The antinociceptive activity of Muntingia calabura aqueous extract and the involvement of L-arginine/nitric oxide/cyclic guanosine monophosphate pathway in its observed activity in mice

被引:21
|
作者
Zakaria, Zainul Amiruddin
Sulaiman, Mohd Roslan
Jais, Abdul Manan Mat
Somchit, Muhammad Nazrul
Jayaraman, Kogilla Vani
Balakhrisnan, Ganesh
Abdullah, Fatimah Corazon
机构
[1] Univ Ind Selangor, Sch Biotechnol & Life Sci, Shah Alam 40000, Selangor, Malaysia
[2] Univ Putra Malaysia, Dept Biomed Sci, Fac Med & Hlth Sci, Serdang 43400, Malaysia
关键词
abdominal constriction test; antinociception; aqueous extract; L-arginine/nitric oxide/cyclic guanosine monophosphate pathway; Muntingia calabura;
D O I
10.1111/j.1472-8206.2006.00412.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The present study was carried out to investigate on the possible involvement of L-arginine/nitric oxide/cyclic guanosine monophosphate (L-arginine/NO/cGMP) pathway in the aqueous extract of Muntingia calabura (AEMC) leaves antinociception in mice assessed by abdominal constriction test. The AEMC, obtained by soaking the dried leaves in distilled water (DH2O) (1 : 2; w/v) for 24 h, was prepared in concentrations of 10%, 50% and 100% that were approximately equivalent to doses of 27, 135 and 270 mg/kg, and administered subcutaneously (s.c.) 5 min after pre-treatment (s.c.) of mice with DH2O, L-arginine (20 mg/kg), N-G-monomethyl-L-arginine acetate (L-NMMA; 20 mg/kg), N-G-nitro-L-arginine methyl esters (L-NAME; 20 mg/kg), methylene blue (MB) (20 mg/kg), respectively. The AEMC was found to exhibit a concentration-dependent antinociception after pre-challenge with DH2O. Interestingly, pre-treatment with L-arginine was found to block significantly (P < 0.05) the AEMC antinociception but only at the highest concentration (100%) of AEMC used. On the other hand, pre-treatment with L-NAME was found to significantly (P < 0.05) enhance the low concentration but inhibit the high concentration AEMC antinociception. MB was found to significantly (P < 0.05) enhance AEMC antinociception at all concentrations used. Except for the higher concentration of AEMC used, co-treatment with L-NAME was found to insignificantly and significantly (P < 0.05) reverse the L-arginine effect when given alone or with low concentration AEMC, respectively. In addition, co-treatment with MB significantly (P < 0.05) reversed the L-arginine effect when given alone or with 10% concentration AEMC but failed to affect the activity of the rest of concentrations used. As a conclusion, this study has demonstrated the involvement of L-arginine/NO/cGMP pathway in AEMC antinociception.
引用
收藏
页码:365 / 372
页数:8
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