Low-Dose Coconut Oil Supplementation Induces Hypothalamic Inflammation, Behavioral Dysfunction, and Metabolic Damage in Healthy Mice

Mol Nutr Food Res. 2021 May;65(10):e2000943. doi: 10.1002/mnfr.202000943. Epub 2021 Apr 17.

Abstract

Scope: Coconut oil (CO) diets remain controversial due to the possible association with metabolic disorder and obesity. This study investigates the metabolic effects of a low amount of CO supplementation.

Methods and results: Swiss male mice are assigned to be supplemented orally during 8 weeks with 300 µL of water for the control group (CV), 100 or 300 µL of CO (CO100 and CO300) and 100 or 300 µL of soybean oil (SO; SO100 and SO300). CO led to anxious behavior, increase in body weight gain, and adiposity. In the hypothalamus, CO and SO increase cytokines expression and pJNK, pNFKB, and TLR4 levels. Nevertheless, the adipose tissue presented increases macrophage infiltration, TNF-α and IL-6 after CO and SO consumption. IL-1B and CCL2 expression, pJNK and pNFKB levels increase only in CO300. In the hepatic tissue, CO increases TNF-α and chemokines expression. Neuronal cell line (mHypoA-2/29) exposed to serum from CO and SO mice shows increased NFKB migration to the nucleus, TNF-α, and NFKBia expression, but are prevented by inhibitor of TLR4 (TAK-242).

Conclusions: These results show that a low-dose CO changes the behavioral pattern, induces inflammatory pathway activation, TLR4 expression in healthy mice, and stimulates the pro-inflammatory response through a TLR4-mediated mechanism.

Keywords: adipose tissue; coconut oil; hypothalamus; inflammation; metabolic parameters.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adiposity / drug effects
  • Animals
  • Behavior, Animal / drug effects*
  • Blood Glucose / analysis
  • Coconut Oil / administration & dosage*
  • Coconut Oil / adverse effects*
  • Dietary Supplements
  • Hypothalamic Diseases / chemically induced*
  • Inflammation / chemically induced*
  • Male
  • Metabolic Diseases / chemically induced*
  • Mice
  • Motor Activity / drug effects
  • Toll-Like Receptor 4 / antagonists & inhibitors
  • Toll-Like Receptor 4 / physiology
  • Weight Gain / drug effects

Substances

  • Blood Glucose
  • Tlr4 protein, mouse
  • Toll-Like Receptor 4
  • Coconut Oil