Paternal obesity and its transgenerational effects on gastrointestinal function in male rat offspring

• Published in: Brazilian journal of medical and biological research Vol. 54; no. 9; p. e11116
• Main Authors: Machado, M P R, Gama, L A, Beckmann, A P S, Hauschildt, A T, Dall'Agnol, D J R, Miranda, J R A, Corá, L A, Américo, M F
• Format: Journal Article
• Language: English; Portuguese
• Published: Brazil Associacao Brasileira de Divulgacao Cientifica (ABDC) 01.01.2021; Revista Brasileira de Pesquisas Medicas; Associação Brasileira de Divulgação Científica
• Subjects: Animals; BIOLOGY; Cecum; Epigenetics; Female; Gastric emptying; Gastrointestinal Motility; Gastrointestinal Transit; Glutamate; Insulin; Intestinal transit; Intestinal transit time; Leptin; Male; MEDICINE, RESEARCH & EXPERIMENTAL; Monosodium glutamate; Morphometry; Obesity; Obesity - etiology; Offspring; Paternal Exposure; Pregnancy; Rats; Rodents; Brazil; Epigenetics; Gastric emptying; Intestinal transit; Monosodium glutamate
• ISSN: 0100-879X; 1414-431X; 1414-431X; 1678-4510
• DOI: 10.1590/1414-431X2020e11116

The interplay between obesity and gastrointestinal (GI) motility is contradictory, and the transgenerational influence on this parameter is unknown. We aimed to evaluate the GI function in a model of paternal obesity and two subsequent generations of their male offspring. Newborn male rats were treated with monosodium glutamate (MSG) and composed the F1 generation, while control rats (CONT) received saline. At 90 days, male F1 were mated with non-obese females to obtain male offspring (F2), which later mated with non-obese females for obtaining male offspring of F3 generation. Lee Index analysis was adopted to set up the obesity groups. Alternating current biosusceptometry (ACB) technique was employed to calculate GI transit parameters: mean gastric emptying time (MGET), mean cecum arrival time (MCAT), mean small intestinal transit time (MSITT), and gastric frequency and amplitude of contractions. Glucose, insulin, and leptin levels and duodenal morphometry were measured. F1 obese rats showed a decrease in the frequency and amplitude of gastric contractions, while obese rats from the F2 generation showed accelerated MGET and delayed MCAT and MSITT. Glucose and leptin levels were increased in F1 and F2 generations. Insulin levels decreased in F1, F2, and F3 generations. Duodenal morphometry was altered in all three generations. Obesity may have paternal transgenerational transmission, and it provoked disturbances in the gastrointestinal function of three generations.