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Kunitz-Type Peptides of the Sea Anemone Heteractis crispa: Potential Anti-Inflammatory Compounds

机译:海葵异相脆饼蛋白胨蛋白蛋白蛋白酶蛋白酶蛋白酶:潜在的抗炎化合物

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摘要

Antihistamine activity of recombinant peptides, Kunitz- type serine protease inhibitors of the sea anemone Heteractis crispa, was studied. It was shown that the peptides rHCGS1.19 and rHCGS1.36 at a concentration 10 mu Minhibit an increase in the calcium ion concentration in macrophages elicited by histamine at 62.2 and 84.0%, respectively. The anti-inflammatory effect can be seen as the result of mediated reactions between peptides and proteases involved in these processes, as with the histamine H-1-type receptor blocking.
机译:研究了重组肽的抗组胺药活性,研究了海葵异相抑制剂的Kunitz型丝氨酸蛋白酶抑制剂。 结果表明,肽Rhcgs1.19和rhcgs1.36的浓度10μmm,浓度在62.2和84.0%的组胺中引起的巨噬细胞中的钙离子浓度的增加。 作为这些方法所涉及的肽和蛋白酶之间的介导反应的结果,可以看到抗炎作用,与组胺H-1型受体阻断一样。

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    Russian Acad Sci GB Elyakov Pacific Inst Bioorgan Chem Far Eastern Branch Pr 100 Let Vladivostoku 159 Vladivostok 690022 Russia;

    Russian Acad Sci GB Elyakov Pacific Inst Bioorgan Chem Far Eastern Branch Pr 100 Let Vladivostoku 159 Vladivostok 690022 Russia;

    Russian Acad Sci GB Elyakov Pacific Inst Bioorgan Chem Far Eastern Branch Pr 100 Let Vladivostoku 159 Vladivostok 690022 Russia;

    Russian Acad Sci GB Elyakov Pacific Inst Bioorgan Chem Far Eastern Branch Pr 100 Let Vladivostoku 159 Vladivostok 690022 Russia;

    Russian Acad Sci GB Elyakov Pacific Inst Bioorgan Chem Far Eastern Branch Pr 100 Let Vladivostoku 159 Vladivostok 690022 Russia;

    Russian Acad Sci GB Elyakov Pacific Inst Bioorgan Chem Far Eastern Branch Pr 100 Let Vladivostoku 159 Vladivostok 690022 Russia;

    Russian Acad Sci GB Elyakov Pacific Inst Bioorgan Chem Far Eastern Branch Pr 100 Let Vladivostoku 159 Vladivostok 690022 Russia;

    Russian Acad Sci GB Elyakov Pacific Inst Bioorgan Chem Far Eastern Branch Pr 100 Let Vladivostoku 159 Vladivostok 690022 Russia;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

    sea anemone; Kunitz-type protease inhibitors; antihistamine activity;

    机译:海葵;Kunitz型蛋白酶抑制剂;抗组胺药活性;

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