Hypophosphatemia promotes lower rates of muscle ATP synthesis

被引:73
作者
Pesta, Dominik H. [1 ]
Tsirigotis, Dimitrios N. [2 ]
Befroy, Douglas E. [3 ]
Caballero, Daniel [1 ]
Jurczak, Michael J. [1 ]
Rahimi, Yasmeen [1 ]
Cline, Gary W. [1 ]
Dufour, Sylvie [5 ]
Birkenfeld, Andreas L. [1 ]
Rothman, Douglas L. [3 ]
Carpenter, Thomas O. [4 ]
Insogna, Karl [1 ]
Petersen, Kitt Falk [1 ,6 ]
Bergwitz, Clemens [1 ]
Shulman, Gerald I. [1 ,2 ,5 ,6 ]
机构
[1] Yale Univ, Sch Med, Dept Internal Med, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Dept Cellular & Mol Physiol, New Haven, CT USA
[3] Yale Univ, Sch Med, Dept Radiol & Biomed Engn, New Haven, CT USA
[4] Yale Univ, Sch Med, Dept Pediat, New Haven, CT 06510 USA
[5] Yale Univ, Sch Med, Howard Hughes Med Inst, 300 Cedar St, New Haven, CT 06510 USA
[6] Univ Copenhagen, Novo Nordisk Fdn, Ctr Basic Metab Res, Copenhagen, Denmark
基金
美国国家卫生研究院; 奥地利科学基金会;
关键词
P-31]MRS; saturation transfer; inorganic phosphate; OXIDATIVE-PHOSPHORYLATION; INORGANIC-PHOSPHATE; SKELETAL-MUSCLE; IN-VIVO; MITOCHONDRIAL; HYPERCALCIURIA; MICE; DYSFUNCTION; MUTATIONS; WEAKNESS;
D O I
10.1096/fj.201600473R
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hypophosphatemia can lead to muscle weakness and respiratory and heart failure, but the mechanism is unknown. To address this question, we noninvasively assessed rates of muscle ATP synthesis in hypophosphatemic mice by using in vivo saturation transfer [P-31]-magnetic resonance spectroscopy. By using this approach, we found that basal and insulin-stimulated rates of muscle ATP synthetic flux (V-ATP) and plasma inorganic phosphate (P-i) were reduced by 50% in mice with diet-induced hypophosphatemia as well as in sodium-dependent P-i transporter solute carrier family 34, member 1 (NaPi2a)-knockout (NaPi2a(-/-)) mice compared with their wild-type littermate controls. Rates of V-ATP normalized in both hypophosphatemic groups after restoring plasma P-i concentrations. Furthermore, V-ATP was directly related to cellular and mitochondrial P-i uptake in L6 and RC13 rodent myocytes and isolated muscle mitochondria. Similar findings were observed in a patient with chronic hypophosphatemia as a result of a mutation in SLC34A3 who had a 50% reduction in both serum P-i content and muscle V-ATP. After oral P-i repletion and normalization of serum P-i levels, muscle V-ATP completely normalized in the patient. Taken together, these data support the hypothesis that decreased muscle ATP synthesis, in part, may be caused by low blood P-i concentrations, which may explain some aspects of muscle weakness observed in patients with hypophosphatemia.-Pesta, D. H., Tsirigotis, D. N., Befroy, D. E., Caballero, D., Jurczak, M. J., Rahimi, Y., Cline, G. W., Dufour, S., Birkenfeld, A. L., Rothman, D. L., Carpenter, T. O., Insogna, K., Petersen, K. F., Bergwitz, C., Shulman, G. I. Hypophosphatemia promotes lower rates of muscle ATP synthesis.
引用
收藏
页码:3378 / 3387
页数:10
相关论文
共 44 条
[1]   Hypophosphatemia: an evidence-based approach to its clinical consequences and management [J].
Amanzadeh, J ;
Reilly, RF .
NATURE CLINICAL PRACTICE NEPHROLOGY, 2006, 2 (03) :136-148
[2]   Muscle strength in type 2 diabetes [J].
Andersen, H ;
Nielsen, S ;
Mogensen, CE ;
Jakobsen, J .
DIABETES, 2004, 53 (06) :1543-1548
[3]   Muscle weakness - A progressive late complication in diabetic distal symmetric polyneuropathy [J].
Andreassen, CS ;
Jakobsen, J ;
Andersen, H .
DIABETES, 2006, 55 (03) :806-812
[4]   Modeling of oxygen transport and cellular energetics explains observations on in vivo cardiac energy metabolism [J].
Beard, Daniel A. .
PLOS COMPUTATIONAL BIOLOGY, 2006, 2 (09) :1093-1106
[5]   Targeted inactivation of Npt2 in mice leads to severe renal phosphate wasting, hypercalciuria, and skeletal abnormalities [J].
Beck, L ;
Karaplis, AC ;
Amizuka, N ;
Hewson, AS ;
Ozawa, H ;
Tenenhouse, HS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (09) :5372-5377
[6]   The Phosphate Transporter PiT1 (Slc20a1) Revealed As a New Essential Gene for Mouse Liver Development [J].
Beck, Laurent ;
Leroy, Christine ;
Beck-Cormier, Sarah ;
Forand, Anne ;
Salauen, Christine ;
Paris, Nadine ;
Bernier, Adeline ;
Urena-Torres, Pablo ;
Prie, Dominique ;
Ollero, Mario ;
Coulombel, Laure ;
Friedlander, Gerard .
PLOS ONE, 2010, 5 (02)
[7]   SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in maintaining phosphate homeostasis [J].
Bergwitz, C ;
Roslin, NM ;
Tieder, M ;
Loredo-Osti, JC ;
Bastepe, M ;
Abu-Zahra, H ;
Frappier, D ;
Burkett, K ;
Carpenter, O ;
Anderson, D ;
Garabédian, M ;
Sermet, I ;
Fujiwara, TM ;
Morgan, K ;
Tenenhouse, HS ;
Jüppner, H .
AMERICAN JOURNAL OF HUMAN GENETICS, 2006, 78 (02) :179-192
[8]   Phosphatonins and the regulation of phosphate homeostasis [J].
Berndt, Theresa ;
Kumar, Rajiv .
ANNUAL REVIEW OF PHYSIOLOGY, 2007, 69 :341-359
[9]   MRI detects early hindlimb muscle atrophy in Gly93Ala superoxide dismutase-1 (G93A SOD1) transgenic mice, an animal model of familial amyotrophic lateral sclerosis [J].
Brooks, KJ ;
Hill, MDW ;
Hockings, PD ;
Reid, DG .
NMR IN BIOMEDICINE, 2004, 17 (01) :28-32
[10]  
CAMP MA, 1990, MINER ELECTROL METAB, V16, P365