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高同型半胱氨酸血症对大鼠海绵体中α1-肾上腺素能受体介导的收缩的影响:活性氧的作用。

Consequence of hyperhomocysteinaemia on α1-adrenoceptor-mediated contraction in the rat corpus cavernosum: the role of reactive oxygen species.

作者信息

Côco Hariane, Pernomian Larissa, Marchi Katia C, Gomes Mayara S, de Andrade Cláudia R, Ramalho Leandra N Z, Tirapelli Carlos R, de Oliveira Ana M

机构信息

Departament of Pharmacology, Faculdade de Medicina de Ribeirão Preto, Ribeirão Preto, SP, Brazil.

Laboratory of Vascular Injury, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Ribeirão Preto, SP, Brazil.

出版信息

J Pharm Pharmacol. 2016 Jan;68(1):63-75. doi: 10.1111/jphp.12486. Epub 2016 Jan 4.

Abstract

OBJECTIVES

Our main objective was to investigate the mechanisms underlying the effects of hyperhomocysteinaemia (HHcy) on contractile response mediated by α1-adrenoceptors in the rat corpus cavernosum.

METHODS

Concentration-response curves for phenylephrine (PE) were obtained in strips of corpus cavernosum, in absence or after incubation with tiron, tempol or polyethylene glycol (PEG)-catalase combined or not with tempol. We also measured the superoxide anion (O2(-)) and hydrogen peroxide (H2O2) generation, superoxide dismutase (SOD) and catalase activity and α-actin expression in rat corpus cavernosum from both groups.

KEY FINDINGS

HHcy increased PE-induced contraction in cavernosal strips. Tiron, PEG-catalase or tempol increased PE-induced contraction in strips from control rats, but it was not altered by tiron or PEG-catalase in HHcy rats, whereas tempol reduced this response. The combination of PEG-catalase and tempol did not alter the contractile response to PE in both groups. HHcy increased O2(-) generation and SOD activity, whereas H2O2 concentration was reduced. Finally, HHcy did not alter catalase activity or expression of α-actin.

CONCLUSIONS

The major new finding from this study is that HHcy induced a marked increase in PE-induced contraction in rat corpus cavernosum by a mechanism that involves increased O2(-) generation and it could play a role in the pathogenesis of erectile dysfunction associated with HHcy.

摘要

目的

我们的主要目的是研究高同型半胱氨酸血症(HHcy)对大鼠海绵体中由α1 -肾上腺素能受体介导的收缩反应产生影响的潜在机制。

方法

在海绵体条带中获取去氧肾上腺素(PE)的浓度 - 反应曲线,分别在未处理或用铁螯合剂、Tempol或聚乙二醇(PEG) - 过氧化氢酶孵育后(单独或与Tempol联合使用)进行测量。我们还测量了两组大鼠海绵体中超氧阴离子(O2(-))和过氧化氢(H2O2)的生成、超氧化物歧化酶(SOD)和过氧化氢酶活性以及α -肌动蛋白表达。

主要发现

HHcy增加了海绵体条带中PE诱导的收缩。铁螯合剂、PEG - 过氧化氢酶或Tempol增加了对照大鼠海绵体条带中PE诱导的收缩,但在HHcy大鼠中,铁螯合剂或PEG - 过氧化氢酶对其无改变,而Tempol降低了这种反应。PEG - 过氧化氢酶和Tempol的组合在两组中均未改变对PE的收缩反应。HHcy增加了O2(-)的生成和SOD活性,而H2O2浓度降低。最后,HHcy未改变过氧化氢酶活性或α -肌动蛋白的表达。

结论

本研究的主要新发现是,HHcy通过涉及增加O2(-)生成的机制,诱导大鼠海绵体中PE诱导的收缩显著增加,并且它可能在与HHcy相关的勃起功能障碍的发病机制中起作用。

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