Maternal periodontitis potentiates monosodium glutamate-obesity damage on Wistar offspring's fast-glycolytic muscle

Oral Dis. 2024 Oct;30(7):4705-4720. doi: 10.1111/odi.14890. Epub 2024 Feb 5.

Abstract

Objective: To evaluate the effects of magnifying the damage caused by obesity induced by monosodium glutamate, using a model of maternal periodontitis, on the structure of the anterior tibialis muscle of the offspring.

Materials and methods: Twenty-four female Wistar rats were divided into four experimental groups: control (n = 6), obese (n = 6), control with periodontitis (n = 6) and obese with periodontitis (n = 6). At 78 days of life, the rats were mated with males without any experimental intervention. The offspring of these rats (n = 1/L), at 120 days of life, were weighed and measured, then euthanized. Plasma was collected for analysis of cytokines IL-6, IL-10, IL-17 and TNF-α. Adipose tissues were collected and weighed, and the anterior tibial muscle was designated for histomorphological analyses (n = 6/group).

Results: Monosodium glutamate offspring showed significant muscle changes, such as a reduction in the size of fibres and neuromuscular junctions, and an increase in the nucleus and capillaries. However, all these changes were more expressed in monosodium glutamate-obese with periodontitis offspring.

Conclusion: This leads us to suggest a magnifying effect promoted by periodontitis to the damage already well described by monosodium glutamate-obesity, determined by low-intensity inflammation, causing greater muscle damage.

Keywords: chronic inflammatory diseases; foetal programming; histological alterations; tibialis anterior.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cytokines / metabolism
  • Female
  • Male
  • Muscle, Skeletal* / pathology
  • Obesity* / complications
  • Obesity* / metabolism
  • Periodontitis* / complications
  • Periodontitis* / metabolism
  • Periodontitis* / pathology
  • Pregnancy
  • Prenatal Exposure Delayed Effects
  • Rats
  • Rats, Wistar*
  • Sodium Glutamate* / adverse effects
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Sodium Glutamate
  • Tumor Necrosis Factor-alpha
  • Cytokines