Abstract |
There is snowballing evidence that type 2 diabetes (T2D) predisposes to neuropathophysiological alterations including oxidative stress and triggered inflammatory responses in brain that eventually culminates into cognitive impairment.Accumulating evidences suggest that SGLT2 inhibitor can be a promising intervention for cognitive decline in T2DM. In the present paper, the potential effects of Empagliflozin (EMPA), a SGLT2 inhibitor, against T2D induced cognitive dysfunction have been explored. The effect of EMPA on array of inflammatory mediators including Interleukin-6(IL-6), Interleukin -1β (IL-1β), and Tumour necrosis factor-α(TNF-α)), neuronal proteins including glycogen synthase kinase-3β (GSK- 3β), Phosphorylated tau (p-tau), amyloid beta (Aβ) (1-40, 1-42) and altered oxidative parameters including SOD, catalase, TBARS was determined in the high fructose diet induced hyperglycaemic mice. The obtained results were compared with EMPA nanoparticles (Nps) formulated in our laboratory and found that EMPA Nps significantly showed reduced levels of inflammatory mediators and oxidative stress. Further, decrease in levels of p-tau, Aβ (1-40) and Aβ (1-42) were also observed with EMPA nanoparticles.Thus, the study has demonstrated that EMPA Nps could be a promising therapy to alleviate the progression of cognitive decline in T2D.
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Authors | Tahira Khan, Sana Khan, Mohd Akhtar, Javed Ali, Abul Kalam Najmi |
Journal | Neurochemistry international
(Neurochem Int)
Vol. 150
Pg. 105158
(11 2021)
ISSN: 1872-9754 [Electronic] England |
PMID | 34391818
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2021 Elsevier Ltd. All rights reserved. |
Chemical References |
- Benzhydryl Compounds
- Blood Glucose
- Glucosides
- Inflammation Mediators
- Sodium-Glucose Transporter 2 Inhibitors
- Fructose
- empagliflozin
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Topics |
- Animals
- Benzhydryl Compounds
(administration & dosage)
- Blood Glucose
(drug effects, metabolism)
- Cognitive Dysfunction
(chemically induced, metabolism, prevention & control)
- Diabetes Mellitus, Type 2
(chemically induced, metabolism, prevention & control)
- Fructose
(administration & dosage, toxicity)
- Glucosides
(administration & dosage)
- Hyperglycemia
(chemically induced, metabolism, prevention & control)
- Inflammation Mediators
(antagonists & inhibitors, metabolism)
- Mice
- Mice, Inbred C57BL
- Nanoparticles
(administration & dosage)
- Oxidative Stress
(drug effects, physiology)
- Sodium-Glucose Transporter 2 Inhibitors
(administration & dosage)
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