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      Diverging metabolic programmes and behaviours during states of starvation, protein malnutrition, and cachexia

      review-article
      , B.A. 1 , 2 , , M.D., Ph.D. 2 , 3 , , M.D., Ph.D. 3 , 4 , 5 ,
      Journal of Cachexia, Sarcopenia and Muscle
      John Wiley and Sons Inc.
      Starvation, Cachexia, Metabolism, Evolution, Protein malnutrition

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          Abstract

          Background

          Our evolutionary history is defined, in part, by our ability to survive times of nutrient scarcity. The outcomes of the metabolic and behavioural adaptations during starvation are highly efficient macronutrient allocation, minimization of energy expenditure, and maximized odds of finding food. However, in different contexts, caloric deprivation is met with vastly different physiologic and behavioural responses, which challenge the primacy of energy homeostasis.

          Methods

          We conducted a literature review of scientific studies in humans, laboratory animals, and non‐laboratory animals that evaluated the physiologic, metabolic, and behavioural responses to fasting, starvation, protein‐deficient or essential amino acid‐deficient diets, and cachexia. Studies that investigated the changes in ingestive behaviour, locomotor activity, resting metabolic rate, and tissue catabolism were selected as the focus of discussion.

          Results

          Whereas starvation responses prioritize energy balance, both protein malnutrition and cachexia present existential threats that induce unique adaptive programmes, which can exacerbate the caloric insufficiency of undernutrition. We compare and contrast the behavioural and metabolic responses and elucidate the mechanistic pathways that drive state‐dependent alterations in energy seeking and partitioning.

          Conclusions

          The evolution of energetically inefficient metabolic and behavioural responses to protein malnutrition and cachexia reveal a hierarchy of metabolic priorities governed by discrete regulatory networks.

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          Most cited references234

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          From inflammation to sickness and depression: when the immune system subjugates the brain.

          In response to a peripheral infection, innate immune cells produce pro-inflammatory cytokines that act on the brain to cause sickness behaviour. When activation of the peripheral immune system continues unabated, such as during systemic infections, cancer or autoimmune diseases, the ensuing immune signalling to the brain can lead to an exacerbation of sickness and the development of symptoms of depression in vulnerable individuals. These phenomena might account for the increased prevalence of clinical depression in physically ill people. Inflammation is therefore an important biological event that might increase the risk of major depressive episodes, much like the more traditional psychosocial factors.
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            Autophagy fights disease through cellular self-digestion.

            Autophagy, or cellular self-digestion, is a cellular pathway involved in protein and organelle degradation, with an astonishing number of connections to human disease and physiology. For example, autophagic dysfunction is associated with cancer, neurodegeneration, microbial infection and ageing. Paradoxically, although autophagy is primarily a protective process for the cell, it can also play a role in cell death. Understanding autophagy may ultimately allow scientists and clinicians to harness this process for the purpose of improving human health.
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              Identification and Importance of Brown Adipose Tissue in Adult Humans

              Obesity results from an imbalance between energy intake and expenditure. In rodents and newborn humans, brown adipose tissue helps regulate energy expenditure by thermogenesis mediated by the expression of uncoupling protein 1 (UCP1), but brown adipose tissue has been considered to have no physiologic relevance in adult humans. We analyzed 3640 consecutive (18)F-fluorodeoxyglucose ((18)F-FDG) positron-emission tomographic and computed tomographic (PET-CT) scans performed for various diagnostic reasons in 1972 patients for the presence of substantial depots of putative brown adipose tissue. Such depots were defined as collections of tissue that were more than 4 mm in diameter, had the density of adipose tissue according to CT, and had maximal standardized uptake values of (18)F-FDG of at least 2.0 g per milliliter, indicating high metabolic activity. Clinical indexes were recorded and compared with those of date-matched controls. Immunostaining for UCP1 was performed on biopsy specimens from the neck and supraclavicular regions in patients undergoing surgery. Substantial depots of brown adipose tissue were identified by PET-CT in a region extending from the anterior neck to the thorax. Tissue from this region had UCP1-immunopositive, multilocular adipocytes indicating brown adipose tissue. Positive scans were seen in 76 of 1013 women (7.5%) and 30 of 959 men (3.1%), corresponding to a female:male ratio greater than 2:1 (P<0.001). Women also had a greater mass of brown adipose tissue and higher (18)F-FDG uptake activity. The probability of the detection of brown adipose tissue was inversely correlated with years of age (P<0.001), outdoor temperature at the time of the scan (P=0.02), beta-blocker use (P<0.001), and among older patients, body-mass index (P=0.007). Defined regions of functionally active brown adipose tissue are present in adult humans, are more frequent in women than in men, and may be quantified noninvasively with the use of (18)F-FDG PET-CT. Most important, the amount of brown adipose tissue is inversely correlated with body-mass index, especially in older people, suggesting a potential role of brown adipose tissue in adult human metabolism. 2009 Massachusetts Medical Society
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                Author and article information

                Contributors
                grossber@ohsu.edu
                Journal
                J Cachexia Sarcopenia Muscle
                J Cachexia Sarcopenia Muscle
                10.1007/13539.2190-6009
                JCSM
                Journal of Cachexia, Sarcopenia and Muscle
                John Wiley and Sons Inc. (Hoboken )
                2190-5991
                2190-6009
                28 September 2020
                December 2020
                : 11
                : 6 ( doiID: 10.1002/jcsm.v11.6 )
                : 1429-1446
                Affiliations
                [ 1 ] Medical Scientist Training Program Oregon Health & Science University Portland OR USA
                [ 2 ] Papé Family Pediatric Research Institute Oregon Health & Science University Portland OR USA
                [ 3 ] Brenden‐Colson Center for Pancreatic Care Oregon Health & Science University Portland OR USA
                [ 4 ] Department of Radiation Medicine Oregon Health & Science University Portland OR USA
                [ 5 ] Cancer Early Detection Advanced Research Center Oregon Health & Science University Portland OR USA
                Author notes
                [*] [* ] Correspondence to: Aaron J. Grossberg, MD, PhD, Department of Radiation Medicine, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, L 481, Portland, OR 97239, USA. Email: grossber@ 123456ohsu.edu
                Author information
                https://orcid.org/0000-0003-2803-5363
                https://orcid.org/0000-0003-2675-7047
                https://orcid.org/0000-0003-4690-4948
                Article
                JCSM12630 JCSM-D-20-00095
                10.1002/jcsm.12630
                7749623
                32985801
                4b909e20-16c5-4f99-9c3b-61dad69388cf
                © 2020 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 26 February 2020
                : 04 September 2020
                : 07 September 2020
                Page count
                Figures: 4, Tables: 2, Pages: 18, Words: 7867
                Funding
                Funded by: Brenden‐Colson Center for Pancreatic Care
                Funded by: National Cancer Institute , open-funder-registry 10.13039/501100000095;
                Award ID: K08 CA245188
                Award ID: R01 CA234006
                Award ID: R01 CA217989
                Award ID: F30 CA254033
                Categories
                Review
                Reviews
                Custom metadata
                2.0
                December 2020
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.9.5 mode:remove_FC converted:19.12.2020

                Orthopedics
                starvation,cachexia,metabolism,evolution,protein malnutrition
                Orthopedics
                starvation, cachexia, metabolism, evolution, protein malnutrition

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