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Co-Administration of Walnut (Juglans Regia) Prevents Systemic Hypertension Induced by Long-Term Use of Dexamethasone: A Promising Strategy for Steroid Consumers Publisher Pubmed



Joukar S1, 2, 3 ; Ebrahimi S3 ; Khazaei M4 ; Bashiri A5 ; Shakibi MR6 ; Naderi V3 ; Shahouzehi B3 ; Alasvand M7
Authors
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Authors Affiliations
  1. 1. Cardiovascular Research Center, Institute of Basic and Clinical Physiology Sciences, Kerman University of Medical Sciences, Kerman, Iran
  2. 2. Department of Physiology and Pharmacology, School of Medicine, Kerman University of Medical Sciences, Kerman, Iran
  3. 3. Physiology Research Center, Kerman University of Medical Sciences, Kerman, Iran
  4. 4. Neurogenic Inflammation Research Center, Department of Physiology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
  5. 5. Faculty of Veterinary Medicine, Shahid Bahonar University of Kerman, Kerman, Iran
  6. 6. Department of Internal Medicine, School of Medicine, Kerman University of Medical Sciences, Kerman, Iran
  7. 7. Department of Physiology, Isfahan University of Medical Sciences, Isfahan, Iran

Source: Pharmaceutical Biology Published:2017


Abstract

Context: The long-term consumption of glucocorticoids (GCs) may induce serious adverse effects such as hypertension. There is sufficient evidence related to the benefit of walnuts on the cardiovascular system. Objective: This study assesses the effect of methanol extract of walnut [Juglans regia L. (Juglandaceae)] on dexamethasone-induced hypertension and the possible mechanisms in Wistar rats. Material and methods: Animals were randomized into control, kernel extract (100 and 200 mg/kg/d, orally), dexamethasone (0.03 mg/kg/d, subcutaneously), dexamethasone + kernel (100 and 200 mg/kg/d, separately), and dexamethasone + captopril (25 mg/kg/d, orally) groups. Animals were treated with water, kernel extract or captopril by gavage 4 d before and during 11 d of saline or dexamethasone treatment. On the 16th day, blood pressure (BP) was recorded and blood samples were collected to measure nitric oxide (NO). Animal hearts were frozen for measurement of malondialdehyde (MDA) and glutathione peroxidase (GPX). Results: Dexamethasone increased the diastolic BP and MDA/GPX ratio in comparison with control group (128 ± 7 vs. 105 ± 3 mmHg, p < 0.05 and 0.2 ± 0.046 vs. 0.08 ± 0.02, p < 0.05). Combination of dexamethasone and walnut (200 mg/kg) prevented the dexamethasone-induced diastolic hypertension (109 ± 3 vs. 128 ± 7 mmHg; p < 0.05), increased the GPX level (14.8 ± 1.46 vs. 5.1 ± 0.64 unit/mg, p < 0.05), reduced the MDA/GPX ratio (0.16 ± 0.015 vs. 0.2 ± 0.046) and improved serum NO level. Conclusion: Similar to captopril, walnut extract normalized dexamethasone-induced hypertension. A part of this beneficial effect apparently involves maintaining balance of the redox system and NO production. © 2016 The Author(s).
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