Journal: |
Brazilian Journal of Biology
Brazilian Journal of Biology
|
Volume: |
|
Abstract: |
Diabetic nephropathy (DN) is a prevalent diabetic microvascular condition. It is the leading cause of kidney disease in
the advanced stages. There is no currently effective treatment available. This research aimed to investigate the curative
potentials of exosomes isolated from mesenchymal stem cells affecting DN. This study was performed on 70 male adult
albino rats. Adult rats were randomized into seven groups: Group I: Negative control group, Group II: DN group, Group
III: Balanites treated group, Group IV: MSCs treated group, Group V: Exosome treated group, Group VI: Balanites + MSCs
treated group and Group VII: Balanites + exosome treated group. Following the trial period, blood and renal tissues were
subjected to biochemical, gene expression analyses, and histopathological examinations. Results showed that MDA was
substantially increased, whereas TAC was significantly decreased in the kidney in the DN group compared to normal
health rats. Undesired elevated values of MDA levels and a decrease in TAC were substantially ameliorated in groups
co-administered Balanites aegyptiacae with MSCs or exosomes compared to the DN group. A substantial elevation
in TNF-α and substantially diminished concentration of IGF-1 were noticed in DN rats compared to normal health
rats. Compared to the DN group, the co-administration of Balanites aegyptiacae with MSCs or exosomes substantially
improved the undesirable elevated values of TNF-α and IGF-1. Furthermore, in the DN group, the mRNA expression of
Vanin-1, Nephrin, and collagen IV was significantly higher than in normal healthy rats. Compared with DN rats, Vanin-1,
Nephrin, and collagen IV Upregulation were substantially reduced in groups co-administered Balanites aegyptiacae with
MSCs or exosomes. In DN rats, AQP1 expression was significantly lower than in normal healthy rats. Furthermore, the
groups co-administered Balanites aegyptiacae with MSCs or exosomes demonstrated a substantial increase in AQP1
mRNA expression compared to DN rats.
|
|
|