Non-classical role of vitamin D (Homo sapiens)
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Description
Vitamin D is known for its participation in various skeletal and non-skeletal muscle homeostasis. In addition to Calcium (Ca²⁺) and phosphorous (P) absorption, its association with CVD, hypertention, cancer, obesity, diabetes and immune system has been reported. It actively participates in the regulation of cardiovascular system through Renin Angiotensin Aldosterone System (RAAS). Renin is secreted by the kidney and it activates the formation of angiotensin II that leads to the decreased production of nitric oxide (NO) and increased endothelial vascular dysfunction (Pérez-Hernández et al., 2016). Vitamin D causes the insulin release, facilitates muscle contraction and glucose uptake by enhancing the activity of glucose transporter 4 (GLUT4) channels in the cells (Berridge, 2017) and reduces the aldosterone . From last few years vitamin D has gained special attention as immunomodulatory agent. The immunologic cells such as B cells, T cells, and antigen presenting cells express vitamin D receptors on their cells as well as are capable of synthesizing vitamin D metabolites especially calcitriol. The beneficial effects of vitamin D are linked with both innate and adaptive immune systems. During vitamin D deficiency an unwanted production of pro-inflammatory cytokines cause atherosclerotic lesions and atherogenesis. These conditions lead to increased vasoconstriction and decreased vasodilation, endothelial dysfunction, and alleviated nitric oxide formation. Furthermore, the expression of angiotensin-converting enzyme 2 (ACE2; responsible for the retrospective production of Ang1-7 form Ang II) is also reduced in vitamin D deficient subjects. Such individuals are more vulnerable to infectious diseases, especially, recent pandemic of COVID-19 (Malek Mahdavi, 2020).
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Ontology Terms
Bibliography
- Malek Mahdavi A; ''A brief review of interplay between vitamin D and angiotensin-converting enzyme 2: Implications for a potential treatment for COVID-19.''; Rev Med Virol, 2020 PubMed Europe PMC Scholia
- Berridge MJ; ''Vitamin D deficiency and diabetes.''; Biochem J, 2017 PubMed Europe PMC Scholia
- McLachlan CS; ''The angiotensin-converting enzyme 2 (ACE2) receptor in the prevention and treatment of COVID-19 are distinctly different paradigms.''; Clin Hypertens, 2020 PubMed Europe PMC Scholia
- Pérez-Hernández N, Aptilon-Duque G, Nostroza-Hernández MC, Vargas-Alarcón G, Rodríguez-Pérez JM, Blachman-Braun R; ''Vitamin D and its effects on cardiovascular diseases: a comprehensive review.''; Korean J Intern Med, 2016 PubMed Europe PMC Scholia
History
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External references
DataNodes
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Name | Type | Database reference | Comment |
---|---|---|---|
1,25-dihydroxycholecalciferol | Metabolite | CHEBI:17823 (ChEBI) | |
1-alpha- hydroxylase | Protein | V9GYP0 (Uniprot-TrEMBL) | |
25-hydroxycholecalciferol | Metabolite | CHEBI:17933 (ChEBI) | |
25-hydroxylase | Protein | E9PS56 (Uniprot-TrEMBL) | |
7-Dehydrocholesterol | Metabolite | CHEBI:17759 (ChEBI) | |
ACE2 | Protein | Q9BYF1 (Uniprot-TrEMBL) | |
ACE | Protein | A0A0A0MSN4 (Uniprot-TrEMBL) | |
Angiotensin II | Metabolite | HMDB01035 (HMDB) | |
Angiotensinogen | Protein | P01019 (Uniprot-TrEMBL) | |
Apoptosis | Pathway | WP254 (WikiPathways) | |
Cholecalciferol | Metabolite | CHEBI:28940 (ChEBI) | |
Fibrosis | Pathway | WP3624 (WikiPathways) | |
Inflammation | Pathway | WP4479 (WikiPathways) | |
ROS production | Pathway | WP4969 (WikiPathways) | |
Renal Type-1
angiotensin II receptor | Protein | P30556 (Uniprot-TrEMBL) | |
Renin | Protein | P00797 (Uniprot-TrEMBL) | |
Type-1
angiotensin II receptor | Protein | P30556 (Uniprot-TrEMBL) | |
Type-2
angiotensin II receptor | Protein | P50052 (Uniprot-TrEMBL) | |
Vasodilation | Pathway | WP4580 (WikiPathways) | |
aldosterone | Metabolite | Q184564 (Wikidata) | |
angiotensin I | Metabolite | CHEBI:2718 (ChEBI) | |
cytokines and inflammation | Pathway | WP530 (WikiPathways) | |
vitamin D receptor agonists | Metabolite | CHEBI:139503 (ChEBI) |
Annotated Interactions
No annotated interactions