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组胺通过激活大鼠体内心脏的胞外5'-核苷酸酶来增加间质腺苷浓度。

Histamine increases interstitial adenosine concentration via activation of ecto-5'-nucleotidase in rat hearts in vivo.

作者信息

Obata T, Kubota S, Yamanaka Y

机构信息

Department of Pharmacology, Oita Medical University, Hasama-machi, Oita, Japan.

出版信息

J Pharmacol Exp Ther. 2001 Jul;298(1):71-6.

Abstract

We examined whether histamine enhances the production of interstitial adenosine via stimulation of ecto-5'-nucleotidase (a key enzyme responsible for adenosine production) using microdialysis techniques in in situ rat hearts. The microdialysis probe was implanted in the left ventricular myocardium of anesthetized rats and perfused in the presence of adenosine 5'-monophosphate (AMP). Histamine (10-500 microM) administered into the perfusate had a tendency to increase the adenosine concentration. In the presence of prazosin (50 microM), an antagonist of alpha1-adrenoceptors, or of chelerythrine (10 microM), a protein kinase C (PKC) inhibitor, and in reserpinized rats, histamine failed to increase the AMP-primed dialysate adenosine concentration. Accumulation of norepinephrine in the extracellular fluid elicited by pargyline (100 microM), a monoamine oxidase inhibitor, significantly increased histamine-induced adenosine production. Okadaic acid (50 microM), an inhibitor of protein phosphatase, enhanced the histamine-induced increase in adenosine concentration. Norepinephrine is known to activate alpha1-adrenoceptors and PKC. Taken together, the results demonstrate that histamine-released norepinephrine activates both alpha1-adrenoceptors and PKC, which increased ecto-5'-nucleotidase activity and augmented release of adenosine in rat hearts.

摘要

我们使用微透析技术在大鼠原位心脏中研究了组胺是否通过刺激胞外5'-核苷酸酶(一种负责腺苷生成的关键酶)来增强间质腺苷的生成。将微透析探针植入麻醉大鼠的左心室心肌,并在存在5'-单磷酸腺苷(AMP)的情况下进行灌注。向灌注液中加入组胺(10 - 500微摩尔)有增加腺苷浓度的趋势。在存在α1-肾上腺素能受体拮抗剂哌唑嗪(50微摩尔)或蛋白激酶C(PKC)抑制剂白屈菜红碱(10微摩尔)的情况下,以及在利血平化的大鼠中,组胺未能增加AMP引发的透析液腺苷浓度。单胺氧化酶抑制剂帕吉林(100微摩尔)引起的细胞外液中去甲肾上腺素的积累显著增加了组胺诱导的腺苷生成。蛋白磷酸酶抑制剂冈田酸(50微摩尔)增强了组胺诱导的腺苷浓度增加。已知去甲肾上腺素可激活α1-肾上腺素能受体和PKC。综上所述,结果表明组胺释放的去甲肾上腺素激活了α1-肾上腺素能受体和PKC,从而增加了大鼠心脏中胞外5'-核苷酸酶的活性并增强了腺苷的释放。

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