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2型糖尿病患者血液中L-精氨酸依赖性一氧化氮的产生:一项为期五年的前瞻性试点研究。

L-Arginine-Dependent Nitric Oxide Production in the Blood of Patients with Type 2 Diabetes: A Pilot, Five-Year Prospective Study.

作者信息

Stoian Irina, Iosif Liviu, Gilca Marilena, Vlad Adelina, Tivig Ioan, Bradescu Ovidiu Marius, Savu Octavian

机构信息

Department of Functional Sciences I/Biochemistry, Faculty of Medicine, Carol Davila University of Medicine and Pharmacy, 050474 Bucharest, Romania.

IristLabmed SRL, 031235 Bucharest, Romania.

出版信息

Life (Basel). 2024 Apr 26;14(5):556. doi: 10.3390/life14050556.

Abstract

: Type 2 diabetes mellitus (T2DM) is a major cardiovascular risk factor. Nitric oxide (NO) is one of the many molecules that regulate vascular tone, and red blood cells (RBCs) are known to play an important role in adjusting cardiac function through NO export from RBCs. Our study prospectively investigated the L-arginine (L-arg)-nitric oxide (NO) metabolic pathway in the erythrocytes and plasma of subjects with T2DM. RBCs and plasma were collected from patients with T2DM (n = 10), at first clinical onset (baseline) and after five years of disease evolution (follow-up). L-arg content was assayed by competitive enzyme-linked immunoassay. Arginase activity and nitrate/nitrite levels were measured using spectrophotometry. : When compared to baseline, L-arg content decreased in RBCs and remained similar in the plasma; NO production decreased in RBCs and the plasma; and arginase activity was lower in RBCs and increased in plasma. : The L-arg/NO metabolic pathway decreases in the RBCs of patients with T2DM five years after the first clinical onset. The persistent decrease in RBCs' arginase activity fails to compensate for the sustained decrease in RBCs' NO production in the diabetic environment. This pilot study indicates that the NO-RBC pool is depleted during the progression of the disease in the same cohort of T2DM patients.

摘要

2型糖尿病(T2DM)是主要的心血管危险因素。一氧化氮(NO)是众多调节血管张力的分子之一,已知红细胞(RBCs)通过红细胞输出NO在调节心脏功能中发挥重要作用。我们的研究前瞻性地调查了T2DM患者红细胞和血浆中的L-精氨酸(L-arg)-一氧化氮(NO)代谢途径。从T2DM患者(n = 10)中收集红细胞和血浆,在首次临床发病时(基线)和疾病进展五年后(随访)。通过竞争性酶联免疫测定法测定L-arg含量。使用分光光度法测量精氨酸酶活性和硝酸盐/亚硝酸盐水平。与基线相比,红细胞中L-arg含量降低,血浆中保持相似;红细胞和血浆中NO生成减少;红细胞中精氨酸酶活性降低,血浆中增加。首次临床发病五年后,T2DM患者红细胞中的L-arg/NO代谢途径降低。在糖尿病环境中,红细胞精氨酸酶活性持续降低无法补偿红细胞NO生成的持续减少。这项初步研究表明,在同一队列的T2DM患者疾病进展过程中,NO-红细胞池会耗尽。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecf6/11122261/0c70c24d490e/life-14-00556-g001.jpg

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