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一种新型非甾体抗炎药——锯叶棕提取物的药理学

Pharmacology of an extract of salai guggal ex-Boswellia serrata, a new non-steroidal anti-inflammatory agent.

作者信息

Singh G B, Atal C K

出版信息

Agents Actions. 1986 Jun;18(3-4):407-12. doi: 10.1007/BF01965005.

Abstract

Pharmacological evaluation of alcoholic extract of salai guggal (AESG) has been carried out in experimental animals. AESG displayed marked anti-inflammatory activity in carrageenan induced oedema in rats and mice and dextran oedema in rats. It was equally effective in adrenalectomised rats. In formaldehyde and adjuvant arthritis, AESG produced prominent anti-arthritic activity but no significant effect was observed in cotton pellet-induced granuloma test. It inhibited inflammation induced increase in serum transaminase levels and leucocyte counts but lacked any analgesic or anti-pyretic effects. The gestation period or parturition time in pregnant rats or onset time of castor oil-induced diarrhoea was unaffected by AESG and no significant effect was seen on cardiovascular, respiratory and central nervous system functions. No ulcerogenic effects were found in the rat stomach. The oral and intraperitoneal LD50 was greater than 2 g/Kg in mice and rats.

摘要

已在实验动物中对萨莱古格(AESG)酒精提取物进行了药理学评估。AESG在角叉菜胶诱导的大鼠和小鼠水肿以及大鼠右旋糖酐水肿中显示出显著的抗炎活性。在肾上腺切除的大鼠中同样有效。在甲醛和佐剂性关节炎中,AESG产生了显著的抗关节炎活性,但在棉球诱导的肉芽肿试验中未观察到显著效果。它抑制炎症诱导的血清转氨酶水平和白细胞计数增加,但没有任何镇痛或解热作用。AESG对怀孕大鼠的妊娠期或分娩时间或蓖麻油诱导的腹泻发作时间没有影响,对心血管、呼吸和中枢神经系统功能也没有显著影响。在大鼠胃中未发现致溃疡作用。小鼠和大鼠的口服和腹腔内LD50均大于2 g/Kg。

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