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Mitochondrial dysfunction and beneficial effects of mitochondria-targeted small peptide SS-31 in Diabetes Mellitus and Alzheimer's disease

Journal

PHARMACOLOGICAL RESEARCH
Volume 171, Issue -, Pages -

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.phrs.2021.105783

Keywords

Mitochondria; Diabetes; Alzheimer's disease; SS peptide; SS-31

Funding

  1. Alabama Agricultural Experimental Station (AAES), Hatch/Multistate Funding Program
  2. AAES Award for Interdisciplinary Research (AAES-AIR)

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The article discusses the pathophysiological relevance of mitochondria in Diabetes and Alzheimer's disease, as well as the potential therapeutic benefits of Szeto-Schiller-31 peptide in treating these conditions.
Diabetes and Alzheimer's disease are common chronic illnesses in the United States and lack clearly demonstrated therapeutics. Mitochondria, the powerhouse of the cell, is involved in the homeostatic regulation of glucose, energy, and reduction/oxidation reactions. The mitochondria has been associated with the etiology of metabolic and neurological disorders through a dysfunction of regulation of reactive oxygen species. Mitochondria-targeted chemicals, such as the Szeto-Schiller-31 peptide, have advanced therapeutic potential through the inhibition of oxidative stress and the restoration of normal mitochondrial function as compared to traditional antioxidants, such as vitamin E. In this article, we summarize the pathophysiological relevance of the mitochondria and the beneficial effects of Szeto-Schiller-31 peptide in the treatment of Diabetes and Alzheimer's disease.

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