Insulin resistance and glycine metabolism in humans
Plasma glycine level is low in patients with obesity or diabetes and the improvement of insulin resistance increases plasma glycine concentration. In prospective studies, hypoglycinemia at baseline predicts the risk of developing type 2 diabetes and higher serum glycine level is associated with decr...
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Published in | Amino acids Vol. 50; no. 1; pp. 11 - 27 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Vienna
Springer Vienna
01.01.2018
Springer Nature B.V |
Subjects | |
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Abstract | Plasma glycine level is low in patients with obesity or diabetes and the improvement of insulin resistance increases plasma glycine concentration. In prospective studies, hypoglycinemia at baseline predicts the risk of developing type 2 diabetes and higher serum glycine level is associated with decreased risk of incident type 2 diabetes. Consistently, plasma glycine concentration is lower in the lean offspring of parents with type 2 diabetes compared to healthy subjects. Among patients with type 2 diabetes, hypoglycinemia occurs before clinical manifestations of the disease, but the pathophysiological mechanisms underlying glycine deficit and its potential clinical repercussions are unclear. Glycine participates in several metabolic pathways, being required for relevant human physiological processes. Humans synthesize glycine from glyoxylate, glucose (via serine), betaine and likely from threonine and during the endogenous synthesis of L-carnitine. Glycine conjugates bile acids and other acyl moieties producing acyl-glycine derivatives. The glycine cleavage system catalyzes glycine degradation to carbon dioxide and ammonium while tetrahydrofolate is converted into 5,10-methylene-tetrahydrofolate. Glycine is utilized to synthesize serine, sarcosine, purines, creatine, heme group, glutathione, and collagen. Glycine is a major quantitative component of collagen. In addition, the role of glycine maintaining collagen structure is critical, as glycine residues are required to stabilize the triple helix of the collagen molecule. This quality of glycine likely contributes to explain the occurrence of medial arterial calcification and the elevated cardiovascular risk associated with diabetes and chronic kidney disease, as emerging evidence links normal collagen content with the initiation and progression of vascular calcification in humans. |
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AbstractList | Plasma glycine level is low in patients with obesity or diabetes and the improvement of insulin resistance increases plasma glycine concentration. In prospective studies, hypoglycinemia at baseline predicts the risk of developing type 2 diabetes and higher serum glycine level is associated with decreased risk of incident type 2 diabetes. Consistently, plasma glycine concentration is lower in the lean offspring of parents with type 2 diabetes compared to healthy subjects. Among patients with type 2 diabetes, hypoglycinemia occurs before clinical manifestations of the disease, but the pathophysiological mechanisms underlying glycine deficit and its potential clinical repercussions are unclear. Glycine participates in several metabolic pathways, being required for relevant human physiological processes. Humans synthesize glycine from glyoxylate, glucose (via serine), betaine and likely from threonine and during the endogenous synthesis of L-carnitine. Glycine conjugates bile acids and other acyl moieties producing acyl-glycine derivatives. The glycine cleavage system catalyzes glycine degradation to carbon dioxide and ammonium while tetrahydrofolate is converted into 5,10-methylene-tetrahydrofolate. Glycine is utilized to synthesize serine, sarcosine, purines, creatine, heme group, glutathione, and collagen. Glycine is a major quantitative component of collagen. In addition, the role of glycine maintaining collagen structure is critical, as glycine residues are required to stabilize the triple helix of the collagen molecule. This quality of glycine likely contributes to explain the occurrence of medial arterial calcification and the elevated cardiovascular risk associated with diabetes and chronic kidney disease, as emerging evidence links normal collagen content with the initiation and progression of vascular calcification in humans. Plasma glycine level is low in patients with obesity or diabetes and the improvement of insulin resistance increases plasma glycine concentration. In prospective studies, hypoglycinemia at baseline predicts the risk of developing type 2 diabetes and higher serum glycine level is associated with decreased risk of incident type 2 diabetes. Consistently, plasma glycine concentration is lower in the lean offspring of parents with type 2 diabetes compared to healthy subjects. Among patients with type 2 diabetes, hypoglycinemia occurs before clinical manifestations of the disease, but the pathophysiological mechanisms underlying glycine deficit and its potential clinical repercussions are unclear. Glycine participates in several metabolic pathways, being required for relevant human physiological processes. Humans synthesize glycine from glyoxylate, glucose (via serine), betaine and likely from threonine and during the endogenous synthesis of L-carnitine. Glycine conjugates bile acids and other acyl moieties producing acyl-glycine derivatives. The glycine cleavage system catalyzes glycine degradation to carbon dioxide and ammonium while tetrahydrofolate is converted into 5,10-methylene-tetrahydrofolate. Glycine is utilized to synthesize serine, sarcosine, purines, creatine, heme group, glutathione, and collagen. Glycine is a major quantitative component of collagen. In addition, the role of glycine maintaining collagen structure is critical, as glycine residues are required to stabilize the triple helix of the collagen molecule. This quality of glycine likely contributes to explain the occurrence of medial arterial calcification and the elevated cardiovascular risk associated with diabetes and chronic kidney disease, as emerging evidence links normal collagen content with the initiation and progression of vascular calcification in humans.Plasma glycine level is low in patients with obesity or diabetes and the improvement of insulin resistance increases plasma glycine concentration. In prospective studies, hypoglycinemia at baseline predicts the risk of developing type 2 diabetes and higher serum glycine level is associated with decreased risk of incident type 2 diabetes. Consistently, plasma glycine concentration is lower in the lean offspring of parents with type 2 diabetes compared to healthy subjects. Among patients with type 2 diabetes, hypoglycinemia occurs before clinical manifestations of the disease, but the pathophysiological mechanisms underlying glycine deficit and its potential clinical repercussions are unclear. Glycine participates in several metabolic pathways, being required for relevant human physiological processes. Humans synthesize glycine from glyoxylate, glucose (via serine), betaine and likely from threonine and during the endogenous synthesis of L-carnitine. Glycine conjugates bile acids and other acyl moieties producing acyl-glycine derivatives. The glycine cleavage system catalyzes glycine degradation to carbon dioxide and ammonium while tetrahydrofolate is converted into 5,10-methylene-tetrahydrofolate. Glycine is utilized to synthesize serine, sarcosine, purines, creatine, heme group, glutathione, and collagen. Glycine is a major quantitative component of collagen. In addition, the role of glycine maintaining collagen structure is critical, as glycine residues are required to stabilize the triple helix of the collagen molecule. This quality of glycine likely contributes to explain the occurrence of medial arterial calcification and the elevated cardiovascular risk associated with diabetes and chronic kidney disease, as emerging evidence links normal collagen content with the initiation and progression of vascular calcification in humans. |
Author | Donapetry-García, C. Adeva-Andany, M. Souto-Adeva, G. Fernández-Fernández, C. Domínguez-Montero, A. Ameneiros-Rodríguez, E. |
Author_xml | – sequence: 1 givenname: M. surname: Adeva-Andany fullname: Adeva-Andany, M. email: madevaa@yahoo.com organization: Internal Medicine Department, Hospital General Juan Cardona – sequence: 2 givenname: G. surname: Souto-Adeva fullname: Souto-Adeva, G. organization: National Institutes of Health, National Institute of Arthritis and Metabolic Diseases – sequence: 3 givenname: E. surname: Ameneiros-Rodríguez fullname: Ameneiros-Rodríguez, E. organization: Internal Medicine Department, Hospital General Juan Cardona – sequence: 4 givenname: C. surname: Fernández-Fernández fullname: Fernández-Fernández, C. organization: Internal Medicine Department, Hospital General Juan Cardona – sequence: 5 givenname: C. surname: Donapetry-García fullname: Donapetry-García, C. organization: Internal Medicine Department, Hospital General Juan Cardona – sequence: 6 givenname: A. surname: Domínguez-Montero fullname: Domínguez-Montero, A. organization: Internal Medicine Department, Hospital General Juan Cardona |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29094215$$D View this record in MEDLINE/PubMed |
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Keywords | Obesity Insulin resistance One-carbon metabolism Diabetes Glycine Serine hydroxymethyl transferase |
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PublicationDate | 2018-01-01 |
PublicationDateYYYYMMDD | 2018-01-01 |
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PublicationSubtitle | The Forum for Amino Acid, Peptide and Protein Research |
PublicationTitle | Amino acids |
PublicationTitleAbbrev | Amino Acids |
PublicationTitleAlternate | Amino Acids |
PublicationYear | 2018 |
Publisher | Springer Vienna Springer Nature B.V |
Publisher_xml | – name: Springer Vienna – name: Springer Nature B.V |
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SubjectTerms | Ammonium Analytical Chemistry Arteriosclerosis Betaine Bile acids Biochemical Engineering biochemical pathways Biochemistry Biomedical and Life Sciences blood serum Calcification Calcification (ectopic) Carbon dioxide Cardiovascular diseases Carnitine Collagen Creatine Diabetes Diabetes mellitus Diabetes mellitus (non-insulin dependent) Diabetes Mellitus, Type 2 - blood Diabetes Mellitus, Type 2 - metabolism Diabetes Mellitus, Type 2 - physiopathology glucose Glutathione Glycine Glycine - biosynthesis Glycine - blood Glycine - deficiency Glycine - metabolism Heme Humans Insulin Insulin resistance Insulin Resistance - physiology kidney diseases Kidney transplantation L-Carnitine Life Sciences Metabolic pathways Metabolism Models, Biological moieties Neurobiology noninsulin-dependent diabetes mellitus obesity Parents Patients progeny prospective studies Proteomics Purines Review Article Risk risk reduction Sarcosine Serine Synthesis Tetrahydrofolic acid Threonine |
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Title | Insulin resistance and glycine metabolism in humans |
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