Nitroglycerin (medication)

Common side effects include headache and low blood pressure.^[1] The low blood pressure can be severe.^[1] It is unclear if use in pregnancy is safe for the fetus.^[1] It should not be used together with medications within the PDE5 inhibitor family such as sildenafil due to the risk of low blood pressure.^[1] Nitroglycerin is in the nitrate family of medications.^[1] While it is not entirely clear how it works, it is believed to function by dilating blood vessels.^[1]

Nitroglycerin was written about as early as 1846^[5][6] and came into medical use in 1878.^[7][8][9] The drug nitroglycerin is a dilute form of the same chemical used as the explosive, nitroglycerin.^[9] Dilution makes it non-explosive.^[9] In 2021, it was the 174th most commonly prescribed medication in the United States, with more than 2 million prescriptions.^[10][11]

Nitroglycerin is used for the treatment of angina, acute myocardial infarction, severe hypertension, and acute coronary artery spasms.^[1][12] It may be administered intravenously, as a sublingual spray, or as a patch applied to the skin.

Glyceryl trinitrate is useful in decreasing angina attacks, perhaps more so than reversing angina once started, by supplementing blood concentrations of NO, also called endothelium-derived relaxing factor, before the structure of NO as the responsible agent was known. This led to the development of transdermal patches of glyceryl trinitrate, providing 24-hour release.^[13] However, the effectiveness of glyceryl trinitrate is limited by development of tolerance/tachyphylaxis within 2–3 weeks of sustained use. Continuous administration and absorption (such as provided by daily pills and especially skin patches) accelerate onset of tolerance and limit the usefulness of the agent. Thus, glyceryl trinitrate works best when used only in short-term, pulse dosing. Glyceryl trinitrate is useful for myocardial infarction (heart attack) and pulmonary edema, again working best if used quickly, within a few minutes of symptom onset, as a pulse dose. ^{[citation needed]}It may also be given as a sublingual or buccal dose in the form of a tablet placed under the tongue or a spray into the mouth for the treatment of an angina attack.^[14]

Tentative evidence indicates efficacy of glyceryl trinitrate in the treatment of various tendinopathies, both in pain management and acceleration of soft tissue repair.^{[15][16][17][18][19]}

Glyceryl trinitrate is also used in the treatment of anal fissures, though usually at a much lower concentration than that used for angina treatment.^[2]

Glyceryl trinitrate has been used to decrease pain associated with dysmenorrhea.^[3]

Glyceryl trinitrate was once researched for the prevention and treatment of osteoporosis; however, the researcher Sophie Jamal was found to have falsified the findings, sparking one of the largest scientific misconduct cases in Canada.^[20]

After long-term use for chronic conditions, nitrate tolerance—tolerance to agents such as glyceryl trinitrate— may develop in a patient, reducing its effectiveness. Tolerance is defined as the loss of symptomatic and hemodynamic effects of glyceryl trinitrate and/or the need for higher doses of the drug to achieve the same effects,^{[citation needed]} and was first described soon after the introduction of glyceryl trinitrate in cardiovascular therapy. Studies have shown^{[citation needed]} that nitrate tolerance is associated with vascular abnormalities which have the potential to worsen patients' prognosis.^{[21][full citation needed]} These include endothelial and autonomic dysfunction.^{[22][full citation needed]}

The mechanisms of nitrate tolerance have been investigated over the last 30 years, and several hypotheses to explain tolerance have been offered, including:

1. plasma volume expansion
2. impaired transformation of glyceryl trinitrate into NO or related species
3. counteraction of glyceryl trinitrate vasodilation by neurohormonal activation^[23]
4. oxidative stress^{[24][full citation needed]}

Glyceryl trinitrate can cause severe hypotension, reflex tachycardia, and severe headaches that necessitate analgesic intervention for pain relief, the painful nature of which can have a marked negative effect on patient compliance.

Glyceryl trinitrate also can cause severe hypotension, circulatory collapse, and death if used together with vasodilator drugs that are used for erectile dysfunction, such as sildenafil, tadalafil, and vardenafil.^[25]

Glyceryl trinitrate transdermal patches should be removed before defibrillation due to the risk of explosion and/or burns,^{[26][verification needed][better source needed]} but investigations have concluded that glyceryl trinitrate patch explosions during defibrillation were due to the breakdown voltage of the metal mesh in some patches.^{[27][non-primary source needed]}

Glyceryl trinitrate is a prodrug which must be denitrated, with the nitrite anion or a related species further reduced to produce the active metabolite nitric oxide (NO). Organic nitrates that undergo these two steps within the body are called nitrovasodilators, and the denitration and reduction occur via a variety of mechanisms. The mechanism by which such nitrates produce NO is widely disputed. Some believe^{[weasel words]} that organic nitrates produce NO by reacting with sulfhydryl groups, while others believe that enzymes such as glutathione S-transferases, cytochrome P450 (CYP), and xanthine oxidoreductase are the primary source of glyceryl trinitrate bioactivation. In recent years,^[when?] a great deal of evidence has been produced^{[citation needed]} that supports the conclusion that glyceryl trinitrate's clinically relevant denitration and reduction produce 1,2-glyceryl dinitrate (GDN) and NO, and that this reaction is catalysed by mitochondrial aldehyde dehydrogenase (ALDH2 or mtALDH).

The NO produced by this process is a potent activator of guanylyl cyclase (GC) by heme-dependent mechanisms; this activation results in formation of cyclic guanosine monophosphate (cGMP) from guanosine triphosphate (GTP). Among other roles, cGMP serves as a substrate for a cGMP-dependent protein kinase that activates myosin light chain phosphatase.^{[clarification needed]} Thus, production of NO from exogenous sources such as glyceryl trinitrate increases the level of cGMP within the cell, and stimulates dephosphorylation of myosin, which initiates relaxation of smooth muscle cells in blood vessels.

It was known almost from the time of the first synthesis of glyceryl trinitrate by Ascanio Sobrero in 1846 that handling and tasting of nitroglycerin could cause sudden intense headaches,^[5][6] which suggested a vasodilation effect (as suggested by Sobrero).^[28] Constantine Hering developed a form of nitroglycerin in 1847 and advocated for its dosing as a treatment of a number of diseases; however, its use as a specific treatment for blood pressure and chest pain was not among these. This is primarily due to his deep rooted focus in homeopathy.^[29][30]

Following Thomas Brunton's discovery that amyl nitrite could be used to treat chest pain, William Murrell experimented with the use of nitroglycerin to alleviate angina and reduce blood pressure, and showed that the accompanying headaches occurred as a result of overdose. Murrell began treating patients with small doses of glyceryl trinitrate in 1878, and the substance was widely adopted after he published his results in The Lancet in 1879.^[7]

The medical establishment used the name "glyceryl trinitrate" or "trinitrin" to avoid alarming patients, because of a general awareness that nitroglycerin was explosive.^{[31][verification needed]}

Overdoses may generate methemoglobinemia.^[32]

In the US, Nitrostat is marketed by Viatris after Upjohn was spun off from Pfizer.^[33][34][35]