Hypoglycemic and hypolipidemic effects of Lippia origanoides Kunth in diabetic rats

Author:

Miranda Vinicius Carvalho1,Pereira Yago Luis Gonçalves1ORCID,da Paz Allane Patricia Santos1ORCID,de Souza Keyla Rodrigues1ORCID,da Silva Márcia Cristina Freitas2ORCID,Muto Nilton Akio3ORCID,Monteiro Patrick Romano4ORCID,Santos Agenor Valadares4ORCID,Hamoy Moises5ORCID,de Medeiros Maria das Graças Freire6ORCID,do Carmo Iolanda Souza7ORCID,Silva Maria Eduarda Moraes7,de Sousa Lima Neto José8ORCID,de Mello Vanessa Jóia1ORCID

Affiliation:

1. Research, Teaching and Extension Laboratory in Clinical Analysis, Institute of Biological Sciences Federal University of Pará Belém Brazil

2. Human and Environmental Toxicology, Tropical Medicine Nucleus Federal University of Pará Belém Brazil

3. Center for the Valorization of Bioactive Compounds from the Amazon Federal University of Pará Belém Brazil

4. Laboratory of Biotechnology of Enzymes and Biotransformation Federal University of Pará Belém Brazil

5. Laboratory of Pharmacology and Toxicology of Natural Products, Institute of Biological Sciences Federal University of Pará Belém Brazil

6. Laboratory of Technological Innovation and Entrepreneurship in Drug–LITE Federal University of Piauí Teresina Brazil

7. Laboratory of Organic Geochemistry–LAGO Federal University of Piauí Teresina Brazil

8. Department of Biology, Center for Biological and Health Sciences Federal University of Maranhão São Luís Brazil

Abstract

AbstractDiabetes mellitus is a metabolic disorder commonly associated with atherosclerosis. Plants with therapeutic potential, such as Lippia origanoides Kunth, emerge as effective alternatives for treating these diseases. Therefore, this work aims to analyze the antihyperglycemic and antidyslipidemic potential of the hydroalcoholic extract of Lippia origanoides Kunth (ELo) in alloxan‐diabetic rats. Animals were treated orally: normal control, hyperglycemic control, positive control glibenclamide (5 mg/kg), and groups treated with ELo (75, 150, and 250 mg/kg). Preclinical evaluation of ELo showed hypoglycemic, hypolipidemic, hepatic, and renal protective effects. At all doses, ELo significantly reduced hyperglycemia, triglycerides, total cholesterol, low‐density lipoprotein, atherogenic index, atherogenic coefficient, and cardiovascular risk index (p < .05). Elo at different doses promoted an increase in insulin release compared to untreated animals (p < .05) and showed α‐glucosidase inhibitory activity (p < .05). Also, ELo (250 mg/kg group) showed maximum reduction of hyperglycemia, alanine transaminase, aspartate aminotransferase, malonaldehyde, and urea compared to the hyperglycemic and glibenclamide groups, and creatinine only compared to the hyperglycemic groups (p < .05). The promising action of ELo in the context of diabetes may be related to the synergistic action of flavonoid compounds identified in liquid chromatography, whose pharmacological capabilities have already been documented in previous studies. The mechanisms may be the stimulation of insulin release; the inhibitory activity of α‐glucosidase; improving general clinical conditions; and the antioxidant effects of the extract. These findings pave the way for the future development of an herbal presentation of L. origanoides Kunth as a hypoglycemic and cardiovascular protector with a lipid‐lowering effect.

Publisher

Wiley

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