Abstract | OBJECTIVES: METHODS: KEY FINDINGS: Treatment with caffeic acid significantly decreased blood glucose levels and elevated serum insulin levels while improving glucose tolerance, pancreatic β-cell function and morphology. It also led to a significant reduction of serum cholesterol, triglyceride, LDL-cholesterol, ALT, AST, creatinine, urea and uric acid levels, while increasing HDL cholesterol levels. Caffeic acid significantly (P < 0.05) elevated hepatic glycogen level, serum and pancreatic glutathione level, superoxide dismutase and catalase activities with a concomitant decrease in malondialdehyde level, α- amylase, lipase, adenosine triphosphatase ( ATPase), ectonucleoside triphosphate diphosphohydrolase (ENTPDase), 5'-nucleotidase (5'-NTD) and acetylcholinesterase activities. CONCLUSION: The results suggest caffeic acid as a potent natural product with therapeutic effects against T2D. Further molecular and clinical studies are, however, required to ascertain these findings.
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Authors | Veronica F Salau, Ochuko L Erukainure, Omamuyovwi M Ijomone, Md Shahidul Islam |
Journal | The Journal of pharmacy and pharmacology
(J Pharm Pharmacol)
Vol. 74
Issue 7
Pg. 973-984
(Jul 15 2022)
ISSN: 2042-7158 [Electronic] England |
PMID | 35640634
(Publication Type: Journal Article)
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Copyright | © The Author(s) 2022. Published by Oxford University Press on behalf of the Royal Pharmaceutical Society. All rights reserved. For permissions, please e-mail: [email protected]. |
Chemical References |
- Blood Glucose
- Caffeic Acids
- Cholinergic Agents
- Hypoglycemic Agents
- Plant Extracts
- Fructose
- Streptozocin
- Cholesterol
- Acetylcholinesterase
- caffeic acid
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Topics |
- Acetylcholinesterase
- Animals
- Blood Glucose
- Caffeic Acids
(pharmacology)
- Cholesterol
- Cholinergic Agents
- Diabetes Mellitus, Experimental
(drug therapy)
- Diabetes Mellitus, Type 2
(chemically induced, drug therapy)
- Dyslipidemias
(chemically induced, drug therapy)
- Fructose
(adverse effects)
- Homeostasis
- Hypoglycemic Agents
(therapeutic use)
- Male
- Oxidative Stress
- Plant Extracts
(pharmacology)
- Rats
- Rats, Sprague-Dawley
- Streptozocin
(pharmacology)
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