Reddy G K, Dhar S C
Department of Biochemistry, Central Leather Research Institute, Madras, India.
Ital J Biochem. 1987 Jul-Aug;36(4):205-17.
The effect of new non-steroidal anti-inflammatory agents on lysosomal stability was studied by determining the activity of beta-glucuronidase, a typical lysosomal enzyme, in various sub-cellular fractions and its release from the lysosome-rich fraction. Adjuvant arthritic animals showed a significant increase in the beta-glucuronidase activity in sub-cellular fractions. The increased rate of the release of beta-glucuronidase from lysosome-rich fraction clearly suggested that arthritic syndrome caused decreased stability of the lysosomes. Administration of boswellic acids or salai-guggal to arthritic animals was found to increase the lysosomal stability by inhibiting the rate of release from lysosome-rich fraction and reducing beta-glucuronidase activity in various sub-cellular fractions. Of the two anti-inflammatory agents tested, salai-guggal was found to afford more therapeutic value than boswellic acids.
通过测定β-葡萄糖醛酸酶(一种典型的溶酶体酶)在各种亚细胞组分中的活性及其从富含溶酶体的组分中的释放,研究了新型非甾体抗炎药对溶酶体稳定性的影响。佐剂性关节炎动物的亚细胞组分中β-葡萄糖醛酸酶活性显著增加。β-葡萄糖醛酸酶从富含溶酶体的组分中释放的增加速率清楚地表明,关节炎综合征导致溶酶体稳定性降低。发现给关节炎动物施用乳香酸或娑罗子可通过抑制从富含溶酶体的组分中的释放速率并降低各种亚细胞组分中的β-葡萄糖醛酸酶活性来提高溶酶体稳定性。在所测试的两种抗炎药中,发现娑罗子比乳香酸具有更高的治疗价值。