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α-硫辛酸对线粒体超氧阴离子和糖皮质激素诱导的高血压的影响。

The effect of alpha-lipoic acid on mitochondrial superoxide and glucocorticoid-induced hypertension.

机构信息

Department of Renal Medicine, St George Hospital, Kogarah, NSW 2217, Australia.

出版信息

Oxid Med Cell Longev. 2013;2013:517045. doi: 10.1155/2013/517045. Epub 2013 Feb 26.

Abstract

AIMS

To examine the effect of alpha-lipoic acid, an antioxidant with mitochondrial superoxide inhibitory properties, on adrenocorticotrophic hormone- (ACTH-HT) and dexamethasone-induced hypertensions (DEX-HT) in rats and if any antihypertensive effect is mediated via mitochondrial superoxide inhibition.

METHODS

In a prevention study, rats received ground food or alpha-lipoic-acid-laced food (10 mg/rat/day) for 15 nights. Saline, adrenocorticotrophic hormone (ACTH, 0.2 mg/kg/day), or dexamethasone (DEX, 10  μ g/rat/day) was injected subcutaneously from day 5 to day 11. In a reversal study, rats received alpha-lipoic-acid-laced food 4 days after commencement of saline or DEX. Tail-cuff systolic blood pressure (SBP) was measured second daily. Kidney mitochondrial superoxide was examined using (MitoSOX) Red (MitoSOX) via flow cytometry.

RESULTS

SBP was increased by ACTH (P < 0.0005) and DEX (P < 0.0005). Alpha-lipoic acid alone did not alter SBP. With alpha-lipoic acid pretreatment, SBP was increased by ACTH (P' < 0.005) but not by DEX. Alpha-lipoic partially prevented ACTH-HT (P' < 0.0005) and fully prevented DEX-HT (P' < 0.0005) but failed to reverse DEX-HT. ACTH and DEX did not increase MitoSOX signal. In ACTH-hypertensive rats, high-dose alpha-lipoic acid (100 mg/rat/day) did not decrease SBP further but raised MitoSOX signal (P < 0.001), suggesting prooxidant activity.

CONCLUSION

Glucocorticoid-induced hypertension in rats is prevented by alpha-lipoic acid via mechanisms other than mitochondrial superoxide reduction.

摘要

目的

研究抗氧化剂α-硫辛酸(具有抑制线粒体超氧化物的特性)对促肾上腺皮质激素-(ACTH-HT)和地塞米松诱导的高血压(DEX-HT)的影响,以及任何降压作用是否通过抑制线粒体超氧化物来介导。

方法

在预防研究中,大鼠连续 15 晚接受普通食物或含α-硫辛酸的食物(10mg/大鼠/天)喂养。从第 5 天到第 11 天,每天皮下注射盐水、促肾上腺皮质激素(ACTH,0.2mg/kg/天)或地塞米松(DEX,10μg/大鼠/天)。在逆转研究中,大鼠在开始接受盐水或 DEX 后的第 4 天开始接受含α-硫辛酸的食物。每天测量两次尾套收缩压(SBP)。通过流式细胞术使用(MitoSOX)Red(MitoSOX)检测肾线粒体中超氧化物。

结果

ACTH(P < 0.0005)和 DEX(P < 0.0005)均可使 SBP 升高。单独使用α-硫辛酸不会改变 SBP。用α-硫辛酸预处理,ACTH 可使 SBP 升高(P' < 0.005),但 DEX 则不能。α-硫辛酸部分预防 ACTH-HT(P' < 0.0005)并完全预防 DEX-HT(P' < 0.0005),但不能逆转 DEX-HT。ACTH 和 DEX 均未增加 MitoSOX 信号。在 ACTH 高血压大鼠中,高剂量α-硫辛酸(100mg/大鼠/天)不会进一步降低 SBP,但会增加 MitoSOX 信号(P < 0.001),提示具有促氧化剂活性。

结论

α-硫辛酸通过除减少线粒体超氧化物以外的机制预防大鼠的糖皮质激素诱导性高血压。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15d2/3600316/502459380dba/OXIMED2013-517045.001.jpg

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