2023
DOI: 10.1016/j.bcp.2022.115407
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Chronic kidney disease-induced muscle atrophy: Molecular mechanisms and promising therapies

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Cited by 21 publications
(23 citation statements)
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“…Numerous studies have focused on the mechanisms underlying CKD, with scar formationmediated progressive renal injury recognized as a common pathogenic pathway responsible for its development. [6][7][8] The pathological hallmark of CKD involves the accumulation of a substantial amount of extracellular matrix in the glomerulus and renal interstitium, which disrupts normal renal tissue architecture and interacts with renal tubular epithelial cells, myofibroblasts, and immune cells, further exacerbating the progression to renal fibrosis and nephron loss. [9,10] Dysbiosis of the gut microbiota has been implicated in the development of various diseases.…”
Section: Bibliometric Analysis Of the Relationship Between Gut Microb...mentioning
confidence: 99%
“…Numerous studies have focused on the mechanisms underlying CKD, with scar formationmediated progressive renal injury recognized as a common pathogenic pathway responsible for its development. [6][7][8] The pathological hallmark of CKD involves the accumulation of a substantial amount of extracellular matrix in the glomerulus and renal interstitium, which disrupts normal renal tissue architecture and interacts with renal tubular epithelial cells, myofibroblasts, and immune cells, further exacerbating the progression to renal fibrosis and nephron loss. [9,10] Dysbiosis of the gut microbiota has been implicated in the development of various diseases.…”
Section: Bibliometric Analysis Of the Relationship Between Gut Microb...mentioning
confidence: 99%
“…By activating the UPS and blocking the IGF-1/phosphatidylinositol-3 kinase (PI3K)/protein kinase B (AKT) signaling pathways, metabolic acidosis speeds up muscle atrophy [ 101 ]. While IGF-1/PI3K/AKT functions as the most significant anabolic pathway in muscle tissue, the UPS is the primary regulatory mechanism for protein breakdown in skeletal muscle [ 101 ]. Additionally, activation of AKT also inhibits protein degradation in skeletal muscle by stimulating the phosphorylation and inactivation of FOXO transcription factors.…”
Section: Recommended Approach and Potential Treatments For Ckd-associ...mentioning
confidence: 99%
“…Additionally, activation of AKT also inhibits protein degradation in skeletal muscle by stimulating the phosphorylation and inactivation of FOXO transcription factors. As a result, metabolic acidosis simultaneously stimulates protein breakdown and inhibits protein synthesis, as well as causing oxidative stress and inflammation in muscle tissue [ 101 ].…”
Section: Recommended Approach and Potential Treatments For Ckd-associ...mentioning
confidence: 99%
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“…For example, patients with CKD and ESKD often present with peripheral neuropathy 10 , which can cause motor dysfunction. The common complications of CKD include anemia, cardiovascular disease, decreased red blood cell survival, iron deficiency, malnutrition, muscle weakness, and osteoporosis due to disturbances in calcium, vitamin D, and phosphate metabolism 4, 11 . Both anemia and malnutrition can directly contribute to muscle dysfunction 11, 12 .…”
Section: Introductionmentioning
confidence: 99%