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Nigella sativa L. and its bioactive and nutraceutical components in the management of diabetic peripheral neuropathy.
- Source :
-
Inflammopharmacology [Inflammopharmacology] 2024 Oct; Vol. 32 (5), pp. 2897-2920. Date of Electronic Publication: 2024 Aug 14. - Publication Year :
- 2024
-
Abstract
- Diabetes-induced hyperglycemia leads to excessive production of oxygen free radicals, inflammatory cytokines, and oxidative stress, which initiates diabetic peripheral neuropathy (DPN). Currently, this condition affects 20% of adults with diabetes. Despite significant advances in the treatment of diabetes, the incidence of its complications, including DPN, is still high. Thus, there is a growing research interest in developing more effective and treatment approaches with less side effects for diabetes and its complications. Nigella sativa L. (NS) has received much research attention as an antioxidant, anti-yperglycemic factor, and anti-inflammatory agent. This natural compound demonstrates its antidiabetic neuropathy effect through various pathways, including the reduction of lipid peroxidation, the enhancement of catalase and superoxide dismutase enzyme activity, and the decrease in inflammatory cytokine levels. The present review focuses on the bioactive and nutraceutical components of black cumin (Nigella sativa L.) and their effects on DPN. In addition, we have also summarized the findings obtained from several experimental and clinical studies regarding the antidiabetic neuropathy effect of NS in animal models and human subjects.<br /> (© 2024. The Author(s), under exclusive licence to Springer Nature Switzerland AG.)
- Subjects :
- Humans
Animals
Oxidative Stress drug effects
Anti-Inflammatory Agents pharmacology
Diabetic Neuropathies drug therapy
Diabetic Neuropathies metabolism
Nigella sativa chemistry
Dietary Supplements
Hypoglycemic Agents pharmacology
Hypoglycemic Agents therapeutic use
Antioxidants pharmacology
Plant Extracts pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1568-5608
- Volume :
- 32
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Inflammopharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 39143432
- Full Text :
- https://doi.org/10.1007/s10787-024-01528-6