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腺苷刺激血管平滑肌细胞中一氧化氮的合成。

Adenosine stimulates nitric oxide synthesis in vascular smooth muscle cells.

作者信息

Ikeda U, Kurosaki K, Ohya K, Shimada K

机构信息

Department of Cardiology, Jichi Medical School, Tochigi, Japan.

出版信息

Cardiovasc Res. 1997 Jul;35(1):168-74. doi: 10.1016/s0008-6363(97)00068-0.

DOI:10.1016/s0008-6363(97)00068-0
PMID:9302361
Abstract

OBJECTIVE

The aim was to investigate the effects of adenosine on nitric oxide (NO) synthesis in vascular smooth muscle cells.

METHODS

NO and cAMP synthesis was measured in confluent rat vascular smooth muscle cells in culture at passage 5-10, using Griess reagent and an enzyme immunoassay kit, respectively. The expression of inducible NO synthase mRNA was assayed by Northern blotting.

RESULTS

Incubation of cultures with interleukin-1 beta (10 ng/ml) for 24 h caused a significant increase in nitrite production. The interleukin-1 beta-induced nitrite production by vascular smooth muscle cells was significantly increased by adenosine or its stable analogue, 2-chloroadenosine, in a dose-dependent manner. The adenosine A2a receptor antagonist, KF17837, but not the A1 receptor antagonist, DPCPX, significantly inhibited 2-chloroadenosine-mediated nitrite production. The 2-chloroadenosine-mediated nitrite production by interleukin-1 beta-stimulated cells was accompanied by increased inducible NO synthase mRNA accumulation. In the presence of dibutyryl-cAMP (1 mM), interleukin-1 beta-induced nitrite accumulation was further increased, but the effect of 2-chloroadenosine was not additive or synergistic. Addition of 2-chloroadenosine dose-dependently increased intracellular cAMP levels of vascular smooth muscle cells.

CONCLUSIONS

These results indicate that adenosine acts on A2 receptors and augments NO synthesis in interleukin-1 beta-stimulated vascular smooth muscle cells, at least partially through a cAMP-dependent pathway.

摘要

目的

研究腺苷对血管平滑肌细胞中一氧化氮(NO)合成的影响。

方法

分别使用格里斯试剂和酶免疫分析试剂盒,测定第5 - 10代培养的汇合大鼠血管平滑肌细胞中NO和环磷酸腺苷(cAMP)的合成。通过Northern印迹法检测诱导型一氧化氮合酶mRNA的表达。

结果

用白细胞介素 - 1β(10 ng/ml)孵育培养物24小时导致亚硝酸盐生成显著增加。腺苷或其稳定类似物2 - 氯腺苷以剂量依赖性方式显著增加血管平滑肌细胞由白细胞介素 - 1β诱导的亚硝酸盐生成。腺苷A2a受体拮抗剂KF17837可显著抑制2 - 氯腺苷介导的亚硝酸盐生成,而A1受体拮抗剂DPCPX则无此作用。白细胞介素 - 1β刺激的细胞中2 - 氯腺苷介导的亚硝酸盐生成伴随着诱导型一氧化氮合酶mRNA积累增加。在存在二丁酰 - cAMP(1 mM)的情况下,白细胞介素 - 1β诱导的亚硝酸盐积累进一步增加,但2 - 氯腺苷的作用无相加或协同效应。添加2 - 氯腺苷可剂量依赖性增加血管平滑肌细胞的细胞内cAMP水平。

结论

这些结果表明,腺苷作用于A2受体,至少部分通过cAMP依赖性途径增强白细胞介素 - 1β刺激的血管平滑肌细胞中的NO合成。

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