Organ Crosstalk Contributes to Muscle Wasting in Chronic Kidney Disease

被引:4
作者
Wang, Xiaonan H. [1 ]
Price, S. Russ [2 ,3 ,4 ]
机构
[1] Emory Univ, Dept Med, Renal Div, Atlanta, GA 30322 USA
[2] East Carolina Univ, Brody Sch Med, Dept Biochem & Mol Biol, Greenville, NC USA
[3] East Carolina Univ, Brody Sch Med, Dept Internal Med, Greenville, NC USA
[4] East Carolina Univ, Brody Sch Med, Dept Biochem & Mol Biol, 600 Moye Blvd,Room 4N-84, Greenville, NC 27834 USA
关键词
Chronic kidney disease; skeletal muscle; protein-energy wasting; muscle atrophy; crosstalk; STAGE RENAL-DISEASE; SKELETAL-MUSCLE; PROTEIN-SYNTHESIS; AEROBIC EXERCISE; INTERNATIONAL SOCIETY; METABOLIC-ACIDOSIS; INSULIN-RESISTANCE; ENCODING PROTEINS; PHYSICAL-ACTIVITY; MESSENGER-RNAS;
D O I
10.1016/j.semnephrol.2023.151409
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Muscle wasting (ie, atrophy) is a serious consequence of chronic kidney disease (CKD) that reduces muscle strength and function. It reduces the quality of life for CKD patients and increases the risks of comorbidities and mortality. Current treatment strategies to prevent or reverse skeletal muscle loss are limited owing to the broad and systemic nature of the initiating signals and the multifaceted catabolic mechanisms that accelerate muscle protein degradation and impair protein synthesis and repair pathways. Recent evidence has shown how organs such as muscle, adipose, and kidney communicate with each other through interorgan exchange of proteins and RNAs during CKD. This crosstalk changes cell functions in the recipient organs and represents an added dimension in the complex processes that are responsible for muscle atrophy in CKD. This complexity creates challenges for the development of effective therapies to ameliorate muscle wasting and weakness in patients
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页数:17
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共 135 条
  • [61] Aerobic exercise in obese diabetic patients with chronic kidney disease: a randomized and controlled pilot study
    Leehey, David J.
    Moinuddin, Irfan
    Bast, Joseph P.
    Qureshi, Shahzad
    Jelinek, Christine S.
    Cooper, Cheryl
    Edwards, Lonnie C.
    Smith, Bridget M.
    Collins, Eileen G.
    [J]. CARDIOVASCULAR DIABETOLOGY, 2009, 8
  • [62] Global kidney health 2017 and beyond: a roadmap for closing gaps in care, research, and policy
    Levin, Adeera
    Tonelli, Marcello
    Bonventre, Joseph
    Coresh, Josef
    Donner, Jo-Ann
    Fogo, Agnes B.
    Fox, Caroline S.
    Gansevoort, Ron T.
    Heerspink, Hiddo J. L.
    Jardine, Meg
    Kasiske, Bertram
    Koettgen, Anna
    Kretzler, Matthias
    Levey, Andrew S.
    Luyckx, Valerie A.
    Mehta, Ravindra
    Moe, Orson
    Obrador, Gregorio
    Pannu, Neesh
    Parikh, Chirag R.
    Perkovic, Vlado
    Pollock, Carol
    Stenvinkel, Peter
    Tuttle, Katherine R.
    Wheeler, David C.
    Eckardt, Kai-Uwe
    [J]. LANCET, 2017, 390 (10105) : 1888 - 1917
  • [63] Atrogin-1/rnuscle atrophy F-box inhibits calcineurin-dependent cardiac hypertrophy by participating in an SCF ubiquitin ligase complex
    Li, HH
    Kedar, V
    Zhang, CL
    McDonough, H
    Arya, R
    Wang, DZ
    Patterson, C
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2004, 114 (08) : 1058 - 1071
  • [64] mTOR at the nexus of nutrition, growth, ageing and disease
    Liu, Grace Y.
    Sabatini, David M.
    [J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2020, 21 (04) : 183 - 203
  • [65] Impacts of Indoxyl Sulfate and p-Cresol Sulfate on Chronic Kidney Disease and Mitigating Effects of AST-120
    Liu, Wen-Chih
    Tomino, Yasuhiko
    Lu, Kuo-Cheng
    [J]. TOXINS, 2018, 10 (09)
  • [66] Identification of atrogin-1-targeted proteins during the myostatin-induced skeletal muscle wasting
    Lokireddy, Sudarsanareddy
    Wijesoma, Isuru Wijerupage
    Sze, Siu Kwan
    McFarlane, Craig
    Kambadur, Ravi
    Sharma, Mridula
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2012, 303 (05): : C512 - C529
  • [67] DEATH RISK IN HEMODIALYSIS-PATIENTS - THE PREDICTIVE VALUE OF COMMONLY MEASURED VARIABLES AND AN EVALUATION OF DEATH RATE DIFFERENCES BETWEEN FACILITIES
    LOWRIE, EG
    LEW, NL
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 1990, 15 (05) : 458 - 482
  • [68] EFFECTS OF AMMONIUM CHLORIDE ACIDOSIS ON THE ACTION OF INSULIN IN DOGS
    MACKLER, B
    LICHTENSTEIN, H
    GUEST, GM
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1951, 166 (01): : 191 - 198
  • [69] Mechanisms of Disease: cytokine and adipokine signaling in uremic cachexia
    Mak, Robert H.
    Cheung, Wai
    Cone, Roger D.
    Marks, Daniel L.
    [J]. NATURE CLINICAL PRACTICE NEPHROLOGY, 2006, 2 (09): : 527 - 534
  • [70] Ubiquitin (UbC) expression in muscle cells is increased by glucocorticoids through a mechanism involving Sp1 and MEK1
    Marinovic, AC
    Zheng, B
    Mitch, WE
    Price, SR
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (19) : 16673 - 16681