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Ferulic acid promotes muscle glucose uptake and modulate dysregulated redox balance and metabolic pathways in ferric-induced pancreatic oxidative injury.
Salau, Veronica F; Erukainure, Ochuko L; Koorbanally, Neil A; Islam, Md Shahidul.
Affiliation
  • Salau VF; Department of Biochemistry, University of KwaZulu-Natal (Westville Campus), Durban, South Africa.
  • Erukainure OL; Department of Biochemistry, Veritas University, Bwari, Abuja, Nigeria.
  • Koorbanally NA; Department of Biochemistry, University of KwaZulu-Natal (Westville Campus), Durban, South Africa.
  • Islam MS; Department of Pharmacology, University of the Free State, Bloemfontein, South Africa.
J Food Biochem ; 46(4): e13641, 2022 04.
Article in En | MEDLINE | ID: mdl-33555086
The antidiabetic properties of ferulic acid and its protective role against Fe2+ -induced oxidative pancreatic injury were investigated in this study using in vitro and ex vivo models. Induction of oxidative injury in the pancreas was achieved by incubating normal pancreatic tissue with 0.1 mM FeSO4 and treated by co-incubating with different concentrations of ferulic acid for 30 min at 37°C. Ferulic acid inhibited the activities of α-glucosidase, α-amylase, and pancreatic lipase significantly (p < .05) and promoted glucose uptake in isolated rat psoas muscles. Induction of oxidative pancreatic injury caused significant (p < .05) depletion of glutathione (GSH) level, superoxide dismutase (SOD), and catalase activities, as well as elevation of malondialdehyde (MDA) and nitric oxide (NO) levels, acetylcholinesterase and chymotrypsin activities. Treatment of tissues with ferulic acid significantly (p < .05) reversed these levels and activities. LC-MS analysis of the extracted metabolites revealed 25% depletion of the normal metabolites with concomitant generation of m-Chlorohippuric acid, triglyceride, fructose 1,6-bisphosphate, and ganglioside GM1 in oxidative-injured pancreatic tissues. Treatment with ferulic acid restored uridine diphosphate glucuronic acid and adenosine tetraphosphate and generated P1,P4-Bis(5'-uridyl) tetraphosphate and L-Homocysteic acid, while totally inactivating oxidative-generated metabolites. Ferulic acid also inactivated oxidative-activated pathways, with concomitant reactivation of nucleotide sugars metabolism, starch and sucrose metabolism, and rostenedione metabolism, estrone metabolism, androgen and estrogen metabolism, porphyrin metabolism, and purine metabolism pathways. Taken together, our results indicate the antidiabetic and protective potential of ferulic acid as depicted by its ability to facilitate muscle glucose uptake, inhibit carbohydrate and lipid hydrolyzing enzymes, and modulate oxidative-mediated dysregulated metabolisms. PRACTICAL APPLICATIONS: There have been increasing concerns on the side effects associated with the use of synthetic antidiabetic drug, coupled with their expenses particularly in developing countries. This has necessitated continuous search for alternative treatments especially from natural products having less or no side effects and are readily available. Ferulic acid is among the common phenolics commonly found in fruits and vegetables. In this present study, ferulic acid was able to attenuate oxidative stress, cholinergic dysfunction, and proteolysis in oxidative pancreatic injury, as well as inhibit carbohydrate digesting enzymes. Thus, indicating the ability of the phenolic to protect against complications linked to diabetes. Crops rich in ferulic acid maybe beneficial in managing this disease.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pancreatic Diseases / Oxidative Stress / Coumaric Acids Limits: Animals Language: En Journal: J Food Biochem Year: 2022 Document type: Article Affiliation country: South Africa Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pancreatic Diseases / Oxidative Stress / Coumaric Acids Limits: Animals Language: En Journal: J Food Biochem Year: 2022 Document type: Article Affiliation country: South Africa Country of publication: United States