Literature DB >> 11054596

Metabolic imprinting on genetically predisposed neural circuits perpetuates obesity.

B E Levin1.   

Abstract

There is an obesity epidemic in the industrialized world that is not simply explained by excess energy intake and decreased energy expenditure. Persistent obesity develops when genetically predisposed individuals are in a chronic state of positive energy balance. Once established, the obese body weight is avidly defended against both over- and underfeeding. Animal studies have shown that lean individuals who are genetically predisposed toward obesity have abnormalities of neural function that prime them to become obese when caloric density of the diet is raised. These neural abnormalities are gradually "corrected" as obesity becomes fully developed, suggesting that obesity is the normal state for such individuals. Thus, defense of the obese body weight may be perpetuated by the formation of new neural circuits involved in energy-homeostasis pathways that are not then easily abolished. Such neural plasticity can occur in both adult life and during nervous-system development. Early pre- and postnatal metabolic conditions (maternal diabetes, obesity, undernutrition) can lead genetically predisposed offspring to become even more obese as adults. This enhanced obesity is associated with altered brain neural circuitry, and these changes can then be passed on to subsequent generations in a feed-forward cycle of ever-increasing body weight. Thus, the metabolic perturbations associated with obesity during both brain development and adult life can produce "metabolic imprinting" on genetically predisposed neural circuits involved in energy homeostasis. Drugs that reduce body weight decrease the defended body weight and alter neural pathways involved in energy homeostasis but have no permanent effect on body weight or neural function in most individuals. Thus, early intervention in mothers, infants, children, and adults may be the only way to prevent the formation of permanent neural connections that promote and perpetuate obesity in genetically predisposed individuals.

Entities:  

Mesh:

Year:  2000        PMID: 11054596     DOI: 10.1016/s0899-9007(00)00408-1

Source DB:  PubMed          Journal:  Nutrition        ISSN: 0899-9007            Impact factor:   4.008


  15 in total

1.  Changes in melanocortin expression and inflammatory pathways in fetal offspring of nonhuman primates fed a high-fat diet.

Authors:  B E Grayson; P R Levasseur; S M Williams; M S Smith; D L Marks; K L Grove
Journal:  Endocrinology       Date:  2010-02-22       Impact factor: 4.736

Review 2.  Relevance of animal models to human eating disorders and obesity.

Authors:  Regina C Casper; Elinor L Sullivan; Laurence Tecott
Journal:  Psychopharmacology (Berl)       Date:  2008-03-04       Impact factor: 4.530

Review 3.  Metabolic imprinting: critical impact of the perinatal environment on the regulation of energy homeostasis.

Authors:  Barry E Levin
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2006-07-29       Impact factor: 6.237

Review 4.  Perinatal environment and its influences on metabolic programming of offspring.

Authors:  Kellie L K Tamashiro; Timothy H Moran
Journal:  Physiol Behav       Date:  2010-04-13

Review 5.  Developmental gene x environment interactions affecting systems regulating energy homeostasis and obesity.

Authors:  Barry E Levin
Journal:  Front Neuroendocrinol       Date:  2010-03-03       Impact factor: 8.606

6.  Impairment of acquisition of cocaine self-administration in rats maintained on a high-fat diet.

Authors:  Paul J Wellman; Jack R Nation; Kristina W Davis
Journal:  Pharmacol Biochem Behav       Date:  2007-07-21       Impact factor: 3.533

Review 7.  Stress exposure, food intake and emotional state.

Authors:  Yvonne M Ulrich-Lai; Stephanie Fulton; Mark Wilson; Gorica Petrovich; Linda Rinaman
Journal:  Stress       Date:  2015-08-13       Impact factor: 3.493

8.  Effects of Chronic Social Stress on Obesity.

Authors:  Karen A Scott; Susan J Melhorn; Randall R Sakai
Journal:  Curr Obes Rep       Date:  2012-03

Review 9.  Gene-environment interactions controlling energy and glucose homeostasis and the developmental origins of obesity.

Authors:  Sebastien Bouret; Barry E Levin; Susan E Ozanne
Journal:  Physiol Rev       Date:  2015-01       Impact factor: 37.312

10.  Prenatal stress or high-fat diet increases susceptibility to diet-induced obesity in rat offspring.

Authors:  Kellie L K Tamashiro; Chantelle E Terrillion; Jayson Hyun; James I Koenig; Timothy H Moran
Journal:  Diabetes       Date:  2009-02-02       Impact factor: 9.461

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.