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protein

22 studies
A randomized 3-way crossover study indicates that high-protein feeding induces de novo lipogenesis in healthy humans
by Evelina Charidemou, Tom Ashmore, Xuefei Li, Ben D. McNally, James A. West, Sonia Liggi, Matthew Harvey, Elise Orford, Julian L. Griffin
Resistance exercise protects mice from protein-induced fat accretion
by Michaela E Trautman, Leah N Braucher, Christian Elliehausen, Wenyuan G Zhu, Esther Zelenovskiy, Madelyn Green, Michelle M Sonsalla, Chung-Yang Yeh, Troy A Hornberger, Adam R Konopka, Dudley W Lamming
Dietary restriction of isoleucine increases healthspan and lifespan of genetically heterogeneous mice
by Cara L.Green, Michaela E.Trautman, KrittisakChaiyakul, RaghavJain, Yasmine H.Alam, RejiBabygirija, Heidi H.Pak, Michelle M.Sonsalla, Mariah F.Calubag, Chung-YangYeh, AnnelieseBleicher, GraceNovak, Teresa T.Liu, SarahNewman, Will A.Ricke, Kristina A.Matkowskyj, Irene M.Ong, CholsoonJang, JudithSimcox, Dudley W.Lamming
Dietary isoleucine content defines the metabolic and molecular response to a Western diet
by Michaela E.Trautman, Cara L.Green, Michael R.MacArthur, KrittisakChaiyakul, Yasmine H.Alam, Chung-YangYeh, RejiBabygirija, IsabellaJames, MichaelGilpin, EstherZelenovskiy, MadelynGreen, Ryan N.Marshall, Michelle M.Sonsalla, VictoriaFlores, View ORCID ProfileJudith A.Simcox, Irene M.Ong, Kristen C.Malecki, CholsoonJang, View ORCID ProfileDudley W.Lamming
A 3-Week Tryptophan-Deficient Diet Resulted in Decreased Body Weight and Increased Trabecular Bone Mass in Mice
by Carlos Isales, Kehong Ding, Meghan McGee-Lawrence, Wendy Bollag, William Hill, Sadanand Fulzele, Mohamed Awad, Mark Hamrick
A Branched-Chain Amino Acid-Related Metabolic Signature that Differentiates Obese and Lean Humans and Contributes to Insulin Resistance
by Christopher B Newgard, Jie An, James R Bain, Michael J Muehlbauer, Robert D Stevens, Lillian F Lien, Andrea M Haqq, Svati H. Shah, Michelle Arlotto, Cris A Slentz, James Rochon, Dianne Gallup, Olga Ilkayeva, Brett R Wenner, William E Yancy, Howard Eisenson, Gerald Musante, Richard Surwit, David S Millington, Mark D Butler, Laura P Svetkey
A Novel Dietary Intervention Reduces Circulatory Branched-Chain Amino Acids by 50%: A Pilot Study of Relevance for Obesity and Diabetes
by Imran Ramzan, Moira Taylor, Beth Phillips, Daniel Wilkinson, Kenneth Smith, Kate Hession, Iskandar Idris, Philip Atherton
Restricting Branched-Chain Amino Acids within a High-Fat Diet Prevents Obesity
by Ming Liu, Yiheng Huang, Hongwei Zhang, Dawn Aitken, Michael C. Nevitt, Jason S. Rockel, Jean-Pierre Pelletier, Cora E. Lewis, James Torner, Yoga Raja Rampersaud, Anthony V. Perruccio, Nizar N. Mahomed, Andrew Furey, Edward W. Randell, Proton Rahman, Guang Sun, Johanne Martel-Pelletier, Mohit Kapoor, Graeme Jones, David Felson, Dake Qi, Guangju Zhai
Restoration of metabolic health by decreased consumption of branched‐chain amino acids
by Nicole E. Cummings, Elizabeth M. Williams, Ildiko Kasza, Elizabeth N. Konon, Michael D. Schaid, Brian A. Schmidt, Chetan Poudel, Dawn S. Sherman, Deyang Yu, Sebastian I. Arriola Apelo, Sara E. Cottrell, Gabriella Geiger, Macy E. Barnes, Jaclyn A. Wisinski, Rachel J. Fenske, Kristina A. Matkowskyj, Michelle E. Kimple, Caroline M. Alexander, Matthew J. Merrins, Dudley W. Lamming
Meta-analysis about the amounts & role of protein required to sustain lean body mass. "∼32–46 g of high-quality dietary protein/day is reported to be required to maintain protein balance (2). This is considerably less than amounts of protein reportedly consumed by American adults (∼65–100+ g/day)" The remaining protein is deaminated, turned into glucose, and oxidized as fuel. Many studies report that, despite this, feeding protein does not seem to increase blood glucose. This study fed doubly-labeled protein from whole eggs and traced how much of the glucose entering the bloodstream during the following 8h came from this protein. It ended up being only around 4%. It therefore seems that the process of gluconeogenesis is highly regulated, it's not that "excess protein automatically gets turned into glucose and dumped in the bloodstream."
Dietary Protein Restriction Improves Metabolic Dysfunction in Patients with Metabolic Syndrome in a Randomized, Controlled Trial
by Rafael Ferraz-Bannitz, Rebeca A. Beraldo, A. Augusto Peluso, Morten Dall, Parizad Babaei, Rayana Cardoso Foglietti, Larissa Marfori Martins, Patricia Moreira Gomes, Julio Sergio Marchini, Vivian Marques Miguel Suen, Luiz C. Conti de Freitas, Luiz Carlos Navegantes, Marco Antônio M. Pretti, Mariana Boroni, Jonas T. Treebak, Marcelo A. Mori, Milton Cesar Foss, Maria Cristina Foss-Freitas
In this Brazilian 27-day RCT, protein restriction had nearly the same effect on weight loss & glucose control as caloric restriction.
The adverse metabolic effects of branched-chain amino acids are mediated by isoleucine and valine
by DeyangYu12312, Nicole E.Richardson12412, Cara L.Green12, Alexandra B.Spicer5, Michaela E.Murphy126, VictoriaFlores126, CholsoonJang78, IldikoKasza9, MariaNikodemova5, Matthew H.Wakai12, Jay L.Tomasiewicz1, Shany E.Yang12, Blake R.Miller12, Heidi H.Pak12, Jacqueline A.Brinkman12, Jennifer M.Rojas10, William J.QuinnIII10, Eunhae P.Cheng12, Elizabeth N.Konon12, Lexington R.Haider12, Dudley W.Lamming123461113
Having previously established the positive effects of protein restriction, and having narrowed it down to BCAA restriction, this experiment sought to test which of the 3 BCAAs is mediating the effect. It turned out to be mostly isoleucine, with valine playing a smaller role. FGF21 was shown to be part of what mediated the effects of isoleucine restriction.
The article reviews the literature about the Randle cycle and mitochondrial inertia, and develops a model to explain how lipids and BCAAs play together to promote insulin resistance. A literature review shows that BCAAs are associated with insulin resistance and diabetes more than any other metabolite studied. Yet the negative effects of BCAAs only seem to show up in "high-fat" diets. The authors therefore believe that BCAAs can "clog up" the TCA cycle similarly to lipids, possibly competing for similar pathways. This can then lead to glucose intolerance.