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P物质和辣椒素对链脲佐菌素诱导的糖尿病大鼠胃底和回肠的影响。

Effect of substance P and capsaicin on stomach fundus and ileum of streptozotocin-diabetic rats.

作者信息

Pinna C, Bolego C, Puglisi L

机构信息

Institute of Pharmacological Sciences, University of Milan, Italy.

出版信息

Eur J Pharmacol. 1995 Mar 24;276(1-2):61-9. doi: 10.1016/0014-2999(95)00004-5.

Abstract

The in vitro responses of longitudinal preparations of rat stomach fundus and ileum to capsaicin at 1, 8, 4, 16 and 26 weeks and to substance P at 1 and 8 weeks from diabetes induction were studied. The results were compared with those obtained in age-matched control rats. The contractile responses to exogenous substance P and capsaicin were not affected in the stomach fundus from diabetic rats. Atropine (1 microM) did not antagonize the substance P-induced response whereas it inhibited about 90% of the capsaicin-induced response in controls and about 60% of the response in diabetic rats. At the resting tone, capsaicin induced a relaxation followed by a contraction in stomach fundus of control rats. Only a contraction was evoked in diabetic rats. In carbachol (0.05-0.1 microM) pre-stimulated strips, a complete restoration of the biphasic response was obtained in the diabetic state. The contractile response elicited by exogenous substance P was not significantly increased in the ileum preparations from diabetic rats; nevertheless the EC50 value for substance P was reduced 8 weeks after the onset of diabetes. The response elicited by capsaicin in the ileum of control rats was also biphasic. The capsaicin-induced contraction was greater in tissue from diabetic rats as compared with controls and relaxation was not evident. An age-related decrease of the contraction was also evident in both groups. Atropine (1 microM) partially antagonized the responses to substance P and capsaicin. The inhibition of the responses with atropine was more evident in control than in diabetic rats. These results suggest that the myogenic actions of several agonists in these two tissues are differently modified in experimental diabetes.

摘要

研究了糖尿病诱导后1、8、4、16和26周时大鼠胃底和回肠纵向制剂对辣椒素以及1和8周时对P物质的体外反应。将结果与年龄匹配的对照大鼠所得结果进行比较。糖尿病大鼠胃底对外源性P物质和辣椒素的收缩反应未受影响。阿托品(1微摩尔)不能拮抗P物质诱导的反应,而在对照中它抑制约90%的辣椒素诱导的反应,在糖尿病大鼠中抑制约60%的反应。在静息张力下,辣椒素在对照大鼠胃底诱导先松弛后收缩。在糖尿病大鼠中仅诱发收缩。在卡巴胆碱(0.05 - 0.1微摩尔)预刺激的条带上,糖尿病状态下双相反应完全恢复。糖尿病大鼠回肠制剂中外源性P物质引发的收缩反应未显著增加;然而糖尿病发病8周后P物质的半数有效浓度(EC50)值降低。辣椒素在对照大鼠回肠中引发的反应也是双相的。与对照相比,糖尿病大鼠组织中辣椒素诱导的收缩更大,且松弛不明显。两组中与年龄相关的收缩减少也很明显。阿托品(1微摩尔)部分拮抗对P物质和辣椒素的反应。阿托品对反应的抑制在对照中比在糖尿病大鼠中更明显。这些结果表明,在实验性糖尿病中,这两种组织中几种激动剂的肌源性作用有不同程度的改变。

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