Abstract

The antidiabetic effect and mode of action of Socrpio maurus palmatus body extract were evaluated in diabetic mice induced by alloxan. 24 male albino mice were divided into four groups. Group 1 was injected intraperitoneally with physiological saline. Group 2 was injected (i.p., daily for 5 weeks) with 300 mg/kg of the scorpion aqueous extract. Group 3 was received alloxan (150 mg/kg, i.p). Group 4 was diabetic and treated with scorpion extract (300 mg/kg, i.p., daily for 5 weeks). Several relevant biochemical parameters and histological examination of Langerhans islets were evaluated. The administration of scorpion extract significantly elevated the level of plasma insulin which was concomitant with a remarkable decrease in the level of blood glucose in diabetic mice. Furthermore, scorpion extract showed a notable ameliorative effect through enhancing the status of antioxidants and recovering the altered biochemical parameters in diabetic mice. Interestingly, scorpion extract significantly increased the number of β-cells and the size of pancreatic islets in diabetic mice. Accordingly, the obtained results demonstrate the antidiabetic effect of scorpion extract in alloxan-induced diabetic mice through its antioxidant and regeneration capacity.

Highlights

  • The lifelong progressive disease of diabetes mellitus (DM, one of the major causes of morbidity and death) is a chronic metabolic disturbance

  • There was a significant decrease in the level of blood glucose in the diabetic group treated with scorpion extract (p < 0.05)

  • Alloxan has a strong necrotizing effect on β-cells via its specific suppression of glucokinase and generation of ROS reduction of β-cells number resulted in insulin deficiency followed by various metabolic disorders in carbohydrates, proteins and fats [38]

Read more

Summary

Introduction

The lifelong progressive disease of diabetes mellitus (DM, one of the major causes of morbidity and death) is a chronic metabolic disturbance. Xie and colleagues reported that scorpion extract (Buthus martensii kirsch) combined with gypsum revealed a novel antidiabetic activity in diabetic mice (induced by streptozotocin) through upregulating the expression of pancreatic PPARγ (peroxisome proliferator-activated receptor gamma) and PDX-1 (pancreatic and duodenal homeobox 1), improving islet regeneration and enhancing insulin secretion [3]. In this regard, more investigations are urgently needed to develop therapeutic agents able to protect or regenerate pancreatic beta cells

Methods
Results
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.