Title: Consensus on the key characteristics of metabolism disruptors |
Authors: La Merrill, Michele A. Smith, Martyn T. McHale, Cliona M. Heindel, Jerrold J. Atlas, Ella Cave, Matthew C. Collier, David Guyton, Kathryn Z. Koliwad, Suneil Nadal, Ángel Rhoder, Christopher J. Sargis, Robert M. Zeise, Lauren Blumberg, Bruce |
Editor: Nature Research |
Department: Departamentos de la UMH::Fisiología |
Issue Date: 2024-11 |
URI: https://hdl.handle.net/11000/37999 |
Abstract:
Metabolism-disrupting agents (MDAs) are chemical, infectious
or physical agents that increase the risk of metabolic disorders.
Examples include pharmaceuticals, such as antidepressants, and
environmental agents, such as bisphenol A. Various types of studies
can provide evidence to identify MDAs, yet a systematic method
is needed to integrate these data to help to identify such hazards.
Inspired by work to improve hazard identification of carcinogens
using key characteristics (KCs), we developed 12 KCs of MDAs based
on our knowledge of processes underlying metabolic diseases and
the effects of their causal agents: (1) alters function of the endocrine
pancreas; (2) impairs function of adipose tissue; (3) alters nervous
system control of metabolic function; (4) promotes insulin resistance;
(5) disrupts metabolic signalling pathways; (6) alters development and
fate of metabolic cell types; (7) alters energy homeostasis; (8) causes
inappropriate nutrient handling and partitioning; (9) promotes
chronic inflammation and immune dysregulation in metabolic tissues;
(10) disrupts gastrointestinal tract function; (11) induces cellular stress
pathways; and (12) disrupts circadian rhythms. In this Consensus
Statement, we present the logic that revealed the KCs of MDAs and
highlight evidence that supports the identification of KCs. We use
chemical, infectious and physical agents as examples to illustrate how
the KCs can be used to organize and use mechanistic data to help to
identify MDAs.
|
Keywords/Subjects: Dyslipidaemias Metabolic syndrome Obesity Risk factors Type 2 diabetes |
Type of document: info:eu-repo/semantics/article |
Access rights: info:eu-repo/semantics/closedAccess Attribution-NonCommercial-NoDerivatives 4.0 Internacional |
DOI: https://doi.org/10.1038/s41574-024-01059-8 |
Published in: Nature Reviews Endocrinology, Vol. 21 (2025) |
Appears in Collections: Artículos Fisiología
|