4.7 Article

The role of IL-1 in adipose browning and muscle wasting in CKD-associated cachexia

Journal

SCIENTIFIC REPORTS
Volume 11, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41598-021-94565-y

Keywords

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Funding

  1. NIH [R01HD095547, U01DK066143, RO1DK125811, R01DK113592, R01HL140898, R01AI134030]
  2. California Institute of Regenerative Medicine [CLIN2-11478]
  3. Cystinosis Research Foundation
  4. UC collaborative grant
  5. Spring Sunlight Program cooperative research project of Ministry of education [HLJ2019023]
  6. Research Fund for Young & Middle-Aged Innovative Science of the Second Affiliated Hospital of Harbin Medical University [CX2016-03]

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By studying the effects of cytokines on cachexia in chronic kidney disease, it was found that IL-1 receptor antagonism may represent a novel targeted treatment for adipose tissue browning and muscle wasting in CKD.
Cytokines such as IL-6, TNF-alpha and IL-1 beta trigger inflammatory cascades which may play a role in the pathogenesis of chronic kidney disease (CKD)-associated cachexia. CKD was induced by 5/6 nephrectomy in mice. We studied energy homeostasis in Il1 beta (-/-)/CKD, Il6(-/-)/CKD and Tnf alpha (-/-)/CKD mice and compared with wild type (WT)/CKD controls. Parameters of cachexia phenotype were completely normalized in Il1 beta (-/-)/CKD mice but were only partially rescued in Il6(-/-)/CKD and Tnf alpha (-/-)/CKD mice. We tested the effects of anakinra, an IL-1 receptor antagonist, on CKD-associated cachexia. WT/CKD mice were treated with anakinra (2.5 mg/kg/day, IP) or saline for 6 weeks and compared with WT/Sham controls. Anakinra normalized food intake and weight gain, fat and lean mass content, metabolic rate and muscle function, and also attenuated molecular perturbations of energy homeostasis in adipose tissue and muscle in WT/CKD mice. Anakinra decreased serum and muscle expression of IL-6, TNF-alpha and IL-1 beta in WT/CKD mice. Anakinra attenuated browning of white adipose tissue in WT/CKD mice. Moreover, anakinra normalized gastrocnemius weight and fiber size as well as attenuated muscle fat infiltration in WT/CKD mice. This was accompanied by correcting the increased muscle wasting signaling pathways while promoting the decreased myogenesis process in gastrocnemius of WT/CKD mice. We performed qPCR analysis for the top 20 differentially expressed muscle genes previously identified via RNAseq analysis in WT/CKD mice versus controls. Importantly, 17 differentially expressed muscle genes were attenuated in anakinra treated WT/CKD mice. In conclusion, IL-1 receptor antagonism may represent a novel targeted treatment for adipose tissue browning and muscle wasting in CKD.

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