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新型草药抗炎剂作用下糖胺聚糖代谢的研究

Studies on the metabolism of glycosaminoglycans under the influence of new herbal anti-inflammatory agents.

作者信息

Reddy G K, Chandrakasan G, Dhar S C

机构信息

Department of Biochemistry, Central Leather Research Institute, Madras, India.

出版信息

Biochem Pharmacol. 1989 Oct 15;38(20):3527-34. doi: 10.1016/0006-2952(89)90124-x.

Abstract

The in vivo effect of an herbal based, non-steroidal anti-inflammatory product, salai guggal, prepared from the gum resin exudate of Boswellia serrata and its active principle "boswellic acids" on glycosaminoglycan metabolism has been studied in male albino rats. The biosynthesis of sulfated glycosaminoglycans, as evaluated by the uptake of [35S]sulfate, and the content of glycosaminoglycans were measured in specimens of skin, liver, kidney and spleen. Statistical analysis of the data obtained with respect to the boswellic acids and salai guggal were compared with those of ketoprofen. A significant reduction in glycosaminoglycan biosynthesis was observed in rats treated with all of the drugs. Glycosaminoglycan content was found to be decreased in the ketoprofen-treated group, whereas that of the boswellic acids or salai guggal treated groups remained unaltered. The catabolism of glycosaminoglycans was followed by estimating the activities of lysosomal glycohydrolases, namely beta-glucuronidase, beta-N-acetylglucosaminidase, cathepsin B1, cathepsin B2 and cathepsin D, in tissues and by estimating the urinary excretion and hexosamine and uronic acid. The degradation of glycosaminoglycans was found to be reduced markedly in all drug-treated animals as compared to controls. The potential significance of boswellic acids and salai guggal was discussed in the light of changes in the metabolism of glycosaminoglycans.

摘要

在雄性白化病大鼠中,研究了一种以草药为基础的非甾体抗炎产品——娑罗子古古勒(由乳香树树脂渗出物制备而成)及其活性成分“乳香酸”对糖胺聚糖代谢的体内作用。通过[35S]硫酸盐摄取评估硫酸化糖胺聚糖的生物合成,并测量皮肤、肝脏、肾脏和脾脏标本中糖胺聚糖的含量。将关于乳香酸和娑罗子古古勒所获得数据的统计分析结果与酮洛芬的数据进行比较。在用所有药物治疗的大鼠中,均观察到糖胺聚糖生物合成显著减少。在酮洛芬治疗组中,糖胺聚糖含量降低,而在乳香酸或娑罗子古古勒治疗组中,糖胺聚糖含量保持不变。通过估计组织中溶酶体糖苷水解酶(即β-葡萄糖醛酸酶、β-N-乙酰氨基葡萄糖苷酶、组织蛋白酶B1、组织蛋白酶B2和组织蛋白酶D)的活性,并估计尿中排泄的己糖胺和糖醛酸,来追踪糖胺聚糖的分解代谢。与对照组相比,在所有药物治疗的动物中,糖胺聚糖的降解均明显减少。根据糖胺聚糖代谢的变化,讨论了乳香酸和娑罗子古古勒的潜在意义。

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