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The Experimental Study on Treatment of Glucocorticoid-Induced Ischemic Necrosis of Femoral Head by Gu Fu Sheng Capsule 被引量:15

The Experimental Study on Treatment of Glucocorticoid-Induced Ischemic Necrosis of Femoral Head by Gu Fu Sheng Capsule
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摘要 Objective: To observe the effects of Gu Fu Sheng Capsule (骨复生胶囊 GFSC) on nitric oxide (NO) level and fibrinolytic activity in rabbits with glucocorticoid-induced ischemic necrosis of femoral head (GINFH)so as to explain the therapeutic mechanism of GFSC Methods: 48 rabbits were randomly divided into 4 The models of GINFH were produced by injection of glucocorticoid hormone for 8 weeks. From the 9th week, GFSC decoction was given to the rabbits of the group A (45g. kg-1 d-1) and MSGP extract was given to the group B (0.17 g kg-1 d-1) and the same volume of normal saline to group C and D by intragastric infusion. The content of plasma nitric oxide (NO), and activities of tissue-type plasminogen activator (t-PA), and plasminogen activator inhibitor (PAI) were detected after the hormone was injected for 4 and 8 weeks and after the drugs were given for 4 weeks. Results: Compared with the group D, the contents of NO and t-PA activity in the group C decreased significantly (P<0.01), but the activity of PAI increased significantly (P<0.01). Compared with the group C, the contents of NO and t-PA activity in the group A and B increased significantly (P<0.05), but the activity of PAI decreased significantly (P<0.05), with no significant difference between the two treatment groups (P>0.05). Conclusion: GFSC could increase the level of NO, protect endotheolial cells and improve fibrinolytic activity, which might be the mechanism of GFSC in curing GINFH. Objective:To observe the effects of Gu Fu Sheng Capsule(骨复生胶囊 GFSC)on nitric oxide(NO)level and fibrinolytic activity in rabbits with glucocorticoid-induced ischemic necrosis of femoral head(GINFH) so as to explain the therapeutic mechanism of GFSC.Methods:48 rabbits were randomly divided into 4 groups:GFSC group A,Ma Shi Gu Pian(马氏骨片 MSGP)group B,model group C,and control group D. The models of GINFH were produced by injection of glucocorticoid hormone for 8 weeks.From the 9th week,GFSC decoction was given to the rabbits of the group A(45g·kg^(-1)·d^(-1))and MSGP extract was given to the group B(0.17 g kg^(-1)·d^(-1))and the same volume of normal saline to group C and D by intragastric infusion.The content of plasma nitric oxide(NO),and activities of tissue-type plasminogen activator (t-PA),and plasminogen activator inhibitor(PAI)were detected after the hormone was injected for 4 and 8 weeks and after the drugs were given for 4 weeks.Results:Compared with the group D,the contents of NO and t-PA activity in the group C decreased significantly(P<0.01),but the activity of PAI increased significantly(P<0.01).Compared with the group C,the contents of NO and t-PA activity in the group A and B increased significantly(P<0.05),but the activity of PAI decreased significantly(P<0.05),with no significant difference between the two treatment groups(P>0.05).Conclusion:GFSC could increase the level of NO,protect endotheolial cells and improve fibrinolytic activity,which might be the mechanism of GFSC in curing GINFH.
出处 《Journal of Traditional Chinese Medicine》 SCIE CAS CSCD 2004年第4期303-307,共5页 中医杂志(英文版)
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