Psychosocial stress increases risk for type 2 diabetes in female cynomolgus macaques consuming a western diet.


Journal

Psychoneuroendocrinology
ISSN: 1873-3360
Titre abrégé: Psychoneuroendocrinology
Pays: England
ID NLM: 7612148

Informations de publication

Date de publication:
05 2022
Historique:
received: 16 10 2021
revised: 23 01 2022
accepted: 25 02 2022
pubmed: 9 3 2022
medline: 6 4 2022
entrez: 8 3 2022
Statut: ppublish

Résumé

Chronic psychosocial stress is associated with increased risk of many chronic diseases including type 2 diabetes mellitus. However, it is difficult to establish a causal relationship between stress and diabetes in human studies because stressors often are self-reported and may be distant in time from metabolic consequences. Macaques are useful models of the effects of chronic psychosocial stress on health and may develop obesity and diabetes similar to human beings. Thus, we studied the relationships between social subordination stress - a well-validated psychological stressor in macaques - and body composition and carbohydrate metabolism in socially housed, middle-aged female cynomolgus monkeys (Macaca fascicularis; n = 42). Following an 8-week baseline phase, the monkeys were fed a Western diet for 36 months (about equivalent to 10 human years). Social status was determined based on the outcomes of agonistic interactions (X¯= 33.3 observation hours/monkey). Phenotypes collected included plasma cortisol, body composition, circulating markers of glucose metabolism, activity levels, and heart rate variability measured as RMSSD (root of mean square of successive differences) and SDDN (standard deviation of beat to beat interval) after 1.5- and 3-years on diet. Mixed model analyses of variance revealed that aggression received, submissions sent, and cortisol were higher, and RMSSD and SDNN were lower in subordinates than dominants (social status: p < 0.05). After 3 years of Western diet consumption, fasting triglyceride, glucose and insulin concentrations, calculated insulin resistance (HOMA-IR), body weight and body fat mass increased in all animals (time: all p's < 0.05); however, the increase in fasting glucose and HOMA-IR was significantly greater in subordinates than dominants (time x social status: p's < 0.05). Impaired glucose metabolism, (glucose > 100 mg/dl) incidence was significantly higher in subordinates (23%) than dominants (0%) (Fisher's exact test, p < 0.05). These findings suggest that chronic psychosocial stress, on a Western diet background, significantly increases type 2 diabetes risk in middle-aged female primates.

Identifiants

pubmed: 35259592
pii: S0306-4530(22)00047-6
doi: 10.1016/j.psyneuen.2022.105706
pmc: PMC8977247
mid: NIHMS1786640
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

105706

Subventions

Organisme : NIA NIH HHS
ID : P30 AG072947
Pays : United States
Organisme : NIMH NIH HHS
ID : R21 MH086731
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG021332
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL087103
Pays : United States
Organisme : NIA NIH HHS
ID : T32 AG033534
Pays : United States
Organisme : NIH HHS
ID : T32 OD010957
Pays : United States

Informations de copyright

Copyright © 2022 Elsevier Ltd. All rights reserved.

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Auteurs

Marnie G Silverstein-Metzler (MG)

Department of Pathology/Comparative Medicine, Wake Forest School of Medicine, USA.

Brett M Frye (BM)

Department of Pathology/Comparative Medicine, Wake Forest School of Medicine, USA.

Jamie N Justice (JN)

Internal Medicine/Gerontology and Geriatric Medicine, Wake Forest School of Medicine, USA.

Thomas B Clarkson (TB)

Department of Pathology/Comparative Medicine, Wake Forest School of Medicine, USA.

Susan E Appt (SE)

Department of Pathology/Comparative Medicine, Wake Forest School of Medicine, USA.

J Jeffrey Carr (J)

Department of Radiology and Radiological Sciences, Vanderbilt University School of Medicine, USA.

Thomas C Register (TC)

Department of Pathology/Comparative Medicine, Wake Forest School of Medicine, USA.

Mays Albu-Shamah (M)

Department of Pathology/Comparative Medicine, Wake Forest School of Medicine, USA.

Hossam A Shaltout (HA)

Department of Obstetrics and Gynecology, Wake Forest School of Medicine, USA.

Carol A Shively (CA)

Department of Pathology/Comparative Medicine, Wake Forest School of Medicine, USA. Electronic address: cshively@wakehealth.edu.

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