Maternal Leucine-Rich Diet Minimises Muscle Mass Loss in Tumour-bearing Adult Rat Offspring by Improving the Balance of Muscle Protein Synthesis and Degradation
Cachexia syndrome can affect cancer patients and new prevention strategies are required. Maternal nutritional supplementation can modify metabolic programming in the offspring, which lasts until adulthood. This could be a good approach against diseases such as cancer. A 3% leucine-rich diet treatmen...
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Published in | Biomolecules (Basel, Switzerland) Vol. 9; no. 6; p. 229 |
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Language | English |
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Abstract | Cachexia syndrome can affect cancer patients and new prevention strategies are required. Maternal nutritional supplementation can modify metabolic programming in the offspring, which lasts until adulthood. This could be a good approach against diseases such as cancer. A 3% leucine-rich diet treatment improved muscle protein turnover by modifying the mTOR and proteolytic pathways, thus we analysed whether maternal supplementation could ameliorate muscle protein turnover in adult offspring tumour-bearing rats. Pregnant Wistar rats received a control diet or 3% leucine-rich diet during pregnancy/lactation, and their weaned male offspring received a control diet until adulthood when they were distributed into following groups (n = 7-8 per group): C, Control; W, tumour-bearing; L, without tumour with a maternal leucine-rich diet; and WL, tumour-bearing with a maternal leucine-rich diet. Protein synthesis and degradation were assessed in the gastrocnemius muscle, focusing on the mTOR pathway, which was extensively altered in W group. However, the WL adult offspring showed no decrease in muscle weight, higher food intake, ameliorated muscle turnover, activated mTOR and p70S6K, and maintained muscle cathepsin H and calpain activities. Maternal leucine nutritional supplementation could be a positive strategy to improve muscle protein balance in cancer cachexia-induced muscle damage in adult offspring rats. |
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AbstractList | Cachexia syndrome can affect cancer patients and new prevention strategies are required. Maternal nutritional supplementation can modify metabolic programming in the offspring, which lasts until adulthood. This could be a good approach against diseases such as cancer. A 3% leucine-rich diet treatment improved muscle protein turnover by modifying the mTOR and proteolytic pathways, thus we analysed whether maternal supplementation could ameliorate muscle protein turnover in adult offspring tumour-bearing rats. Pregnant Wistar rats received a control diet or 3% leucine-rich diet during pregnancy/lactation, and their weaned male offspring received a control diet until adulthood when they were distributed into following groups (n = 7−8 per group): C, Control; W, tumour-bearing; L, without tumour with a maternal leucine-rich diet; and WL, tumour-bearing with a maternal leucine-rich diet. Protein synthesis and degradation were assessed in the gastrocnemius muscle, focusing on the mTOR pathway, which was extensively altered in W group. However, the WL adult offspring showed no decrease in muscle weight, higher food intake, ameliorated muscle turnover, activated mTOR and p70S6K, and maintained muscle cathepsin H and calpain activities. Maternal leucine nutritional supplementation could be a positive strategy to improve muscle protein balance in cancer cachexia-induced muscle damage in adult offspring rats. Cachexia syndrome can affect cancer patients and new prevention strategies are required. Maternal nutritional supplementation can modify metabolic programming in the offspring, which lasts until adulthood. This could be a good approach against diseases such as cancer. A 3% leucine-rich diet treatment improved muscle protein turnover by modifying the mTOR and proteolytic pathways, thus we analysed whether maternal supplementation could ameliorate muscle protein turnover in adult offspring tumour-bearing rats. Pregnant Wistar rats received a control diet or 3% leucine-rich diet during pregnancy/lactation, and their weaned male offspring received a control diet until adulthood when they were distributed into following groups (n = 7–8 per group): C, Control; W, tumour-bearing; L, without tumour with a maternal leucine-rich diet; and WL, tumour-bearing with a maternal leucine-rich diet. Protein synthesis and degradation were assessed in the gastrocnemius muscle, focusing on the mTOR pathway, which was extensively altered in W group. However, the WL adult offspring showed no decrease in muscle weight, higher food intake, ameliorated muscle turnover, activated mTOR and p70S6K, and maintained muscle cathepsin H and calpain activities. Maternal leucine nutritional supplementation could be a positive strategy to improve muscle protein balance in cancer cachexia-induced muscle damage in adult offspring rats. |
Author | Gomes-Marcondes, Maria Cristina Cintra Oliveira, Sarah Christine Pereira de Miyaguti, Natália Angelo da Silva |
AuthorAffiliation | Laboratory of Nutrition and Cancer, Department of Structural and Functional Biology, Biology Institute, University of Campinas, UNICAMP, Rua Monteiro Lobato, 255, Campinas, São Paulo 13083862, Brazil; namiyaguti@gmail.com (N.A.d.S.M.); sarah.pe9@gmail.com (S.C.P.d.O.) |
AuthorAffiliation_xml | – name: Laboratory of Nutrition and Cancer, Department of Structural and Functional Biology, Biology Institute, University of Campinas, UNICAMP, Rua Monteiro Lobato, 255, Campinas, São Paulo 13083862, Brazil; namiyaguti@gmail.com (N.A.d.S.M.); sarah.pe9@gmail.com (S.C.P.d.O.) |
Author_xml | – sequence: 1 givenname: Natália Angelo da Silva orcidid: 0000-0003-4446-7924 surname: Miyaguti fullname: Miyaguti, Natália Angelo da Silva email: namiyaguti@gmail.com organization: Laboratory of Nutrition and Cancer, Department of Structural and Functional Biology, Biology Institute, University of Campinas, UNICAMP, Rua Monteiro Lobato, 255, Campinas, São Paulo 13083862, Brazil. namiyaguti@gmail.com – sequence: 2 givenname: Sarah Christine Pereira de surname: Oliveira fullname: Oliveira, Sarah Christine Pereira de email: sarah.pe9@gmail.com organization: Laboratory of Nutrition and Cancer, Department of Structural and Functional Biology, Biology Institute, University of Campinas, UNICAMP, Rua Monteiro Lobato, 255, Campinas, São Paulo 13083862, Brazil. sarah.pe9@gmail.com – sequence: 3 givenname: Maria Cristina Cintra orcidid: 0000-0002-1713-756X surname: Gomes-Marcondes fullname: Gomes-Marcondes, Maria Cristina Cintra email: cintgoma@unicamp.br organization: Laboratory of Nutrition and Cancer, Department of Structural and Functional Biology, Biology Institute, University of Campinas, UNICAMP, Rua Monteiro Lobato, 255, Campinas, São Paulo 13083862, Brazil. cintgoma@unicamp.br |
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Keywords | muscle protein turnover branched-chain amino acid maternal influence cancer cachexia |
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SubjectTerms | Animals Body Weight - drug effects branched-chain amino acid Cachexia - complications Cachexia - metabolism Cachexia - pathology cancer cachexia Diet Eating - drug effects Female Leucine - analysis Male maternal influence Mothers muscle protein turnover Muscle Proteins - biosynthesis Muscle Proteins - metabolism Muscle, Skeletal - drug effects Muscle, Skeletal - metabolism Muscle, Skeletal - pathology Muscles - drug effects Muscles - metabolism Muscles - pathology Neoplasms - complications Organ Size - drug effects Pregnancy Proteolysis - drug effects Rats Rats, Wistar |
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Title | Maternal Leucine-Rich Diet Minimises Muscle Mass Loss in Tumour-bearing Adult Rat Offspring by Improving the Balance of Muscle Protein Synthesis and Degradation |
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