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茶碱通过前列腺素途径使大鼠膈肌小动脉扩张。

Theophylline dilates rat diaphragm arterioles via the prostaglandins pathway.

作者信息

Danialou G, Vicaut E, Aubier M, Boczkowski J

机构信息

INSERM U408, Faculté Xavier Bichat, Paris, France.

出版信息

Br J Pharmacol. 1998 Aug;124(7):1355-62. doi: 10.1038/sj.bjp.0701962.

Abstract
  1. We investigated by intravital microscopy in rats, the in vivo direct effects of theophylline on the diameters of second and third order diaphragm arterioles. 2. Theophylline (1-100 microM) dilated second and third order diaphragm arterioles significantly, and with an amplitude which was not statistically different from the one obtained with adenosine (1-100 microM). Enprofylline (1-100 microM), a theophylline analogue with poor adenosine-receptor antagonism but with similar or higher phosphodiesterases inhibition properties than theophylline, also dilated diaphragm arterioles, causing however, a significantly smaller dilatation than theophylline. 3. Neither the A1 adenosine receptor antagonist 8-cyclopentyl-1,3-dipropylxanthine (CPX, 50 nM), nor the A2 adenosine receptor antagonist 3,7-dimethyl-1-proparglyxanthine (DMPX, 10 microM) reduced significantly theophylline-induced arteriolar dilatation. 4. Theophylline (100 nM) abolished adenosine-induced arteriolar dilatation. 5. The dilatation induced by theophylline was unchanged by the nitric oxide (NO) synthase inhibitor N(omega)-nitro-L-arginine (NNA, 300 microM). 6. Theophylline-induced arteriolar dilatation was abolished by the prostaglandin synthesis inhibitors mefenamic acid or indomethacin (20 microM). 7. These findings show that theophylline induced a significant dilatation of diaphragm arterioles via the release of prostaglandins.
摘要
  1. 我们通过对大鼠进行活体显微镜检查,研究了茶碱对第二和第三级膈肌小动脉直径的体内直接作用。2. 茶碱(1 - 100微摩尔)能显著扩张第二和第三级膈肌小动脉,其扩张幅度与腺苷(1 - 100微摩尔)所产生的幅度在统计学上无差异。恩丙茶碱(1 - 100微摩尔)是一种腺苷受体拮抗作用较弱但磷酸二酯酶抑制特性与茶碱相似或更高的茶碱类似物,它也能扩张膈肌小动脉,但其扩张程度明显小于茶碱。3. A1腺苷受体拮抗剂8 - 环戊基 - 1,3 - 二丙基黄嘌呤(CPX,50纳摩尔)和A2腺苷受体拮抗剂3,7 - 二甲基 - 1 - 丙炔基黄嘌呤(DMPX,10微摩尔)均未显著降低茶碱诱导的小动脉扩张。4. 茶碱(100纳摩尔)可消除腺苷诱导的小动脉扩张。5. 一氧化氮(NO)合酶抑制剂N(ω) - 硝基 - L - 精氨酸(NNA,300微摩尔)对茶碱诱导的扩张无影响。6. 前列腺素合成抑制剂甲芬那酸或吲哚美辛(20微摩尔)可消除茶碱诱导的小动脉扩张。7. 这些发现表明,茶碱通过释放前列腺素诱导膈肌小动脉显著扩张。

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