Zataria multiflora and its constituent, carvacrol, counteract sepsis‐induced aortic and cardiac toxicity in rat: Involvement of nitric oxide and oxidative stress

Author:

Hosseini Mahmoud1ORCID,Arab Zohreh2,Beheshti Farimah34,Anaeigoudari Akbar5,Shakeri Farzaneh67,Rajabian Arezoo8ORCID

Affiliation:

1. Psychiatry and Behavioral Sciences Research Center Mashhad University of Medical Sciences Mashhad Iran

2. Applied Biomedical Research Center Mashhad University of Medical Sciences Mashhad Iran

3. Neuroscience Research Center Torbat Heydariyeh University of Medical Sciences Torbat Heydariyeh Iran

4. Department of Physiology, School of Paramedical Sciences Torbat Heydariyeh University of Medical Sciences Torbat Heydariyeh Iran

5. Department of Physiology, School of Medicine Jiroft University of Medical Sciences Jiroft Iran

6. Natural Products and Medicinal Plants Research Center North Khorasan University of Medical Sciences Bojnurd Iran

7. Department of Physiology and Pharmacology, School of Medicine North Khorasan University of Medical Sciences Bojnurd Iran

8. Department of Internal Medicine, Faculty of Medicine Mashhad University of Medical Sciences Mashhad Iran

Abstract

AbstractBackgroundZataria multiflora and carvacrol showed various pharmacological properties including anti‐inflammatory and anti‐oxidant effects. However, up to now no studies have explored its potential benefits in ameliorating sepsis‐induced aortic and cardiac injury. Thus, this study aimed to investigate the effects of Z. multiflora and carvacrol on nitric oxide (NO) and oxidative stress indicators in lipopolysaccharide (LPS)‐induced aortic and cardiac injury.MethodsAdult male Wistar rats were assigned to: Control, lipopolysaccharide (LPS) (1 mg/kg, intraperitoneal (i.p.)), and Z. multiflora hydro‐ethanolic extract (ZME, 50–200 mg/kg, oral)‐ and carvacrol (25–100 mg/kg, oral)‐treated groups. LPS was injected daily for 14 days. Treatment with ZME and carvacrol started 3 days before LPS administration and treatment continued during LPS administration. At the end of the study, the levels of malondialdehyde (MDA), NO, thiols, and antioxidant enzymes were evaluated.ResultsOur findings showed a significant reduction in the levels of superoxide dismutase (SOD), catalase (CAT), and thiols in the LPS group, which were restored by ZME and carvacrol. Furthermore, ZME and carvacrol decreased MDA and NO in cardiac and aortic tissues of LPS‐injected rats.ConclusionsThe results suggest protective effects of ZME and carvacrol on LPS‐induced cardiovascular injury via improved redox hemostasis and attenuated NO production. However, additional studies are needed to elucidate the effects of ZME and its constituents on inflammatory responses mediated by LPS.

Funder

Mashhad University of Medical Sciences

Publisher

Wiley

Subject

Medical Laboratory Technology,Veterinary (miscellaneous),Molecular Biology,Biochemistry,Medicine (miscellaneous)

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