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激肽B1受体的血管作用机制及用于研究这些受体的细胞模型的建立。

Vascular mode of action of kinin B1 receptors and development of a cellular model for the investigation of these receptors.

作者信息

Levesque L, Drapeau G, Grose J H, Rioux F, Marceau F

机构信息

Centre de recherche (Université Laval), Hôtel-Dieu de Québec, Canada.

出版信息

Br J Pharmacol. 1993 Aug;109(4):1254-62. doi: 10.1111/j.1476-5381.1993.tb13757.x.

Abstract
  1. Kinins exert a contractile effect on rabbit aortic rings via the stimulation of B1 receptors. Des-Arg9-bradykinin (BK) is more potent than BK on this receptor type. The mode of action of des-Arg9-BK on rabbit aortic tissue has been studied by both the aortic ring contractility assay and a cellular model using cultured aortic smooth muscle cells (SMCs). 2. The des-Arg9-BK-induced contractions in rabbit aortic rings were unaffected by pretreatments with nifedipine, indomethacin, REV-5901 (a 5-lipoxygenase blocker) and LY-83583 (a guanylyl cyclase inhibitor); however, the protein kinase inhibitors H-7 and H-9 significantly reduced the maximal effect of des-Arg9-BK. 3. The contractile responses to des-Arg9-BK in calcium-free Krebs solution were slightly but not significantly attenuated in amplitude, as compared to paired control tissues bathed in Krebs solution, and sustained plateaus of contraction were observed in the absence of Ca2+. However, Ca2+ replenishment further increased the kinin-induced contraction measured in Ca(2+)-free bathing fluid. 4. Despite the lack of evidence of a mediating role for prostaglandin in the mechanical response to des-Arg9-BK, the kinin stimulated the release of prostacyclin from rabbit aorta rings measured as immunoreactive 6-keto-prostaglandin F1 alpha (6-keto-PGF1 alpha). 5. Smooth muscle cells (SMCs) derived from the rabbit aorta exhibit functional responses to des-Arg9-BK in acute release of 6-keto-PGF1alpha and of inositol phosphate turnover which were inhibited by pretreatment with the B1 receptor antagonist, Lys[Leu8]des-Arg9-BK, but not by the B2 receptor antagonist, Hoe-140. Preincubation of the cells with interleukin- 1 (IL-1) 20 h before stimulation with the kinin had no effect on basal inositol phosphate turnover, but potentiated the acute effect of des-Arg9-BK.6. These results suggest that second mesengers derived from the action of phospholipase C are produced by SMCs when B1 receptors are activated in rabbit aortic tissue. Intracellular calcium stores are primarily mobilized by des-Arg9-BK, although receptor-controlled calcium influx has not been ruled out, and may contribute to initiate the contractile responses. The maintenance of the contractile state involves protein kinase C activity and is consistent with a current model of SMC function. The cell model retains some of the cardinal properties of B1 receptor-mediated vascular responses: endothelium independent PGI2 release and up-regulation by the cytokine IL-1. PGI2 is not involved in the mechanical response, possible because the rabbit aorta is refractory to this prostaglandin.
摘要
  1. 激肽通过刺激B1受体对兔主动脉环产生收缩作用。去-精氨酸9-缓激肽(BK)对该受体类型的作用比BK更强。已通过主动脉环收缩性测定和使用培养的主动脉平滑肌细胞(SMC)的细胞模型研究了去-精氨酸9-BK对兔主动脉组织的作用方式。2. 硝苯地平、吲哚美辛、REV-5901(一种5-脂氧合酶阻滞剂)和LY-83583(一种鸟苷酸环化酶抑制剂)预处理对去-精氨酸9-BK诱导的兔主动脉环收缩无影响;然而,蛋白激酶抑制剂H-7和H-9显著降低了去-精氨酸9-BK的最大效应。3. 与浸泡在Krebs溶液中的配对对照组织相比,在无钙Krebs溶液中对去-精氨酸9-BK的收缩反应幅度略有但不显著减弱,并且在无Ca2+时观察到持续的收缩平台期。然而,补充Ca2+进一步增加了在无Ca(2+)的浴液中测量的激肽诱导的收缩。4. 尽管缺乏前列腺素在对去-精氨酸9-BK的机械反应中起介导作用的证据,但该激肽刺激兔主动脉环释放前列环素,以免疫反应性6-酮-前列腺素F1α(6-酮-PGF1α)来衡量。5. 从兔主动脉衍生的平滑肌细胞(SMC)对去-精氨酸9-BK在急性释放6-酮-PGF1α和肌醇磷酸周转率方面表现出功能反应,这些反应被B1受体拮抗剂Lys[Leu8]去-精氨酸9-BK预处理所抑制,但不被B2受体拮抗剂Hoe-140所抑制。在用激肽刺激前20小时用白细胞介素-1(IL-1)预孵育细胞对基础肌醇磷酸周转率无影响,但增强了去-精氨酸9-BK的急性效应。6. 这些结果表明,当兔主动脉组织中的B1受体被激活时,平滑肌细胞产生源自磷脂酶C作用的第二信使。细胞内钙库主要由去-精氨酸9-BK动员,尽管尚未排除受体控制的钙内流,并且可能有助于启动收缩反应。收缩状态的维持涉及蛋白激酶C活性,并且与平滑肌细胞功能的当前模型一致。该细胞模型保留了B1受体介导的血管反应的一些基本特性:内皮依赖性前列环素释放和细胞因子IL-1的上调。前列环素不参与机械反应,可能是因为兔主动脉对这种前列腺素不敏感。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25dd/2175773/614f72449c97/brjpharm00721-0370-a.jpg

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