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Involvement of prostaglandins in histamine H-1 receptor-operated Ca2+ entry in human gingival fibroblasts

机译:前列腺素参与人牙龈成纤维细胞中由组胺H-1受体操纵的Ca2 +进入

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摘要

In the absence of external Ca2+, 100 mu M histamine evoked a transient increase in intracellular Ca2+ ([Ca2+](i)), and subsequent addition of Ca2+ to the medium resulted in a sustained increase in [Ca2+](i) in fura-2-loaded human gingival fibroblasts. These Ca2+ mobilizations are attributed to Ca2+ release from intracellular stores and Ca2+ entry, respectively. When the histamine H-1 antagonist chlorpheniramine was added after the histamine-induced transient increase in [Ca2+](i), the Ca2+ entry induced by the addition of Ca2+ was inhibited. In the fibroblasts pretreated with cyclooxygenase inhibitors, indomethacin (1 mu M) or aspirin (100 mu M), histamine-induced Ca2+ entry was significantly inhibited, but not the transient [Ca2+](i) increase. These results suggest that the histamine-induced Ca2+ entry requires the continuous binding of histamine to the H-1 receptors and is regulated by prostaglandins, which are probably produced due to the H-1 receptor activation. (C) 1998 Elsevier Science Inc. [References: 20]
机译:在缺乏外部Ca2 +的情况下,100μM组胺引起细胞内Ca2 +([Ca2 +](i))的瞬时增加,随后向培养基中添加Ca2 +导致呋喃中Ca [2 +](i)的持续增加。 2次加载的人类牙龈成纤维细胞。这些Ca2 +动员分别归因于Ca2 +从细胞内储存的释放和Ca2 +的进入。当在组胺诱导的[Ca2 +](i)瞬时增加后添加组胺H-1拮抗剂扑尔敏时,由于添加Ca2 +引起的Ca2 +进入受到抑制。在用环氧合酶抑制剂,吲哚美辛(1μM)或阿司匹林(100μM)预处理的成纤维细胞中,组胺诱导的Ca2 +进入被显着抑制,但瞬时[Ca2 +](i)却没有增加。这些结果表明,组胺诱导的Ca2 +进入需要组胺与H-1受体的连续结合,并受到前列腺素的调节,而前列腺素可能是由于H-1受体的活化而产生的。 (C)1998 Elsevier Science Inc. [参考:20]

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