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一氧化氮,一种1,4 - 二氢吡啶诱导血管平滑肌光舒张的可能介质。

Nitric oxide, a possible mediator of 1,4-dihydropyridine-induced photorelaxation of vascular smooth muscle.

作者信息

Lovren F, O'Neill S K, Bieger D, Igbal N, Knaus E E, Triggle C R

机构信息

Smooth Muscle Research Group, Faculty of Medicine, University of Calgary, Alberta, Canada.

出版信息

Br J Pharmacol. 1996 Jun;118(4):879-84. doi: 10.1111/j.1476-5381.1996.tb15481.x.

Abstract
  1. In rat aortic tissues pre-contracted with phenylephrine, certain 1,4-dihydropyridines (DHPs) such as Bay K 8644 (0.1 microM), PN 202791 (1 microM), RK 30 (1 microM), NI 104 (1 microM) and NI 105 (1 microM) enhanced photoactivated relaxations (photorelaxation or PR) whereas NI 72, NI 85, NI 99, NI 102, amlodipine, felodipine, nifedipine and nimodipine were inactive. 2. The PR inducing effects of Bay K 8644 were mimicked by the diabetogenic agent, streptozotocin (STZ). 3. Solutions of Bay K 8644 which had been irradiated for various periods of time initiated light independent transient relaxations followed by contractile responses in aortic tissue partially contracted with phenylephrine. With exposure times to light of 30 to 120 min, the intensity of the relaxation response to irradiated Bay K 8644 increased from 26 +/- 3.3 to 71 +/- 3.7% of the maximum contractile response to phenylephrine (n = 5). Conversely the contractile responses decreased, from 84.2 +/- 4.1 to 19.8 +/- 10.4% of the maximum contractile response to phenylephrine (n = 5). 4. Superoxide ions, generated by incubation of xanthine (2mM) plus xanthine oxidase (10 mu ml-1) in physiological saline solution (PSS) NaCl 118, KCl 4.7, CaCl2 2.5, KH2PO4 1.2, MgSO4 1.2, NaHCO3 12.5 and glucose 11.1 (mM) for 1 h. reduced the PR induced by DHPs, STZ, and also NO-induced relaxations of rat aortic preparations. 5. Direct measurements of NO indicate that, following exposure to a polychromatic light source, equimolar concentrations (0.1 mM) of the DHP compounds that enhance PR, as well as STZ, photodegrade to release NO (25 +/- 2-40.3 +/- 5.9 nmol min-1, n = 6). 6. Structure-activity studies indicate that a nitro group at the -3 position of the dihydropyridine ring is essential for DHPs to support PR. 7. These data suggest that the photodegradation of DHPs and STZ leading to the release of NO provides the primary cellular process underlying the PR response.
摘要
  1. 在用去氧肾上腺素预收缩的大鼠主动脉组织中,某些1,4 - 二氢吡啶类化合物(DHPs),如Bay K 8644(0.1微摩尔)、PN 202791(1微摩尔)、RK 30(1微摩尔)、NI 104(1微摩尔)和NI 105(1微摩尔)可增强光激活舒张(光舒张或PR),而NI 72、NI 85、NI 99、NI 102、氨氯地平、非洛地平、硝苯地平和尼莫地平则无活性。2. 致糖尿病药物链脲佐菌素(STZ)可模拟Bay K 8644的PR诱导作用。3. 经不同时间照射的Bay K 8644溶液可引发与光无关的短暂舒张,随后在用去氧肾上腺素部分收缩的主动脉组织中出现收缩反应。光照30至120分钟后,照射后的Bay K 8644舒张反应强度从去氧肾上腺素最大收缩反应的26±3.3%增加至71±3.7%(n = 5)。相反,收缩反应从去氧肾上腺素最大收缩反应的84.2±4.1%降至19.8±10.4%(n = 5)。4. 通过在生理盐溶液(PSS,NaCl 118、KCl 4.7、CaCl2 2.5、KH2PO4 1.2、MgSO4 1.2、NaHCO3 12.5和葡萄糖11.1(毫摩尔))中孵育黄嘌呤(2毫摩尔)加黄嘌呤氧化酶(10微升/毫升)1小时产生的超氧阴离子,可降低DHPs、STZ诱导的PR以及大鼠主动脉制剂中NO诱导的舒张。5. NO的直接测量表明,在暴露于多色光源后,增强PR的DHP化合物以及STZ的等摩尔浓度(0.1毫摩尔)会发生光降解以释放NO(25±2 - 40.3±5.9纳摩尔/分钟,n = 6)。6. 构效关系研究表明,二氢吡啶环 - 3位的硝基对于DHPs支持PR至关重要。7. 这些数据表明,DHPs和STZ的光降解导致NO释放是PR反应的主要细胞过程。

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