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拉扎罗ids(21-氨基类固醇)对成纤维细胞增殖的抑制作用。

Inhibition of proliferation of fibroblasts by lazaroids (21-aminosteroids).

作者信息

Singh J P, Bonin P D

机构信息

Cardiovascular Research, Lilly Research Laboratory, Indianapolis, IN 46285.

出版信息

Life Sci. 1991;49(26):2053-8. doi: 10.1016/0024-3205(91)90648-u.

Abstract

Lazaroids (21-aminosteroids) are a novel group of compounds that inhibit lipid peroxidation in biological systems and protect cells from oxidative damage during tissue injury. In vivo efficacy of lazaroids has been demonstrated in a variety of animal models of traumatic or ischemic injury of central nervous system (1-6). However, very little is known about the affects of lazaroids on cellular responses associated with tissue repair and remodeling eg cell proliferation and synthesis of extracellular matrix. In the present study, we show that lazaroids and certain related compounds inhibit cell proliferation in vitro. Light microscopic examination and determination of release of intracellular enzyme, lactate dehydrogenase suggested that cell growth inhibition by lazaroids was not due to cell death resulting from cytotoxic effects. Examination of several lazaroid related antioxidants and other known antioxidants eg vitamin E and Probucol showed that compounds with similar antioxidant potential did not exhibit identical antiproliferative activity, suggesting that cell growth inhibition by lazaroids may be unrelated to their antioxidant action. These results may have implication in the therapeutic actions of lazaroids.

摘要

拉扎罗类药物(21-氨基类固醇)是一类新型化合物,可抑制生物系统中的脂质过氧化,并在组织损伤期间保护细胞免受氧化损伤。拉扎罗类药物的体内疗效已在多种中枢神经系统创伤或缺血性损伤的动物模型中得到证实(1-6)。然而,关于拉扎罗类药物对与组织修复和重塑相关的细胞反应(如细胞增殖和细胞外基质合成)的影响,人们了解甚少。在本研究中,我们表明拉扎罗类药物和某些相关化合物在体外可抑制细胞增殖。光学显微镜检查和细胞内酶乳酸脱氢酶释放的测定表明,拉扎罗类药物对细胞生长的抑制并非由于细胞毒性作用导致的细胞死亡。对几种与拉扎罗类药物相关的抗氧化剂和其他已知抗氧化剂(如维生素E和普罗布考)的研究表明,具有相似抗氧化潜力的化合物并未表现出相同的抗增殖活性,这表明拉扎罗类药物对细胞生长的抑制可能与其抗氧化作用无关。这些结果可能对拉扎罗类药物的治疗作用具有启示意义。

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