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缓激肽B2受体拮抗剂可减少脱氧胆酸钠诱导的搔抓行为。

Reduction of sodium deoxycholic acid-induced scratching behaviour by bradykinin B2 receptor antagonists.

作者信息

Hayashi I, Majima M

机构信息

Department of Pharmacology, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan. hayashii@med. kitasato-u.ac.jp

出版信息

Br J Pharmacol. 1999 Jan;126(1):197-204. doi: 10.1038/sj.bjp.0702296.

Abstract
  1. Subcutaneous injection of sodium deoxycholic acid into the anterior of the back of male ddY mice elicited dose-dependent scratching of the injected site with the forepaws and hindpaws. 2. Up to 100 microg of sodium deoxycholic acid induced no significant increase in vascular permeability at the injection site as assessed by a dye leakage method. 3. Bradykinin (BK) B2 receptor antagonists, FR173657 and Hoe140, significantly decreased the frequency of scratching induced by sodium deoxycholic acid. 4. Treatment with aprotinin to inhibit tissue kallikrein reduced the scratching behaviour induced by sodium deoxycholic acid, whereas treatment with soybean trypsin inhibitor to inhibit plasma kallikrein did not. 5. Although injection of kininase II inhibitor, lisinopril together with sodium deoxycholic acid did not alter the scratching behaviour, phosphoramidon, a neutral endopeptidase inhibitor, significantly increased the frequency of scratching. 6. Homogenates of the skin excised from the backs of mice were subjected to gel-filtration column chromatography followed by an assay of kinin release by trypsin from each fraction separated. Less kinin release from the fractions containing kininogen of low molecular weight was observed in the skin injected with sodium deoxycholic acid than in normal skin. 7. The frequency of scratching after the injection of sodium deoxycholic acid in plasma kininogen-deficient Brown Norway Katholiek rats was significantly lower than that in normal rats of the same strain, Brown Norway Kitasato rats. 8. These results indicate that BK released from low-molecular-weight kininogen by tissue kallikrein, but not from high-molecular-weight kininogen by plasma kallikrein, may be involved in the scratching behaviour induced by the injection of sodium deoxycholic acid in the rodent.
摘要
  1. 向雄性ddY小鼠背部前方皮下注射脱氧胆酸钠,可引起前爪和后爪对注射部位的剂量依赖性抓挠。2. 通过染料渗漏法评估,注射部位注射高达100微克脱氧胆酸钠未引起血管通透性显著增加。3. 缓激肽(BK)B2受体拮抗剂FR173657和Hoe140显著降低了脱氧胆酸钠诱导的抓挠频率。4. 用抑肽酶抑制组织激肽释放酶可减少脱氧胆酸钠诱导的抓挠行为,而用大豆胰蛋白酶抑制剂抑制血浆激肽释放酶则无此作用。5. 尽管注射激肽酶II抑制剂赖诺普利与脱氧胆酸钠一起并未改变抓挠行为,但中性内肽酶抑制剂磷酰胺素显著增加了抓挠频率。6. 从小鼠背部切除的皮肤匀浆经凝胶过滤柱层析,然后对每个分离组分用胰蛋白酶进行激肽释放测定。与正常皮肤相比,注射脱氧胆酸钠的皮肤中,含低分子量激肽原的组分激肽释放较少。7. 在血浆激肽原缺陷的棕色挪威Katholiek大鼠中,注射脱氧胆酸钠后的抓挠频率显著低于同一品系的正常大鼠棕色挪威北里大鼠。8. 这些结果表明,由组织激肽释放酶从低分子量激肽原释放的BK,而非由血浆激肽释放酶从高分子量激肽原释放的BK,可能参与了啮齿动物注射脱氧胆酸钠诱导的抓挠行为。

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