Protein Kinase C (PKC)-mediated TGF-β Regulation in Diabetic Neuropathy: Emphasis on Neuro-inflammation and Allodynia

Endocr Metab Immune Disord Drug Targets. 2024;24(7):777-788. doi: 10.2174/0118715303262824231024104849.

Abstract

According to the World Health Organization (WHO), diabetes has been increasing steadily over the past few decades. In developing countries, it is the cause of increased morbidity and mortality. Diabetes and its complications are associated with education, occupation, and income across all levels of socioeconomic status. Factors, such as hyperglycemia, social ignorance, lack of proper health knowledge, and late access to medical care, can worsen diabetic complications. Amongst the complications, neuropathic pain and inflammation are considered the most common causes of morbidity for common populations. This review is focused on exploring protein kinase C (PKC)-mediated TGF-946; regulation in diabetic complications with particular emphasis on allodynia. The role of PKC-triggered TGF-946; in diabetic neuropathy is not well explored. This review will provide a better understanding of the PKC-mediated TGF-946; regulation in diabetic neuropathy with several schematic illustrations. Neuroinflammation and associated hyperalgesia and allodynia during microvascular complications in diabetes are scientifically illustrated in this review. It is hoped that this review will facilitate biomedical scientists to better understand the etiology and target drugs effectively to manage diabetes and diabetic neuropathy.

Keywords: Diabetes; allodynia.; diabetic complications; neuropathy; protein kinase C (PKC); transforming growth factor 946; (TGF-946;).

Publication types

  • Review

MeSH terms

  • Animals
  • Diabetic Neuropathies* / drug therapy
  • Diabetic Neuropathies* / metabolism
  • Humans
  • Hyperalgesia* / metabolism
  • Neuroinflammatory Diseases* / metabolism
  • Protein Kinase C* / metabolism
  • Signal Transduction / physiology
  • Transforming Growth Factor beta* / metabolism

Substances

  • Protein Kinase C
  • Transforming Growth Factor beta