Absence of MyD88 from Skeletal Muscle Protects Female Mice from Inactivity‐Induced Adiposity and Insulin Resistance

Objective Inactivity and inflammation are linked to obesity and insulin resistance. It was hypothesized that MyD88 (mediates inflammation) knockout from muscle (MusMyD88−/−) would prevent, whereas miR146a−/− (MyD88 inhibitor) would exacerbate, inactivity‐induced metabolic disturbances. Methods Cre‐c...

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Published in:Obesity (Silver Spring, Md.) Md.), 2020-04, Vol.28 (4), p.772-782
Main Authors: Mahmassani, Ziad S., Reidy, Paul T., McKenzie, Alec I., Petrocelli, Jonathan J., Matthews, O’Connor, Hart, Naomi M., Ferrara, Patrick J., O’Connell, Ryan M., Funai, Katsuhiko, Drummond, Micah J.
Format: Article
Language:English
Subjects:
Adiposity - genetics
Animals
Body composition
Disease Models, Animal
Energy consumption
Fatty acids
Female
Females
Food
Glucose
Histology
Inflammation
Insulin resistance
Insulin Resistance - physiology
Laboratories
Metabolism
Mice
Mice, Inbred C57BL
Muscle, Skeletal - metabolism
Musculoskeletal system
Myeloid Differentiation Factor 88 - metabolism
NMR
Nuclear magnetic resonance
Obesity
Obesity - metabolism
Proteins
Respiration
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Summary:Objective Inactivity and inflammation are linked to obesity and insulin resistance. It was hypothesized that MyD88 (mediates inflammation) knockout from muscle (MusMyD88−/−) would prevent, whereas miR146a−/− (MyD88 inhibitor) would exacerbate, inactivity‐induced metabolic disturbances. Methods Cre‐control, MusMyD88−/−, and miR146a−/− mice were given running wheels for 5 weeks to model an active phenotype. Afterward, half were placed into a small mouse cage (SMC) to restrict movement for 8 days. Body composition, muscle (3H)2‐deoxyglucose uptake, visceral fat histology, and tissue weight (hind limb muscles, visceral fat, and liver) were assessed. In skeletal muscle and visceral fat, RNA sequencing and mitochondrial function were performed on female MusMyD88−/− and Cre‐control SMC mice. Results The SMC induced adiposity, hyperinsulinemia, and muscle insulin‐stimulated glucose uptake, which was worsened in miR146a−/− mice. In females, MusMyD88−/− mice were protected. Female MusMyD88−/− mice during the SMC period (vs. Cre‐control) exhibited higher Igf1 and decreased Ip6k3 and Trim63 muscle expression. Visceral fat transcript changes corresponded to improved lipid metabolism, decreased adipose expansion (Gulp1↑, Anxa2↓, Ehd1↓) and meta‐inflammation (Hmox1↓), and increased beiging (Fgf10↑). Ralgapa2, negative regulator of GLUT4 translocation, and inflammation‐related gene 993011J21Rik2 were decreased in both muscle and fat. Conclusions Whole‐body miR146a−/− exacerbated inactivity‐induced fat gain and muscle insulin resistance, whereas MusMyD88−/− prevented insulin resistance in female mice.
ISSN:1930-7381
1930-739X
DOI:10.1002/oby.22759