Prazosin

Prazosin is an alpha-1 blocker medication primarily used to treat high blood pressure, symptoms of an enlarged prostate, and posttraumatic stress disorder (PTSD).[4] It is a less preferred treatment of high blood pressure.[4] Other uses may include heart failure and Raynaud syndrome.[5] It is taken by mouth.[4]

Prazosin
Clinical data
Trade namesMinipress, Vasoflex, Lentopres, others
AHFS/Drugs.comMonograph
MedlinePlusa682245
License data
Pregnancy
category
Addiction
liability		None
Routes of
administration		By mouth
ATC code
Legal status
Legal status
Pharmacokinetic data
Bioavailability~60%
Protein binding97%[2]
Onset of action30–90 minutes[3]
Elimination half-life2–3 hours[2]
Duration of action10–24 hours[2]
Identifiers
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.038.971
Chemical and physical data
FormulaC19H21N5O4
Molar mass383.408 g·mol−1
3D model (JSmol)
  (verify)

Common side effects include dizziness, sleepiness, nausea, and heart palpitations.[4] Serious side effects may include low blood pressure with standing and depression.[4][5] Prazosin is an α1-blocker.[4] It works to decrease blood pressure by dilating blood vessels and helps with an enlarged prostate by relaxing the outflow of the bladder.[4] How it works in PTSD is not entirely clear.[4]

Prazosin was patented in 1965 and came into medical use in 1974.[6] It is available as a generic medication.[4] In 2017, it was the 227th most commonly prescribed medication in the United States, with more than two million prescriptions.[7][8]

Medical use

Prazosin is active after oral administration and has a minimal effect on cardiac function due to its alpha-1 adrenergic receptor selectivity. When prazosin is started, however, heart rate and contractility can increase in order to maintain the pre-treatment blood pressures because the body has reached homeostasis at its abnormally high blood pressure. The blood pressure lowering effect becomes apparent when prazosin is taken for longer periods of time. The heart rate and contractility go back down over time and blood pressure decreases.

The antihypertensive characteristics of prazosin make it a second-line choice for the treatment of high blood pressure.[9]

Prazosin is also useful in treating urinary hesitancy associated with benign prostatic hyperplasia, blocking alpha-1 adrenergic receptors, which control constriction of both the prostate and urethra. Although not a first-line choice for either hypertension or benign prostatic hyperplasia, it is a choice for people who present with both problems concomitantly.[9]

There is some evidence that this medication is effective in treating nightmares, based on mixed results in randomized controlled trials. Prazosin was, however, shown to be more effective when treating nightmares related to PTSD.[10]

The drug is usually recommended for severe stings from the Indian red scorpion.[11][12][13]

Adverse effects

Common (4–10% frequency) side effects of prazosin include dizziness, headache, drowsiness, lack of energy, weakness, palpitations, and nausea.[14] Less frequent (1–4%) side effects include vomiting, diarrhea, constipation, edema, orthostatic hypotension, dyspnea, syncope, vertigo, depression, nervousness, and rash.[14] A very rare side effect of prazosin is priapism.[14][15] One phenomenon associated with prazosin is known as the "first dose response", in which the side effects of the drug – specifically orthostatic hypotension, dizziness, and drowsiness – are especially pronounced in the first dose.[14]

Orthostatic hypotension and syncope are associated with the body's poor ability to control blood pressure without active alpha-adrenergic receptors. People on prazosin should be told to rise to stand up slowly, since their poor baroreflex may cause them to faint if their blood pressure is not adequately maintained during standing. The nasal congestion is due to dilation of vessels in the nasal mucosa.

Mechanism of action

Prazosin is an α1-blocker that acts as an inverse agonist at alpha-1 adrenergic receptors, including α1A-, α1B-, and α1D-receptor subtypes.[16] These receptors are found on vascular smooth muscle, where they are responsible for the vasoconstrictive action of norepinephrine.[17] They are also found throughout the central nervous system.[18] Alpha-1 adrenergic receptors have been found on immune cells, where catecholamine binding can stimulate and enhance cytokine production.[19][20]

Research

Prazosin has been shown to prevent death in animal models of cytokine storm.[21] As a repurposed drug, prazosin is being investigated for the prevention of cytokine storm syndrome and complications of COVID-19 where it is thought to decrease cytokine dysregulation.[22][20][23]

References
  1. "Prazosin (Minipress) Use During Pregnancy". Drugs.com. 26 November 2019. Retrieved 30 January 2020.
  2. "Prazosin". drugs.com. Retrieved 15 March 2020.
  3. Packer M, Meller J, Gorlin R, Herman MV (March 1979). "Hemodynamic and clinical tachyphylaxis to prazosin-mediated afterload reduction in severe chronic congestive heart failure". Circulation. 59 (3): 531–9. doi:10.1161/01.cir.59.3.531. PMID 761333.
  4. "Prazosin Hydrochloride Monograph for Professionals". Drugs.com. American Society of Health-System Pharmacists. Retrieved 18 March 2019.
  5. British national formulary : BNF 76 (76 ed.). Pharmaceutical Press. 2018. p. 766. ISBN 9780857113382.
  6. Fischer, Jnos; Ganellin, C. Robin (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 455. ISBN 9783527607495.
  7. "The Top 300 of 2020". ClinCalc. Retrieved 11 April 2020.
  8. "Prazosin Hydrochloride - Drug Usage Statistics". ClinCalc. Retrieved 11 April 2020.
  9. Shen, Howard (2008). Illustrated Pharmacology Memory Cards: PharMnemonics. Minireview. p. 13. ISBN 978-1-59541-101-3.
  10. Kung S, Espinel Z, Lapid MI (September 2012). "Treatment of nightmares with prazosin: a systematic review". Mayo Clinic Proceedings. 87 (9): 890–900. doi:10.1016/j.mayocp.2012.05.015. PMC 3538493. PMID 22883741.
  11. Bawaskar HS, Bawaskar PH (2008). "Scorpion sting: A study of clinical manifestations and treatment regimes" (PDF). Current Science. 95 (9): 1337–1341. Retrieved 14 April 2010.
  12. Bawaskar HS, Bawaskar PH (January 2007). "Utility of scorpion antivenin vs prazosin in the management of severe Mesobuthus tamulus (Indian red scorpion) envenoming at rural setting" (PDF). The Journal of the Association of Physicians of India. 55: 14–21. PMID 17444339. Retrieved 14 April 2010.
  13. Pandi K, Krishnamurthy S, Srinivasaraghavan R, Mahadevan S (June 2014). "Efficacy of scorpion antivenom plus prazosin versus prazosin alone for Mesobuthus tamulus scorpion sting envenomation in children: a randomised controlled trial". Archives of Disease in Childhood. 99 (6): 575–80. doi:10.1136/archdischild-2013-305483. PMID 24550184. S2CID 37215729.
  14. "Minipress Prescribing Information" (PDF). United States Food and Drug Administration. Pfizer. February 2015. Retrieved 3 June 2016.
  15. Bhalla AK, Hoffbrand BI, Phatak PS, Reuben SR (October 1979). "Prazosin and priapism". British Medical Journal. 2 (6197): 1039. doi:10.1136/bmj.2.6197.1039. PMC 1596841. PMID 519276.
  16. "Prazosin: Biological activity". IUPHAR. International Union of Basic and Clinical Pharmacology. Retrieved 3 June 2016.
  17. "Prazosin: Clinical data". IUPHAR. International Union of Basic and Clinical Pharmacology. Retrieved 3 June 2016. This sympatholytic drug is used in the treatment of hypertension, anxiety and post-traumatic stress disorder. ... Antagonist of alpha-1 adrenoceptors on vascular smooth muscle, thereby inhibiting the vasoconstrictor effect of circulating and locally-released adrenaline and noradrenaline, resulting in peripheral vasodilation.
  18. Day HE, Campeau S, Watson SJ, Akil H (July 1997). "Distribution of alpha 1a-, alpha 1b- and alpha 1d-adrenergic receptor mRNA in the rat brain and spinal cord". Journal of Chemical Neuroanatomy. 13 (2): 115–39. doi:10.1016/S0891-0618(97)00042-2. PMID 9285356.
  19. Heijnen, Cobi J.; van der Voort, Charlotte Rouppe; Wulffraat, Nico; van der Net, Janjaap; Kuis, Wietse; Kavelaars, Annemieke (December 1996). "Functional α1-adrenergic receptors on leukocytes of patients with polyarticular juvenile rheumatoid arthritis". Journal of Neuroimmunology. 71 (1–2): 223–226. doi:10.1016/s0165-5728(96)00125-7. ISSN 0165-5728. PMID 8982123. S2CID 53151786.
  20. Konig, Maximilian F.; Powell, Michael A.; Staedtke, Verena; Bai, Ren-Yuan; Thomas, David L.; Fischer, Nicole M.; Huq, Sakibul; Khalafallah, Adham M.; Koenecke, Allison; Xiong, Ruoxuan; Mensh, Brett (30 April 2020). "Preventing cytokine storm syndrome in COVID-19 using α-1 adrenergic receptor antagonists". The Journal of Clinical Investigation. 130 (7): 3345–3347. doi:10.1172/JCI139642. ISSN 0021-9738. PMC 7324164. PMID 32352407.
  21. Staedtke, Verena; Bai, Ren-Yuan; Kim, Kibem; Darvas, Martin; Davila, Marco L.; Riggins, Gregory J.; Rothman, Paul B.; Papadopoulos, Nickolas; Kinzler, Kenneth W.; Vogelstein, Bert; Zhou, Shibin (December 2018). "Disruption of a self-amplifying catecholamine loop reduces cytokine release syndrome". Nature. 564 (7735): 273–277. doi:10.1038/s41586-018-0774-y. ISSN 1476-4687. PMC 6512810. PMID 30542164.
  22. "Preventing 'Cytokine Storm' May Ease Severe COVID-19 Symptoms". HHMI.org. Retrieved 24 May 2020.
  23. "Prazosin to Prevent COVID-19 (PREVENT-COVID Trial) - Full Text View - ClinicalTrials.gov". clinicaltrials.gov. Retrieved 24 May 2020.
  • "Prazosin". Drug Information Portal. U.S. National Library of Medicine.
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