User:Alexander Lee Schmidt/Sandbox 1
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== Function == | == Function == | ||
The mechanism for nitroglycerin breakdown is disputed, but it is know that nitroglycerin eventually breaks down into nitric oxide. In more recent years, nitroglycerin has been found to be broken down with the help of aldehyde dehydrogenase 2 found in the mitochondria. <ref>Mayer, B., and Beretta, M. (2008) The enigma of nitroglycerin bioactivation and nitrate tolerance. News, views, and troubles. Br. J. Pharmacol. 155, 170-184 </ref> | The mechanism for nitroglycerin breakdown is disputed, but it is know that nitroglycerin eventually breaks down into nitric oxide. In more recent years, nitroglycerin has been found to be broken down with the help of aldehyde dehydrogenase 2 found in the mitochondria. <ref>Mayer, B., and Beretta, M. (2008) The enigma of nitroglycerin bioactivation and nitrate tolerance. News, views, and troubles. Br. J. Pharmacol. 155, 170-184 </ref> | ||
- | There has been further proof showing that the breakdown of nitroglycerin permanently alters ALDH2 during | + | There has been further proof showing that the breakdown of nitroglycerin permanently alters ALDH2 during (<scene name='74/745476/Cys-302_of_aldh2_2/1'>Cys-302</scene>) attack <ref name="citation23"> Lang, Barbara S., Antonius Cf Gorren, Gustav Oberdorfer, M. Wenzl, Cristina M. Furdui, Leslie B. Poole, Bernd Mayer, and Karl Gruber. "Vascular Bioactivation of Nitroglycerin: Reaction Mechanism Revealed by Crystal Structure of Aldehyde Dehydrogenase-2." BMC Pharmacology and Toxicology BMC Pharmacol Toxicol 13.Suppl 1 (2012): n. pag. Web. 1 Nov. 2016.</ref>. |
The mechanism that is believed to happen takes nitroglycerin (GTN), bound to aldehyde dehydrogenase 2 (ALDH2) through hydrogen bonds and van der waal interactions of the terminal nitrates, then Cysteine-302 (in ALDH2) attacks GTN to form a thionitrate intermediate while also releasing 1,2-glyceryl dinitrate (1,2-GDN) and a small amount of nitric oxide (NO). The thionitrate is then attacked by the surrounding Cysteines (Cys-301 or Cys-303), which forms a disulfide bond and nitrite. The nitrite is then released and converted into NO. It has also been found that daidzin will inhibit GTN breakdown through competitive inhibition because the binding sites of daidzin and GTN overlap <ref name="citation23"> </ref>. Once NO is released it is believed to activate <scene name='74/745476/Guanylate_cyclase/1'>guanylate cyclase </scene>, resulting in an increase of guanosine 3'5' monophosphate (cyclic GMP) in smooth muscle and other tissues. These events lead to the dephosphorylation of myosin light chains, which regulate the contractile state in smooth muscle, and results in vasodilatation. <ref>"Nitrostat (Nitroglycerin) Drug Information: Clinical Pharmacology - Prescribing Information at RxList." RxList. N.p., n.d. Web. 30 Oct. 2016.</ref> | The mechanism that is believed to happen takes nitroglycerin (GTN), bound to aldehyde dehydrogenase 2 (ALDH2) through hydrogen bonds and van der waal interactions of the terminal nitrates, then Cysteine-302 (in ALDH2) attacks GTN to form a thionitrate intermediate while also releasing 1,2-glyceryl dinitrate (1,2-GDN) and a small amount of nitric oxide (NO). The thionitrate is then attacked by the surrounding Cysteines (Cys-301 or Cys-303), which forms a disulfide bond and nitrite. The nitrite is then released and converted into NO. It has also been found that daidzin will inhibit GTN breakdown through competitive inhibition because the binding sites of daidzin and GTN overlap <ref name="citation23"> </ref>. Once NO is released it is believed to activate <scene name='74/745476/Guanylate_cyclase/1'>guanylate cyclase </scene>, resulting in an increase of guanosine 3'5' monophosphate (cyclic GMP) in smooth muscle and other tissues. These events lead to the dephosphorylation of myosin light chains, which regulate the contractile state in smooth muscle, and results in vasodilatation. <ref>"Nitrostat (Nitroglycerin) Drug Information: Clinical Pharmacology - Prescribing Information at RxList." RxList. N.p., n.d. Web. 30 Oct. 2016.</ref> | ||
Revision as of 15:24, 1 December 2016
==NitroDur==
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delete these later
References
- ↑ 1.0 1.1 1.2 1.3 Tryzelaar, Dr. "Nitroglycerin (NTG)." Nitroglycerin (NTG). N.p., n.d. Web. 16 Oct. 2016”
- ↑ "NITRO-DUR® TRANSDERMAL DELIVERY SYSTEM." N.p., 3 Oct. 2014. Web. 16 Oct. 2016
- ↑ "Transderm Nitro (Nitroglycerin): Side Effects, Interactions, Warning, Dosage & Uses." RxList. N.p., 30 Mar. 2009. Web. 12 Nov. 2016.
- ↑ Mayer, B., and Beretta, M. (2008) The enigma of nitroglycerin bioactivation and nitrate tolerance. News, views, and troubles. Br. J. Pharmacol. 155, 170-184
- ↑ 5.0 5.1 Lang, Barbara S., Antonius Cf Gorren, Gustav Oberdorfer, M. Wenzl, Cristina M. Furdui, Leslie B. Poole, Bernd Mayer, and Karl Gruber. "Vascular Bioactivation of Nitroglycerin: Reaction Mechanism Revealed by Crystal Structure of Aldehyde Dehydrogenase-2." BMC Pharmacology and Toxicology BMC Pharmacol Toxicol 13.Suppl 1 (2012): n. pag. Web. 1 Nov. 2016.
- ↑ "Nitrostat (Nitroglycerin) Drug Information: Clinical Pharmacology - Prescribing Information at RxList." RxList. N.p., n.d. Web. 30 Oct. 2016.
- ↑ 7.0 7.1 Heer T, Reiter S, Trissler M, Hofling B, von Knobelsdorff-Brenkenhoff F, Pilz G. Effect of Nitroglycerin on the Performance of MR Coronary Angiography. J Magn Reson Imaging. 2016 Oct 12. doi: 10.1002/jmri.25483. PMID:27731913 doi:http://dx.doi.org/10.1002/jmri.25483
- ↑ Chronic Achilles Tendon Injury: An Overview." Hospital for Special Surgery. N.p., 1 June 2011. Web. 30 Oct. 2016
- ↑ Hunte G, Lloyd-Smith R. Topical glyceryl trinitrate for chronic Achilles tendinopathy. Clin J Sport Med. 2005 Mar;15(2):116-7. PMID:15782065
- ↑ Haythornthwaite, Jenifer, Dr., and Fredrick Wigley, Dr. "Raynaud's, Finger and Skin Care." Scleroderma Education Program Chapter 2 Raynaud’s, Finger and Skin Care (n.d.): n. pag. Web. 16 Oct. 2016