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Acta Pharmacologica Sinica 2005 February; 26 (2): 220-222; doi: 10.1111/j.1745-7254.2005.00527.x |
| Original Article | [ Full text ] |
| Swietenia mahagony extract shows agonistic activity to PPARγ and gives ameliorative effects on diabetic db/db mice |
| Dan-dan LI1,2,5, Jun-hua CHEN1,4,5, Qing CHEN1,4,
Guo-wei LI1,4, Jing CHEN1,4, Jian-min YUE1,4,
Min-li CHEN3, Xiao-ping WANG2, Jian-hua SHEN1,4,6,
Xu SHEN1,4,6, Hua-liang JIANG1,4,6 1Drug Discovery and Design Center, State Key Lab of Drug
Research, Shanghai Institute of Materia Medica, Shanghai Institutes for Biological
Sciences, Chinese Academy of Sciences, Shanghai 201203, 2Chemistry
Department, Tongji University, Shanghai 200092, 3Animal Experiment
Center, Zhejiang College of Traditional Chinese Medicine, Hangzhou 310053; 4Graduate
School of the Chinese Academy of Sciences, China
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Aim: To search the peroxisome proliferator-activated receptor γ (PPARγ) agonists from Swietenia mahagony extract (SmE) and observe the possible ameliorative effects of SmE on diabetic db/db mice.
Results: By using the clinical drug rosiglitazone as a positive control, it was found that the PPARγ agonistic activity of SmE at a concentration of 50 µg/L was approximately half that of 35.7 µg/L (0.1 µmol/L) of rosiglitazone. At the dose of 1000 mg/kg, SmE remarkably decreased the blood glucose concentration of db/db mice from (15.26±2.98) to (7.58±2.20) mmol/L, and reduced the blood glucose levels by 55.49% compared with the control group (P<0.01). Conclusion: SmE shows agonistic activity to PPARγ and can ameliorate the blood glucose levels of diabetic db/db mice. SmE may be thus used as a potential agent for diabetes therapy. |
Keywords: Swietenia mahagony; diabetes mellitus; peroxisome proliferator-activated receptor γ; yeast-two hybrid |
| 5 These authors contributed equally to this work. 6 Correspondence to Prof Jian-hua SHEN E-mail jhshen@mail.shcnc.ac.cn; Prof Xu SHEN E-mail xshen@mail.shcnc.ac.cn; Prof Hua-liang JIANG hljiang@mail.shcnc.ac.cn Phn 86-21-5080-6600. Fax 86-21-5080-7088. |
| Received 2004-09-24 Accepted 2004-11-09 | [ Full text ] |
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