Urtica dioica Whole Vegetable as a Functional Food Targeting Fat Accumulation and Insulin Resistance-a Preliminary Study in a Mouse Pre-Diabetic Model

Nutrients. 2020 Apr 10;12(4):1059. doi: 10.3390/nu12041059.

Abstract

The shoot of Urtica dioica is used in several cultures as a vegetable or herb. However, not much has been studied about the potential of this plant when consumed as a whole food/vegetable rather than an extract for dietary supplements. In a 12-week dietary intervention study, we tested the effect of U. dioica vegetable on high fat diet induced obesity and insulin resistance in C57BL/6J mice. Mice were fed ad libitum with isocaloric diets containing 10% fat or 45% fat with or without U. dioica. The diet supplemented with U. dioica attenuated high fat diet induced weight gain (p < 0.005; n = 9), fat accumulation in adipose tissue (p < 0.005; n = 9), and whole-body insulin resistance (HOMA-IR index) (p < 0.001; n = 9). Analysis of gene expression in skeletal muscle showed no effect on the constituents of the insulin signaling pathway (AKT, IRS proteins, PI3K, GLUT4, and insulin receptor). Notable genes that impact lipid or glucose metabolism and whose expression was changed by U. dioica include fasting induced adipocyte factor (FIAF) in adipose and skeletal muscle, peroxisome proliferator-activated receptor-α (Ppar-α) and forkhead box protein (FOXO1) in muscle and liver, and Carnitine palmitoyltransferase I (Cpt1) in liver (p < 0.01). We conclude that U. dioica vegetable protects against diet induced obesity through mechanisms involving lipid accumulation and glucose metabolism in skeletal muscle, liver, and adipose tissue.

Keywords: Urtica dioica; diet, fat accumulation; insulin resistance; vegetable.

MeSH terms

  • Adipose Tissue / metabolism*
  • Angiopoietin-Like Protein 4 / metabolism
  • Animals
  • Diet, High-Fat / adverse effects
  • Dietary Supplements*
  • Disease Models, Animal
  • Forkhead Box Protein O1 / genetics
  • Forkhead Box Protein O1 / metabolism
  • Functional Food*
  • Gene Expression
  • Insulin / metabolism
  • Insulin Resistance* / genetics
  • Obesity / diet therapy
  • Obesity / etiology
  • Obesity / genetics
  • Obesity / metabolism
  • PPAR alpha / genetics
  • PPAR alpha / metabolism
  • Prediabetic State / diet therapy*
  • Prediabetic State / etiology
  • Prediabetic State / genetics
  • Prediabetic State / metabolism*
  • Signal Transduction / genetics
  • Urtica dioica*
  • Vegetables*

Substances

  • Angiopoietin-Like Protein 4
  • Angptl4 protein, mouse
  • Forkhead Box Protein O1
  • Foxo1 protein, mouse
  • Insulin
  • PPAR alpha