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Antidiabetic effect of Ruta montana L. in streptozotocin-induced diabetic rats

  • Omar Farid , Morad Hebi , Mohammed Ajebli , Ahmed EL Hidani and Mohamed Eddouks EMAIL logo
Published/Copyright: January 25, 2017

Abstract

Background:

Ruta montana (L.) is known as a medicinal plant with many beneficial effects, including those that can be used in the treatment of diabetes. The objective of the study was to investigate the antidiabetic effect of this plant in diabetic rat.

Methods:

This study investigated the effects of an aerial part aqueous extract (APAE) of Ruta montana (L.) (RM) at a dose of 5 mg/kg on blood glucose levels in normal and streptozotocin (STZ)-induced diabetic rats. Histopathological changes were also evaluated in liver and pancreas both in normal and STZ-induced rats. The effect of this aqueous extract on glucose tolerance was demonstrated in normal rats. Furthermore, the relative organ weight (ROW) of liver, kidney, pancreas, and brown adipose tissue were evaluated after 15 days of daily oral administration of the aqueous extract.

Results:

Both single and repeated oral doses of APAE (5 mg/kg) produced significant reductions in the blood glucose levels in normal and STZ-induced rats. Oral glucose tolerance test results showed that, after the administration of 3 g/kg of glucose, RM APAE (5 mg/kg) improved the increase in blood glucose levels in normal rats at the 30th min (p<0.01) and 90th min (p<0.001).

Conclusions:

RM APAE exhibits a potent hypoglycemic effect in normal rats and an antidiabetic effect in STZ-induced rats. This finding supports the use of this plant in traditional Moroccan medicine for diabetes management.


Corresponding author: Professor Mohamed Eddouks, Faculty of Sciences and Techniques Errachidia, Moulay Ismail University, Boutalamine, BP 21, Errachidia, 52000, Morocco, Phone: +212 55 57 44 97, Fax: +212 55 57 44 85

Acknowledgments

This work was supported by the CNRST under Grant No. PPR/2015/35.

  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved its submission.

  2. Research funding: None declared.

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

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Received: 2016-3-5
Accepted: 2016-10-26
Published Online: 2017-1-25
Published in Print: 2017-5-1

©2017 Walter de Gruyter GmbH, Berlin/Boston

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