Effects of essential oil of Satureja khuzestanica on the oxidative stress in experimental hyperthyroid male rat

Authors

  • Fatemeh Zal Reproductive Biology Department, School of Advanced Medical Sciences and Technologies, Shiraz, Iran; Infertility Research Center, Shiraz University of Medical Sciences, Shiraz, Iran
  • Gholam Hossein Ranjbar Omrani Endocrine and Metabolism Research Center, Shiraz University of Medical Sciences, Shiraz, Iran
  • Masood Sepehrimanesh Gastroenterohepatology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran
  • Naser Pajouhi Department of Physiology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran
  • Raheleh Assaei Endocrine and Metabolism Research Center, Shiraz University of Medical Sciences, Shiraz, Iran; Razi Herbal Medicines Research Center, Lorestan University of Medical Sciences, Khorramabad, Iran
  • Zohreh Mostafavi-Pour Maternal-Fetal Medicine Research Center, Shiraz University of Medical Sciences, Shiraz, Iran; Recombinant Protein Laboratory, School of Advanced Medical Sciences and Technologies, Shiraz University of Medical Sciences, Shiraz, Iran
Abstract:

This work analyzes the effects of Satureja khuzestanica essential oil (SKEO) on the thyroid and antioxidant system, assessed by measuring levels of tri-iodothyronine (T3), thyroxine (T4), thyroid-stimulating hormone (TSH), malondialdehyde (MDA), reduced glutathione (GSH), and glutathione peroxidase (GPx) activity. Forty adult male Sprague Dawley rats (225 ± 25 g) were divided into five equal groups: one control and four hyperthyroid groups that received placebo, 200 mg kg-1 body weight of vitamin (Vit.) E, 225 mg kg-1 body weight of SKEO, 200 and 225 mg kg-1 body weight of Vit. E and SKEO together, respectively. Hyperthyroidism was induced by administering of L-thyroxin in drinking water. After 30 days of L-thyroxin consumption, serum T3 and T4 levels, TSH, and oxidative stress indices were determined. Significant increase in serum T3, T4 and MDA concentrations with a simultaneous significant decrease in TSH, GSH level and GPx activity were observed in hyperthyroid group (p <0.05). In the treatment groups, SKEO and/or Vit. E can compensate serum MDA elevation and GPx activity reduction. Only, SKEO + Vit. E could compensate the decline of GSH levels in response to hyperthyroidism. Supplementation of SKEO, plus Vit. E as antioxidants is useful in attenuating lipid peroxidation and may potentially benefit hyperthyroid patients.

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Journal title

volume 6  issue 3

pages  233- 238

publication date 2015-09-01

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