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系统性美洲大蠊中毒,虽少见但更致命:磷脂酶 D 参与了美洲大蠊毒液的病理生理学过程。

Systemic Loxoscelism, Less Frequent but More Deadly: The Involvement of Phospholipases D in the Pathophysiology of Envenomation.

机构信息

Department of Cell Biology, Federal University of Paraná (UFPR), Curitiba 81531-980, Brazil.

Department of Structural, Molecular Biology and Genetics, State University of Ponta Grossa (UEPG), Ponta Grossa 84030-900, Brazil.

出版信息

Toxins (Basel). 2022 Dec 27;15(1):17. doi: 10.3390/toxins15010017.

Abstract

Bites of spiders can lead to a set of clinical manifestations called loxoscelism, and are considered a public health problem in many regions. The signs and symptoms of loxoscelism are divided into cutaneous and systemic forms. The former is more frequent and includes signs of envenoming at the bite site or neighboring regions. Systemic loxoscelism, although much less frequent, is associated with complications, and can even lead to death. It may include intravascular hemolysis, acute renal failure, and thrombocytopenia. venoms are enriched with phospholipases D (PLDs), which are a family of isoforms found at intra-species and inter-species levels. Under experimental conditions, these enzymes reproduce the main clinical signs of loxoscelism, including an exacerbated inflammatory response at the bite site and dermonecrosis, as well as thrombocytopenia, intravascular hemolysis, and acute renal failure. The role of PLDs in cutaneous loxoscelism was described over forty years ago, when studies identified and purified toxins featured as sphingomyelinase D. More recently, the production of recombinant PLDs and discoveries about their structure and mechanism has enabled a deeper characterization of these enzymes. In this review, we describe these biochemical and functional features of PLDs that determine their involvement in systemic loxoscelism.

摘要

蜘蛛咬伤可导致一系列临床症状,称为“游走性红斑症”,在许多地区被视为公共卫生问题。游走性红斑症的体征和症状分为皮肤型和系统型。前者更为常见,包括咬伤部位或邻近区域的中毒迹象。尽管系统型游走性红斑症不太常见,但与并发症相关,甚至可能导致死亡。它可能包括血管内溶血、急性肾衰竭和血小板减少症。

毒液富含磷脂酶 D(PLD),这是一种在种内和种间水平都存在的同工酶家族。在实验条件下,这些酶可复制游走性红斑症的主要临床症状,包括咬伤部位炎症反应加剧和皮肤坏死,以及血小板减少症、血管内溶血和急性肾衰竭。PLD 在皮肤游走性红斑症中的作用早在四十多年前就已被描述,当时的研究鉴定并纯化了具有神经鞘磷脂酶 D 特征的毒素。最近,重组 PLD 的生产以及对其结构和机制的发现,使这些酶得到了更深入的特征描述。在这篇综述中,我们描述了决定其参与系统性游走性红斑症的这些生化和功能特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac57/9864854/058cc39e5005/toxins-15-00017-g001.jpg

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