Improved Sp1 and Betaine Homocysteine-S-Methyltransferase Expression and Homocysteine Clearance Are Involved in the Effects of Zinc on Oxidative Stress in High-Fat-Diet-Pretreated Mice

Biol Trace Elem Res. 2018 Aug;184(2):436-441. doi: 10.1007/s12011-017-1214-9. Epub 2017 Dec 4.

Abstract

Zinc plays a role in alleviating oxidative stress. However, the related mechanisms remain to be further elucidated. The present study was conducted to investigate whether the recovery of oxidative stress in high-fat-diet (HFD)-pretreated mice was affected by zinc. Male mice received either an HFD or a low-fat-diet (LFD) for 8 weeks. Then, the mice fed with HFD and LFD were both assigned to either a control diet (30 mg zinc, ZD) or a no-added zinc diet (NZD) for an additional 4 weeks. The results showed that after feeding with NZD for 4 weeks, the HFD-pretreated mice had the highest plasma glucose and insulin concentrations, while had the lowest CuZn-SOD and glutathione concentrations. Moreover, after feeding with NZD for 4 weeks, the HFD-pretreated mice had the highest hepatic ROS and homocysteine concentrations, while had the lowest glutathione and methionine concentrations. Furthermore, the HFD-pretreated mice fed with NZD for 4 weeks had the lowest gene and protein expression of betaine homocysteine-S-methyltransferase (BHMT), cystathionine β-synthase, and Sp1. The results suggested that zinc was critical for oxidative stress alleviation and homocysteine clearance in HFD-pretreated mice. It was further elucidated that improved Sp1 and BHMT expression are involved in the effects of zinc on oxidative stress.

Keywords: Betaine homocysteine-S-methyltransferase; Cystathionine β-synthase; Homocysteine; Sp1; Zinc.

MeSH terms

  • Animals
  • Betaine-Homocysteine S-Methyltransferase / genetics*
  • Betaine-Homocysteine S-Methyltransferase / metabolism
  • Blood Glucose / metabolism
  • Diet, High-Fat*
  • Gene Expression / drug effects
  • Glutathione / metabolism
  • Homocysteine / metabolism*
  • Insulin / blood
  • Liver / drug effects
  • Liver / metabolism
  • Male
  • Mice, Inbred C57BL
  • Oxidative Stress / drug effects*
  • Reactive Oxygen Species / metabolism
  • Sp1 Transcription Factor / genetics*
  • Sp1 Transcription Factor / metabolism
  • Superoxide Dismutase-1
  • Zinc / administration & dosage
  • Zinc / pharmacology*

Substances

  • Blood Glucose
  • Insulin
  • Reactive Oxygen Species
  • Sp1 Transcription Factor
  • Homocysteine
  • Superoxide Dismutase-1
  • Betaine-Homocysteine S-Methyltransferase
  • Bhmt protein, mouse
  • Glutathione
  • Zinc