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镉暴露通过内皮细胞氧化应激诱导血管损伤:局部血管紧张素 II 和 COX-2 的作用。

Cadmium exposure induces vascular injury due to endothelial oxidative stress: the role of local angiotensin II and COX-2.

机构信息

Departamento de Ciências Fisiológicas, Universidade Federal do Espírito Santo, 29040-091 Vitória, ES, Brazil.

Departamento de Ciências Fisiológicas, Universidade Federal do Espírito Santo, 29040-091 Vitória, ES, Brazil.

出版信息

Free Radic Biol Med. 2013 Dec;65:838-848. doi: 10.1016/j.freeradbiomed.2013.08.167. Epub 2013 Aug 22.

Abstract

Cadmium is an environmental pollutant that is closely linked with cardiovascular diseases, such as atherosclerosis and hypertension. Moreover, cadmium can induce an increase in oxidative stress. One of the main sites affected by oxidative stress is the aorta, which consequently develops atherosclerosis. However, there are few reports demonstrating aortic effects induced by small concentrations of cadmium that are similar to those found in the blood resulting from occupational exposure. Furthermore, several studies have reported on chronic cadmium exposure, and the results of these studies may have been influenced by the secondary effects induced by this metal, such as hypertension. Therefore, we investigated the effects of acute cadmium exposure on the vascular reactivity to phenylephrine of aortic rings isolated from male Wistar rats. Cadmium increased phenylephrine reactivity without changing the vasorelaxation induced by acetylcholine and sodium nitroprusside. Endothelial damage or incubation with L-NAME shifted the phenylephrine concentration-response curves leftward in arteries incubated with or without cadmium, but the curves were shifted to a lesser degree after cadmium incubation. Enalapril, losartan, the nonselective COX inhibitor indomethacin, the TXA(2) synthase inhibitor furegrelate, the selective COX-2 inhibitor NS 398, the TP receptor antagonist SQ 29.548, the EP1 receptor antagonist SC 19.220, superoxide dismutase, and the NADPH oxidase inhibitor apocynin partially reverted the cadmium-induced effects on the reactivity to phenylephrine. Cadmium exposure increased vasoconstrictor activity by reducing NO bioavailability owing to the increased production of ROS by NADPH oxidase. The results of the tested cadmium concentration, which is below the reference values, suggest that acute cadmium exposure may induce vascular injury through endothelial oxidative stress. These data contribute to the evidence indicating that cadmium is a high risk to public health.

摘要

镉是一种环境污染物,与心血管疾病密切相关,如动脉粥样硬化和高血压。此外,镉可诱导氧化应激增加。氧化应激的主要部位之一是主动脉,因此会发展为动脉粥样硬化。然而,很少有报道表明小浓度的镉对主动脉的影响类似于职业暴露导致血液中的镉浓度。此外,一些研究报告了慢性镉暴露,这些研究的结果可能受到该金属诱导的继发性影响的影响,例如高血压。因此,我们研究了急性镉暴露对雄性 Wistar 大鼠主动脉环对苯肾上腺素血管反应性的影响。镉增加了苯肾上腺素的反应性,而不改变乙酰胆碱和硝普钠诱导的血管舒张。内皮损伤或用 L-NAME 孵育将苯肾上腺素浓度-反应曲线向左移位,在孵育有或没有镉的动脉中,但在镉孵育后曲线向左移位的程度较小。依那普利、氯沙坦、非选择性 COX 抑制剂吲哚美辛、TXA(2)合酶抑制剂 furegrelate、选择性 COX-2 抑制剂 NS 398、TP 受体拮抗剂 SQ 29.548、EP1 受体拮抗剂 SC 19.220、超氧化物歧化酶和 NADPH 氧化酶抑制剂 apocynin 部分逆转了镉对苯肾上腺素反应性的影响。镉暴露通过增加 NADPH 氧化酶产生的 ROS 来降低 NO 的生物利用度,从而增加血管收缩活性。测试的镉浓度低于参考值,这表明急性镉暴露可能通过内皮氧化应激引起血管损伤。这些数据有助于表明镉对公众健康构成高风险的证据。

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