1 / 31

Before we begin…….

Before we begin……. Which of the B vitamins is the other name for Niacin? . B1 B3 B5 B7. Which of the B vitamins is the other name for Niacin? . B1 B3 B5 B7. Which amino acid can Niacin be synthesized from? . Proline Alanine Tryptophan Tyrosine.

ebony
Télécharger la présentation

Before we begin…….

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Before we begin…….

  2. Which of the B vitamins is the other name for Niacin? • B1 • B3 • B5 • B7

  3. Which of the B vitamins is the other name for Niacin? • B1 • B3 • B5 • B7

  4. Which amino acid can Niacin be synthesized from? • Proline • Alanine • Tryptophan • Tyrosine

  5. Which amino acid can Niacin be synthesized from? • Proline • Alanine • Tryptophan • Tyrosine

  6. Niacin deficiency can lead to: • Anemia • Seizures • Scurvy • Pellagra

  7. Niacin deficiency can lead to: • Anemia • Seizures • Scurvy • Pellagra

  8. Niacin Kirsten Boestfleisch, Lindsay Edmonds, Lena Husnay, Sarah Johnson

  9. Niacin • Vitamin B3 or nicotinic acid • Inositol hexaniacinate is also another form • Directly converted to nicotinamide • Niacin, nicotinic acid, and nicotinamide are cofactors for: • NAD+ • NADP+ *Both are involved in energy production • Water soluble (body does not store it) • Highest concentrations are found in the liver as NAD+ Niacin commons.wikimedia.org Nicotinamide

  10. Food Sources • Plant products • Wheat bran • Corn • Enriched breads and cereals • Legumes • Nuts • Meat products – NAD+ and NADP coenzymes • Released during cooking • Need fortification

  11. Why is Niacin Necessary? • Necessary for the metabolism of carbohydrates into glucose, which is used for energy • Helps the body use fat and protein • Boost immune system to fight disease • Healthy liver • Proper function of the nervous system • Improves circulation

  12. Synthesis from Tryptophan • Nicotinamide can be synthesized from tryptophan • Inefficient process: 1 mg of niacin needs 60 mg of tryptophan • Niacin deficiency oftentimes results when both niacin and tryptophan levels are insufficient

  13. Major Functions 1. Energy metabolism – NAD+ is reduced to NADH in several reactions: • Glycolytic reactions • Oxidative decarboxylation of pyruvate • Oxidation of acetate in the TCA cycle • Oxidation of alcohol • Beta oxidation of fatty acids • Many other cellular oxidation reactions Oxidation of NADH allows transfer of electrons in the electron transport chain to produce ATP.

  14. Major Functions Continued 2. NADP+ is reduced to NADPH • Pentose phosphate pathway • Malate-pyruvate shuttle (crosses mitochondrial membrane) NADPH becomes a reducing agent for many cellular macromolecules, manufacture of deoxyribonucleotides, cholesterol synthesis, and fatty acid production.

  15. Major Functions Continued 3. Poly(ADP-ribosyl)ation reactions • DNA metabolism and genomic stability 4. Mono(ADP-ribosyl)ation reactions • ADP-ribose attaches to amino acid side chains to make mono(ADP-ribose) • Aids cyclic ADP-ribose and NAADP formation • Allows control of intracellular calcium levels = cellular signaling

  16. Major Functions Continued *Cyclic ADP-ribose • Synthesis: ADP-ribose attaches to an internal ribose linkage • Important regulator of the CICR (calcium-induced calcium release) • Other regulators of calcium release: • Inositol-1,4,5-triphosphate (IP3) - a type of calcium channel • NAADP (a contaminate of NADP found to mobilize calcium)

  17. Major Functions continued 5. SIR2 (rats)/SIRT1 (humans) deacetylation reactions • Involved in genomic stability and expression particularly through: • Histones – involved in DNA transcription • Protein p53 – tumor suppressor A deficiency in niacin could result in a more active gene expression in DNA, making DNA more susceptible to structural damage.

  18. Specific Absorption • Some in stomach lining • Mostly in small intestine • At low concentrations: • Sodium-dependent facilitated diffusion • Carrier-mediated transport • Anion antiporters

  19. Transport Mechanism • Portal circulation • Facilitated diffusion into erythrocytes • Nicotinic acid or nicotinamide • Liver • Formation of NAD from tryptophan, nicotinamide, or nicotinic acid • Products for urinary excretion

  20. Mechanism of Action on Various Tissues

  21. 1 & 2: Niacin Action in the Adipose Tissue • Affects: adipocyte • Targets: HCAR2 receptor • Leads to: • Decreased lipolysis • Decreased VLDL and triglycerides

  22. 3 & 4: Niacin Action in the Artery • Affects: endothelium • Targets: • NAD+ phosphate • Lowers LDL oxidation – Decreases vascular inflammation • Redox sensitive genes • Lowers MCP-1 and VCAM-1 – Decreases vascular inflammation

  23. 5-7: Niacin Action in the Liver • Affects: hepatocyte • Targets: • Enzyme/receptor DGAT2 • Decreases triglyceride synthesis and Apo B secretion – Lowers VLDL and triglycerides, Apo B, and increases LDL particle size • Beta-chain ATP synthase • Lowers HDL catabolism – Increases lipoprotein A-1 and HDL2

  24. Toxicity • Short-term: • Vasodilation • Flushing • Burning in the face and hands • Nausea and vomiting *High dose is considered over 100mg per day • Long-term: • Hyperpigmentation • Abnormal glucose tolerance • Hyperuricemia • Peptic ulcers • Hepatomegaly • Jaundice

  25. Deficiency • Symptoms of mild deficiency: indigestion, fatigue, canker sores, vomiting, depression • Pellagra is associated with severe deficiency • Characterized by the four D’s: • Diarrhea • Dementia • Sun-sensitive dermatitis • Even death • Associated with AIDS, alcohol abuse, anorexia nervosa, cancer patients

  26. Pellagra Continued • “Casals Necklace” • Widespread in Europe in the 18th century • High incidence in SE states of the US During the early 20th century • associated with new imports of corn from Europe • Any guesses why? • Led to fortification of nicotinic acid and tryptophan in many foods www.odermatol.com

  27. Forms of Niacin as Supplements • Niacin used to treat: • Hartnup’s disease, poor glucose tolerance, IDDM, atherosclerosis, schizophrenia, hyperlipidemia, skin disorders • *Lipid soluble derivative of nicotinic acid for hyperlipidemia • Niacinamide used for: • Chemotherapy and also IDDM • Tablet or capsule • Regular or extended-released (fewer side effects but increased risk of liver damage) • *When supplementing with niacin, it is recommended that liver function tests be performed periodically

  28. Clinical Interactions • Antibiotics (tetracycline) • Aspirin • Anti-seizure medication • Anti-coagulants (blood thinners) • Blood pressure medications (Alpha-blockers) • Cholesterol-lowering medications • Statins • Diabetes medications • Isoniazid (INH) • Nicotine patches

  29. Take Away • Niacin supplies NAD+ to be reduced to NADH • Deficiencies lead to Pellagra • Niacin can improve cardiovascular health by increasing HDL and lowering LDL

  30. References • Brandt, Mark. “Vitamins and Coenzymes.” Chemistry and Biochemistry. Rose-Hulman Institute of Technology, n.d. Wed. 18 Nov. 2013. <http://www.rose-hulman.edu/~brandt/Chem330/Vitamin.pdf>. • “B-Vitamins and Folate.” Eat Right. Academy of Nutrition and Dietetics, n.d. Web. 17 Nov. 2013. <http://eatright.org/Public/content.aspx?id=6793>. • Creider JC, Hegele RA, Joy TR. Niacin: another look at an underutilized lipid-lowering medication. Nat Rev Endocrinol. 2012;8(9):517-28. • Kamanna VS, Kashyap ML. Mechanism of action of niacin. Am J Cardiol. 2008;101(8A):20B-26B. • Lavigne PM, Karas RH. The current state of niacin in cardiovascular disease prevention: a systematic review and meta-regression. J Am CollCardiol. 2013;61(4):440-6. • “New Lowdown on Cholesterol.” Havard Health Publications. Havard Medical School, n.d. Web. 18 Nov. 2013. <http://www.health.havard.edu/newsweek/New_lowdown_on_cholesterol.htm>. • “Niacin.” Medline Plus. National Institutes of Health, n.d. Web. 19 Nov. 2013. <http:/www.nlm.nih.gov/medlineplus/ency/article/002409.htm>. • “Niacin.” NMS Labs. Tox Wiki, n.d. Web. 20 Nov. 2013. <http://toxwiki.wikispaces.com/Niacin>. • Rhodes T, Norquist JM, Sisk CM, et al. The association of flushing bother, impact, treatment satisfaction and discontinuation of niacin therapy. Int J ClinPract. 2013;67(12):1238-46. • “Vitamin B3 (Niacin).” University of Maryland Medical Center. N.p., 20 June 2013. Web. 17 Nov. 2013. <http://umm.edu/health/medical/altmed/spplement/vitamin-b3--niacin>. • Zempleni J, Rucker RB, McCormick DB, Suttie JW. (2007) Handbook of Vitamins, pp. 1-570. CRC Press, Boca Raton FL.

More Related