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碳酸酐酶、其抑制剂与血管功能。

Carbonic anhydrase, its inhibitors and vascular function.

作者信息

García-Llorca Andrea, Carta Fabrizio, Supuran Claudiu T, Eysteinsson Thor

机构信息

Department of Physiology, Faculty of Medicine, University of Iceland, Reykjavik, Iceland.

NEUROFARBA Department, Section of Pharmaceutical and Nutraceutical Sciences, University of Florence, Florence, Italy.

出版信息

Front Mol Biosci. 2024 Jan 29;11:1338528. doi: 10.3389/fmolb.2024.1338528. eCollection 2024.

Abstract

It has been known for some time that Carbonic Anhydrase (CA, EC 4.2.1.1) plays a complex role in vascular function, and in the regulation of vascular tone. Clinically employed CA inhibitors (CAIs) are used primarily to lower intraocular pressure in glaucoma, and also to affect retinal blood flow and oxygen saturation. CAIs have been shown to dilate vessels and increase blood flow in both the cerebral and ocular vasculature. Similar effects of CAIs on vascular function have been observed in the liver, brain and kidney, while vessels in abdominal muscle and the stomach are unaffected. Most of the studies on the vascular effects of CAIs have been focused on the cerebral and ocular vasculatures, and in particular the retinal vasculature, where vasodilation of its vessels, after intravenous infusion of sulfonamide-based CAIs can be easily observed and measured from the fundus of the eye. The mechanism by which CAIs exert their effects on the vasculature is still unclear, but the classic sulfonamide-based inhibitors have been found to directly dilate isolated vessel segments when applied to the extracellular fluid. Modification of the structure of CAI compounds affects their efficacy and potency as vasodilators. CAIs of the coumarin type, which generally are less effective in inhibiting the catalytically dominant isoform hCA II and unable to accept NO, have comparable vasodilatory effects as the primary sulfonamides on pre-contracted retinal arteriolar vessel segments, providing insights into which CA isoforms are involved. Alterations of the lipophilicity of CAI compounds affect their potency as vasodilators, and CAIs that are membrane impermeant do not act as vasodilators of isolated vessel segments. Experiments with CAIs, that shed light on the role of CA in the regulation of vascular tone of vessels, will be discussed in this review. The role of CA in vascular function will be discussed, with specific emphasis on findings with the effects of CA inhibitors (CAI).

摘要

一段时间以来,人们已经知道碳酸酐酶(CA,EC 4.2.1.1)在血管功能以及血管张力调节中发挥着复杂作用。临床使用的碳酸酐酶抑制剂(CAIs)主要用于降低青光眼患者的眼压,同时也会影响视网膜血流和血氧饱和度。已经证明,CAIs可使脑血管和眼血管扩张并增加血流量。在肝脏、脑和肾脏中也观察到了CAIs对血管功能的类似作用,而腹肌和胃部的血管则不受影响。大多数关于CAIs血管效应的研究都集中在脑血管和眼血管,尤其是视网膜血管,静脉输注基于磺胺类的CAIs后,其血管的血管舒张情况可以很容易地从眼底观察和测量到。CAIs对血管系统发挥作用的机制仍不清楚,但已发现经典的基于磺胺类的抑制剂在应用于细胞外液时可直接使分离的血管段扩张。CAI化合物结构的改变会影响其作为血管舒张剂的功效和效力。香豆素类的CAIs通常在抑制催化活性占主导的同工型hCA II方面效果较差,且无法接受NO,但在预收缩的视网膜小动脉血管段上具有与主要磺胺类药物相当的血管舒张作用,这为了解哪些CA同工型参与其中提供了线索。CAI化合物亲脂性的改变会影响其作为血管舒张剂的效力,而不能透过细胞膜的CAIs不会对分离的血管段起到血管舒张作用。本文将讨论有关CAIs的实验,这些实验揭示了CA在血管张力调节中的作用。我们将讨论CA在血管功能中的作用,特别强调CA抑制剂(CAI)作用的研究结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f988/10859760/686f68d015e2/fmolb-11-1338528-g001.jpg

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