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TRPV1: A novel target for the therapy of diabetes and diabetic complications

Yu-Rong Shen1, Long Cheng1, Dong-Fang Zhang1

  • 1Department of Pharmacognosy, School of Pharmacy, China Medical University, Shenyang 110122, China.

PubMed
Abstract

Insights

Transient receptor potential vanilloid-1 (TRPV1) shows promise for treating diabetes and its complications by regulating glucose production and metabolism. This review explores TRPV1

Area of Science:

  • Pharmacology
  • Endocrinology
  • Molecular Biology

Background:

  • Diabetes mellitus, particularly Type II, is a chronic condition with inadequate current therapies.
  • Existing treatments for hyperglycemia do not prevent disease progression or associated complications like neuropathy and retinopathy.
  • Developing novel, effective, and safe glucose-lowering methods is crucial.

Purpose of the Study:

  • To systematically review the mechanism of action of the TRPV1 signaling pathway in diabetes.
  • To explore the potential of TRPV1 as a therapeutic target for diabetes and its complications.
  • To provide a basis for developing new TRPV1-targeted hypoglycemic drugs.

Main Methods:

  • Conducted a literature search across major databases (PubMed, Web of Science, Google Scholar, Medline, Scopus).
  • Focused on studies published between 2013 and 2023.
  • Utilized keywords: "diabetes," "TRPV1," "diabetic complications," and "capsaicin."

Main Results:

  • TRPV1 activation reduces hepatic glucose production, decreases food intake, and enhances thermogenesis, metabolism, and insulin secretion.
  • TRPV1 activation ameliorates various diabetic complications including nephropathy, retinopathy, myocardial infarction, and vascular dysfunction.
  • TRPV1 modulation shows potential for osteoporosis and certain neuropathies, though effects can vary.

Conclusions:

  • TRPV1 represents a significant therapeutic target for managing diabetes mellitus and its associated complications.
  • This review establishes a theoretical foundation for the development of novel hypoglycemic agents targeting the TRPV1 pathway.

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