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Investigation on inhibition of biological effects of endothelin

机译:抑制内皮素生物学作用的研究

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The effects of a series of substances on the biological function of endothelin (ET) are reported. The substances used are: synthetic inhibitors of endothelium derived relaxing factors (EDRFs), inhibitor of big-endothelin converting enzyme phosphoramidon, antiserum of endothelin, antagonists of endothelin A receptor BQ123 and JKC301, and two Chinese anti-snake venom herb medicines Lobelia radicans Thumb and Tarts polyphylla Smith var. chinensis (Franch) Hara. The results showed that inhibiting the production of nitric oxide (NO) could stimulate ET release from vascular endothelium, elevate plasma ET and increase blood pressure. These changes could be reversed by L-arginine (L-Arg), the substrate of nitric oxide synthase (NOS). The amount of ET released by arterial endothelium could be increased or inhibited by inhibiting or stimulating the synthesis of prostacyclin (PGI_2). The plasma ET level and blood pressure in both SHR and WKY rats could be decreased by giving phosphoramidon (PhR). The above results indicate that the biological effects of ET could be" antagonized by inhibiting the synthesis or release of ET, decreasing the level of plasma ET, blocking the binding of ET with its receptor and using some Chinese anti-snake venom herb medicines.
机译:据报道一系列物质对内皮素(ET)的生物学功能的影响。使用的物质包括:内皮衍生松弛因子(EDRF)的合成抑制剂,大内皮素转化酶磷酰胺的抑制剂,内皮素的抗血清,内皮素A受体BQ123和JKC301的拮抗剂,以及两种中毒蛇毒中草药Lobelia radicans Thumb和Tar叶史密斯变种。中华(原)哈拉。结果表明,抑制一氧化氮(NO)的产生可以刺激ET从血管内皮中释放,升高血浆ET并增加血压。一氧化氮合酶(NOS)的底物L-精氨酸(L-Arg)可以逆转这些变化。通过抑制或刺激前列环素(PGI_2)的合成,可以增加或抑制动脉内皮释放的ET量。给予磷酰胺(PhR)可以降低SHR和WKY大鼠的血浆ET水平和血压。以上结果表明,通过抑制ET的合成或释放,降低血浆ET的水平,阻断ET与受体的结合以及使用一些中国的抗蛇毒草药,可以拮抗ET的生物学作用。

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