Abstract
Aim:
To reinvestigate the characteristics of reserpine-induced gastric mucosal lesions (GMLs).
Methods:
The GML-inducing effect of reserpine and the time-course of recovery from reserpine-induced GMLs were examined in Sprague-Dawley (SD) rats. The GML-inducing and blood pressure-decreasing effects of Compound Hypotensive Tablets (CHTs) were investigated in spontaneously hypertensive rats (SHRs). Intracerebroventricular (icv) injection and vagotomy were performed to verify the central vagal mechanism in reserpine-induced GMLs.
Results:
Single intraperitoneal (ip) injections of reserpine (0.25, 0.5, 1, 2, 4, and 6 mg/kg) dose-dependently induced GMLs in SD rats. Both single and repeated (2 weeks) oral administrations of reserpine led to slight GMLs at doses of 24 mg/kg and 10 mg/kg, respectively. Blood pressure was significantly decreased in SHRs after 2 months of CHT administration (0.01 and 0.03 mg/kg; doses were expressed as the amount of reserpine in the CHT). CHT doses of 0.3 mg/kg induced GMLs, but 0.1 mg/kg did not. Examining the time course of recovery from GMLs, severe GMLs occurred 18 h after ip reserpine (4 mg/kg), obviously lessened at 1 week and healed spontaneously at 3 weeks. Intracerebroventricular injections of reserpine caused GMLs at much lower doses (0.08 and 0.4 mg/kg), and reserpine-induced GMLs were greatly inhibited by vagotomy, suggesting the involvement of a central vagal mechanism.
Conclusion:
Reserpine-induced GMLs were dose-dependent, and the lesions healed spontaneously within 3 weeks. Long-term treatment with CHT at doses adequate to decrease blood pressure will not induce GMLs. A central vagal mechanism was involved in reserpine-induced GMLs.
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Acknowledgements
This study was supported by grants from the National Science and Technology Major Project (No 2009ZX09303-002), the China Postdoctoral Science Foundation Funded Project (No 20080441303) and the Shanghai Postdoctoral Sustentation Fund (No 08R214101).
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Ma, Xj., Lu, Gc., Song, Sw. et al. The features of reserpine-induced gastric mucosal lesions. Acta Pharmacol Sin 31, 938–943 (2010). https://doi.org/10.1038/aps.2010.74
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DOI: https://doi.org/10.1038/aps.2010.74
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