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己酮可可碱可抑制源自瘢痕疙瘩、硬皮病和局限性硬皮病皮肤的人成纤维细胞的增殖及其胶原蛋白、糖胺聚糖和纤连蛋白的生成。

Pentoxifylline inhibits the proliferation of human fibroblasts derived from keloid, scleroderma and morphoea skin and their production of collagen, glycosaminoglycans and fibronectin.

作者信息

Berman B, Duncan M R

机构信息

Department of Dermatology, University of California, Davis School of Medicine.

出版信息

Br J Dermatol. 1990 Sep;123(3):339-46. doi: 10.1111/j.1365-2133.1990.tb06294.x.

Abstract

Pentoxifylline, an analogue of the methylxanthine theobromine, inhibits the proliferation and certain biosynthetic activities of fibroblasts derived from normal human skin. Fibroblasts from the skin of patients with keloids, scleroderma and morphoea were cultured in vitro in the presence and absence of pentoxifylline (100-1000 micrograms/ml) to determine whether it inhibits fibroblast proliferation and the production of collagen, glycosaminoglycans (GAG), fibronectin and collagenase activity. The exposure of subconfluent fibroblast cultures to pentoxifylline resulted in non-lethal, dose-dependent reductions in serum-driven fibroblast proliferation, with 1000 micrograms/ml pentoxifylline virtually negating the proliferative effect of serum on the cells. The fibroblasts assayed as confluent cultures produced reduced amounts, by up to 95%, of collagen and GAG, dependent on the concentration of pentoxifylline, both in the presence and absence of serum. Pentoxifylline similarly inhibited the fibronectin production by keloid and scleroderma fibroblasts, but had no effect on collagenase activity.

摘要

己酮可可碱是甲基黄嘌呤可可碱的类似物,可抑制源自正常人类皮肤的成纤维细胞的增殖及某些生物合成活性。在有和没有己酮可可碱(100 - 1000微克/毫升)存在的情况下,对瘢痕疙瘩、硬皮病和局限性硬皮病患者皮肤的成纤维细胞进行体外培养,以确定它是否抑制成纤维细胞增殖以及胶原蛋白、糖胺聚糖(GAG)、纤连蛋白的产生和胶原酶活性。将亚汇合的成纤维细胞培养物暴露于己酮可可碱会导致血清驱动的成纤维细胞增殖出现非致死性的剂量依赖性降低,1000微克/毫升的己酮可可碱几乎消除了血清对细胞的增殖作用。作为汇合培养物检测的成纤维细胞,无论有无血清,产生的胶原蛋白和GAG量均减少,最多可减少95%,这取决于己酮可可碱的浓度。己酮可可碱同样抑制瘢痕疙瘩和硬皮病成纤维细胞的纤连蛋白产生,但对胶原酶活性没有影响。

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