Rice Bran Protein Hydrolysates Improve Insulin Resistance and Decrease Pro-inflammatory Cytokine Gene Expression in Rats Fed a High Carbohydrate-High Fat Diet

Nutrients. 2015 Aug 3;7(8):6313-29. doi: 10.3390/nu7085292.

Abstract

A high carbohydrate-high fat (HCHF) diet causes insulin resistance (IR) and metabolic syndrome (MS). Rice bran has been demonstrated to have anti-dyslipidemic and anti-atherogenic properties in an obese mouse model. In the present study, we investigated the beneficial effects of rice bran protein hydrolysates (RBP) in HCHF-induced MS rats. After 12 weeks on this diet, the HCHF-fed group was divided into four subgroups, which were orally administered RBP 100 or 500 mg/kg, pioglitazone 10 mg/kg, or tap water for a further 6 weeks. Compared with normal diet control group, the MS rats had elevated levels of blood glucose, lipid, insulin, and HOMA-IR. Treatment with RBP significantly alleviated all those changes and restored insulin sensitivity. Additionally, RBP treatment increased adiponectin and suppressed leptin levels. Expression of Ppar-γ mRNA in adipose tissues was significantly increased whereas expression of lipogenic genes Srebf1 and Fasn was significantly decreased. Levels of mRNA of proinflammatory cytokines, Il-6, Tnf-α, Nos-2 and Mcp-1 were significantly decreased. In conclusion, the present findings support the consumption of RBP as a functional food to improve insulin resistance and to prevent the development of metabolic syndrome.

Keywords: inflammatory cytokines; insulin resistance; metabolic syndrome; rice bran protein hydrolysates (RBP).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipokines / blood
  • Adipose Tissue / metabolism
  • Animals
  • Cytokines / genetics
  • Cytokines / metabolism*
  • Diet* / adverse effects
  • Dietary Carbohydrates / administration & dosage
  • Dietary Carbohydrates / adverse effects
  • Dietary Fats / administration & dosage
  • Dietary Fats / adverse effects
  • Edible Grain / chemistry
  • Functional Food
  • Gene Expression / drug effects
  • Inflammation Mediators / blood
  • Inflammation* / genetics
  • Inflammation* / metabolism
  • Inflammation* / prevention & control
  • Insulin / blood
  • Insulin Resistance*
  • Lipogenesis / drug effects
  • Lipogenesis / genetics
  • Male
  • Metabolic Syndrome / blood
  • Metabolic Syndrome / drug therapy*
  • Metabolic Syndrome / etiology
  • Oryza / chemistry*
  • PPAR gamma / genetics
  • PPAR gamma / metabolism
  • Protein Hydrolysates / pharmacology*
  • Protein Hydrolysates / therapeutic use
  • Rats, Sprague-Dawley

Substances

  • Adipokines
  • Cytokines
  • Dietary Carbohydrates
  • Dietary Fats
  • Inflammation Mediators
  • Insulin
  • PPAR gamma
  • Protein Hydrolysates