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基于营养基因组学的精准抗肥胖治疗和预防假说:我们是否应该针对肌少症引起的大脑功能障碍?

Hypothesizing Nutrigenomic-Based Precision Anti-Obesity Treatment and Prophylaxis: Should We Be Targeting Sarcopenia Induced Brain Dysfunction?

机构信息

Center for Psychiatry, Medicine & Primary Care (Office of the Provost), Division of Addiction Research & Education, Western University Health Science, Pomona, CA 91766, USA.

Institute of Psychology, ELTE Eötvös Loránd University, Kazinczy u. 23-27, 1075 Budapest, Hungary.

出版信息

Int J Environ Res Public Health. 2021 Sep 16;18(18):9774. doi: 10.3390/ijerph18189774.

DOI:10.3390/ijerph18189774
PMID:34574696
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8470221/
Abstract

The United States Centers for Disease Control and Prevention (CDC) estimates a total obesity rate of 30% for 12 states and a 20% obesity rate nationwide. The obesity epidemic continues to increase in spite of preventative measures undertaken worldwide. Pharmacological treatments promise to reduce total fat mass. However, medications may have significant side effects and can be potentially fatal. : This brief review, based on a PUBMED search of the key terms "Obesity" and" Sarcopenia," will present evidence to corroborate the existence of Reward Deficiency Syndrome (RDS) in obesity and the involvement of catecholaminergic pathways in substance seeking behavior, particularly as it relates to carbohydrates cravings. The genetic basis and future genetic testing of children for risk of aberrant generalized craving behavior are considered a prevention method. Here we present evidence supporting the use of precursor amino acid therapy and modulation of enkephalinase, , and inhibition in key brain regions. Such treatments manifest in improved levels of dopamine/norepinephrine, GABA, serotonin, and enkephalins. We also present evidence substantiating insulin sensitivity enhancement via Chromium salts, which affect dopamine neuronal synthesis regulation. We believe our unique combination of natural ingredients will influence many pathways leading to the promotion of well-being and normal healthy metabolic functioning. Sarcopenia has been shown to reduce angiogenesis and possible cerebral blood flow. Exercise seems to provide a significant benefit to overcome this obesity-promoting loss of muscle density. Utilization of proposed nutrigenomic formulae based on coupling genetic obesity risk testing promotes generalized anti-craving of carbohydrates and can inhibit carbohydrate bingeing, inducing significant healthy fat loss and relapse prevention.

摘要

美国疾病控制与预防中心(CDC)估计,有 12 个州的总肥胖率为 30%,全国肥胖率为 20%。尽管全球都在采取预防措施,但肥胖症仍在持续增加。药物治疗有望减少总体脂肪量。然而,这些药物可能会产生严重的副作用,甚至可能是致命的。:本文基于对“肥胖症”和“肌肉减少症”这两个关键词在 PUBMED 上的搜索,简要回顾了现有文献,为肥胖症中存在奖励缺失综合征(RDS)以及儿茶酚胺能途径在物质寻求行为中的作用提供了证据,特别是与碳水化合物的渴望有关的物质寻求行为。考虑到异常广泛的渴望行为风险的儿童的遗传基础和未来的遗传检测可以作为一种预防方法。目前我们提供了证据支持使用前体氨基酸治疗和调节关键脑区的脑啡肽酶、和抑制,这种治疗方法表现为多巴胺/去甲肾上腺素、GABA、血清素和脑啡肽水平的提高。我们还提供了证据支持通过铬盐增强胰岛素敏感性,这会影响多巴胺神经元合成的调节。我们相信,我们独特的天然成分组合将影响许多途径,促进健康和正常的代谢功能。肌肉减少症已被证明会减少血管生成和可能的脑血流。运动似乎为克服肥胖症导致的肌肉密度下降提供了显著的益处。利用基于耦合遗传肥胖风险测试的拟议营养基因组配方可以促进对碳水化合物的普遍抗渴望,并可以抑制碳水化合物暴食,诱导显著的健康脂肪减少和预防复发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4589/8470221/e41287952c10/ijerph-18-09774-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4589/8470221/29e592e6fef4/ijerph-18-09774-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4589/8470221/d01f3e29e547/ijerph-18-09774-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4589/8470221/f55b82009de9/ijerph-18-09774-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4589/8470221/0215573430f7/ijerph-18-09774-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4589/8470221/05d646dbdf0e/ijerph-18-09774-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4589/8470221/e41287952c10/ijerph-18-09774-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4589/8470221/29e592e6fef4/ijerph-18-09774-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4589/8470221/d01f3e29e547/ijerph-18-09774-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4589/8470221/f55b82009de9/ijerph-18-09774-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4589/8470221/0215573430f7/ijerph-18-09774-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4589/8470221/05d646dbdf0e/ijerph-18-09774-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4589/8470221/e41287952c10/ijerph-18-09774-g006.jpg

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