Dietary choline intake: current state of knowledge across the life cycle

AM Wiedeman, SI Barr, TJ Green, Z Xu, SM Innis… - Nutrients, 2018 - mdpi.com
Choline, an essential dietary nutrient for humans, is required for the synthesis of the
neurotransmitter, acetylcholine, the methyl group donor, betaine, and phospholipids; and …

The controversial role of homocysteine in neurology: from labs to clinical practice

R Moretti, P Caruso - International journal of molecular sciences, 2019 - mdpi.com
Homocysteine (Hcy) is a sulfur-containing amino acid that is generated during methionine
metabolism. Physiologic Hcy levels are determined primarily by dietary intake and vitamin …

Homocysteine and hyperhomocysteinaemia

BL Zaric, M Obradovic, V Bajic… - Current medicinal …, 2019 - ingentaconnect.com
Homocysteine (Hcy) is a thiol group containing the amino acid, which naturally occurs in all
humans. Hcy is degraded in the body through two metabolic pathways, while a minor part is …

Sulfur amino acid metabolism: pathways for production and removal of homocysteine and cysteine

MH Stipanuk - Annu. Rev. Nutr., 2004 - annualreviews.org
▪ Abstract Tissue concentrations of both homocysteine (Hcy) and cysteine (Cys) are
maintained at low levels by regulated production and efficient removal of these thiols. The …

Folate and homocysteine metabolism in neural plasticity and neurodegenerative disorders

MP Mattson, TB Shea - Trends in neurosciences, 2003 - cell.com
Folate is a cofactor in one-carbon metabolism, during which it promotes the remethylation of
homocysteine–a cytotoxic sulfur-containing amino acid that can induce DNA strand …

The metabolism of homocysteine: pathways and regulation

JD Finkelstein - European journal of pediatrics, 1998 - Springer
Two pathways, the methionine cycle and transsulfuration, account for virtually all methionine
metabolism in mammals. Every tissue possesses the methionine cycle. Therefore, each can …

[HTML][HTML] Mechanisms of homocysteine neurotoxicity in neurodegenerative diseases with special reference to dementia

R Obeid, W Herrmann - FEBS letters, 2006 - Elsevier
Mild to moderate hyperhomocysteinemia is a risk factor for neurodegenerative diseases.
Human studies suggest that homocysteine (Hcy) plays a role in brain damage, cognitive and …

Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aortic lipid …

Z Chen, AC Karaplis, SL Ackerman… - Human molecular …, 2001 - academic.oup.com
Hyperhomocysteinemia, a risk factor for cardiovascular disease, is caused by nutritional
and/or genetic disruptions in homocysteine metabolism. The most common genetic cause of …

Hyperhomocysteinemia in end-stage renal disease: prevalence, etiology, and potential relationship to arteriosclerotic outcomes

AG Bostom, L Lathrop - Kidney international, 1997 - Elsevier
This review will first place hyperhomocysteinemia in the context of the other established
amino acid abnormalities characteristic of ESRD. What is known from studies of general and …

Pathways and regulation of homocysteine metabolism in mammals

J Finkelstein - Seminars in thrombosis and hemostasis, 2000 - thieme-connect.com
Two intersecting pathways, the methionine cycle and the transsulfuration sequence,
compose the mechanisms for homocysteine metabolism in mammals. The methionine cycle …