Effect of insulin-loaded trimethyl chitosan nanoparticles on genes expression in the hippocampus of diabetic rats

Author:

Kalantarian Giti1,Ziamajidi Nasrin1,Abbasalipourkabir Roghayeh1,Mahjub Reza2,Goodarzi Mohammad Taghi3,Saidijam Massoud4,Soleimani Asl Sara5,Jamshidi Mohammad6

Affiliation:

1. Department of Biochemistry, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran

2. Department of Pharmaceutics, School of Pharmacy, Hamadan University of Medical Sciences, Hamadan, Iran

3. Department of Biochemistry, Shahrood Branch, Islamic Azad University, Shahrood, Iran

4. Research Center for Molecular Medicine, Hamadan University of Medical Sciences, Hamadan, Iran

5. Endometrium and Endometriosis Research Centre, Hamadan University of Medical Sciences, Hamadan, Iran

6. Department of Laboratory Sciences, School of Allied Medicine, Lorestan University of Medical Sciences, Khorramabad, Iran

Abstract

AbstractBackgroundDiabetes mellitus is a chronic metabolic disorder that undesirably affects both central and peripheral nervous systems through the apoptosis of neurons. Insulin and insulin-like growth factors (IGFs) inhibit apoptosis of oligodendrocytes. The objective of this study was to determine whether oral insulin in the form of nanoparticles may have similar effects to injectable insulin in increasing the gene expression ofIGF1andIGF2.MethodsInsulin-loaded trimethyl chitosan nanoparticles were prepared using the polyelectrolyte complex method and characterized for size, polydispersity index, zeta potential, drug loading, and entrapment efficiency. Anin vivostudy was performed in different groups of male Wistar rats with diabetes mellitus type 1 treated with insulin-loaded trimethyl chitosan nanoparticles and subcutaneous injection of trade insulin (neutral protamine Hagedorn). The hippocampus of rats were studied for the expression ofIGF1andIGF2genes by using real-time PCR, and the fold changes in gene expression were evaluated using the 2−ΔΔCtmethod.ResultsThe expression ofIGF1andIGF2genes in the groups treated with nano-insulin and injected insulin were significantly higher than that in the diabetic control group (p<0.001) and meaningfully lower than that in the healthy control group. However, there was no significant difference to the treated groups.ConclusionOur findings suggest that future research might provide a new formulation of drugs for treating type 1 diabetes, in the form of oral insulin.

Publisher

Walter de Gruyter GmbH

Subject

Drug Discovery,Pharmacology,General Medicine,Physiology

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