Nicotinamide riboside supplementation confers marginal metabolic benefits in obese mice without remodeling the muscle acetyl-proteome.
Nicotinamide riboside supplementation confers marginal metabolic benefits in obese mice without remodeling the muscle acetyl-proteome.
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DOI:
10.1016/j.isci.2021.103635
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发表时间:
2022-01-21
期刊:
影响因子:
5.8
通讯作者:
Muoio DM
中科院分区:
文献类型:
--
作者:
Williams AS;Koves TR;Pettway YD;Draper JA;Slentz DH;Grimsrud PA;Ilkayeva OR;Muoio DM
Nicotinamide riboside supplements (NRS) have been touted as a nutraceutical that promotes cardiometabolic and musculoskeletal health by enhancing nicotinamide adenine dinucleotide (NAD+) biosynthesis, mitochondrial function, and/or the activities of NAD-dependent sirtuin deacetylase enzymes. This investigation examined the impact of NRS on whole body energy homeostasis, skeletal muscle mitochondrial function, and corresponding shifts in the acetyl-lysine proteome, in the context of diet-induced obesity using C57BL/6NJ mice. The study also included a genetically modified mouse model that imposes greater demand on sirtuin flux and associated NAD+ consumption, specifically within muscle tissues. In general, whole body glucose control was marginally improved by NRS when administered at the midpoint of a chronic high-fat diet, but not when given as a preventative therapy upon initiation of the diet. Contrary to anticipated outcomes, the study produced little evidence that NRS increases tissue NAD+ levels, augments mitochondrial function, and/or mitigates diet-induced hyperacetylation of the skeletal muscle proteome. Dietary NR supplementation (NRS) raises plasma and muscle NAM levels in obese mice NRS given post obesity slightly improved glucose control and mitochondrial function NRS did not oppose obesity-induced remodeling of the muscle acetyl-proteome NRS during weight gain did not protect glucose control and mitochondrial function Physiology; Proteomics; Nutrition
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影响因子:
16
作者:
Hirschey MD;Shimazu T;Jing E;Grueter CA;Collins AM;Aouizerat B;Stančáková A;Goetzman E;Lam MM;Schwer B;Stevens RD;Muehlbauer MJ;Kakar S;Bass NM;Kuusisto J;Laakso M;Alt FW;Newgard CB;Farese RV Jr;Kahn CR;Verdin E
通讯作者:
Verdin E
影响因子:
29
作者:
Frederick DW;Loro E;Liu L;Davila A Jr;Chellappa K;Silverman IM;Quinn WJ 3rd;Gosai SJ;Tichy ED;Davis JG;Mourkioti F;Gregory BD;Dellinger RW;Redpath P;Migaud ME;Nakamaru-Ogiso E;Rabinowitz JD;Khurana TS;Baur JA
通讯作者:
Baur JA
影响因子:
14.9
作者:
Deutsch EW;Csordas A;Sun Z;Jarnuczak A;Perez-Riverol Y;Ternent T;Campbell DS;Bernal-Llinares M;Okuda S;Kawano S;Moritz RL;Carver JJ;Wang M;Ishihama Y;Bandeira N;Hermjakob H;Vizcaíno JA
通讯作者:
Vizcaíno JA
影响因子:
2.9
作者:
Glancy, Brian;Willis, Wayne T.;Balaban, Robert S.
通讯作者:
Balaban, Robert S.
影响因子:
6.1
作者:
Crisol, Barbara M.;Veiga, Camilla B.;Ropelle, Eduardo R.
通讯作者:
Ropelle, Eduardo R.