Redox TRPs in diabetes and diabetic complications: Mechanisms and pharmacological modulation

Pratik Adhya1, Shyam Sunder Sharma1

  • 1Department of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Sector 67, S.A.S. Nagar, Mohali, 160 062, Punjab, India.

Insights

Redox-sensitive Transient Receptor Potential (TRP) channels are implicated in diabetes complications. Targeting these redox TRP channels offers a promising therapeutic strategy for managing diabetes and its associated conditions.

Area of Science:

  • Physiology
  • Pharmacology
  • Molecular Biology

Background:

  • Transient Receptor Potential (TRP) channels regulate diverse physiological functions and are implicated in numerous diseases.
  • Diabetes mellitus, a global epidemic, is exacerbated by hyperglycemia-induced oxidative stress.
  • Redox TRP channels, which sense and respond to cellular redox environments, are modulated by oxidative stress in diabetes.

Purpose of the Study:

  • To review the role of redox-sensing TRP channels in diabetes and its complications.
  • To explore the potential of targeting redox TRPs as a novel therapeutic strategy.

Main Methods:

  • Literature review of studies investigating TRP channels in diabetes.
  • Analysis of the impact of oxidative stress on redox TRP channel activity.
  • Discussion of pharmacological modulation of redox TRPs.

Main Results:

  • Specific redox TRP channels (TRPA1, TRPC5, TRPMs, TRPV1) are modulated by diabetes-induced oxidative stress.
  • Dysregulation of these channels contributes to diabetic complications such as neuropathy, cardiomyopathy, retinopathy, cystopathy, and encephalopathy.

Conclusions:

  • Redox TRP channels represent a significant therapeutic target for diabetes and its associated complications.
  • Pharmacological targeting of these channels may offer novel treatment avenues.

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