进台湾地区临床蛇伤管理提供了指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ff4/7032728/4895b809a5a8/pntd.0008054.g001.jpg

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