Amrinone

Amrinone, also known as inamrinone, and sold as Inocor, is a pyridine phosphodiesterase 3 inhibitor.[1] It is a drug that may improve the prognosis in patients with congestive heart failure.[2] Amrinone has been shown to increase the contractions initiated in the heart by high-gain calcium induced calcium release (CICR).[3] The positive inotropic effect of amrinone is mediated by the selective enhancement of high-gain CICR, which contributes to the contraction of myocytes by phosphorylation through cAMP dependent protein kinase A (PKA) and Ca2+ calmodulin kinase pathways.[3]

Amrinone
Clinical data
Trade namesInocor
Other namesinamrinone (USAN US)
AHFS/Drugs.comInternational Drug Names
Routes of
administration		Intravenous
ATC code
Legal status
Legal status
  • In general: ℞ (Prescription only)
Pharmacokinetic data
Bioavailabilityn/a
Protein binding10 to 49%
MetabolismHepatic
Elimination half-life5 to 8 hours
ExcretionRenal (63%) and fecal (18%)
Identifiers
  • 5-amino-3,4'-bipyridin-6(1H)-one
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.056.700
Chemical and physical data
FormulaC10H9N3O
Molar mass187.202 g·mol−1
3D model (JSmol)
  • O=C2C(/N)=C\C(\c1ccncc1)=C/N2
  • InChI=1S/C10H9N3O/c11-9-5-8(6-13-10(9)14)7-1-3-12-4-2-7/h1-6H,11H2,(H,13,14) checkY
  • Key:RNLQIBCLLYYYFJ-UHFFFAOYSA-N checkY
  (verify)

Actions

Increases cardiac contractility, vasodilator. Acts by inhibiting the breakdown of both cAMP and cGMP by the phosphodiesterase (PDE3) enzyme. There is a long-standing controversy regarding whether the drug actually increases cardiac contractility in diseased myocardium (and therefore whether it is of any clinical use). The issue has been reviewed extensively by Dr Peter Wilmshurst, one of the first cardiologists and researchers to question the drug's efficacy.[4]

PDE-III inhibition and cardiac function

PDE III is present in cardiac muscle, vascular smooth muscle and platelets. PDE III degrades the phosphodiester bond in cAMP to break it down.[5][6] When PDE III is inhibited, cAMP cannot be inactivated. An increase in cAMP with the administration of amrinone in vascular smooth muscle produces vasodilation by facilitating calcium uptake by the sarcoplasmic reticulum (a special type of smooth ER) and decreasing the calcium available for contraction.[5][7] In myocytes, the increase of cAMP concentration increases in turn the activity of PKA; this kinase improves the Ca2+ inward current through the L-type Ca2+ channels, which leads to calcium-induced calcium release from the sarcoplasmic reticulum, giving rise to a calcium spark that triggers the contraction; this results in an inotropic effect. Furthermore, PKA phosphorylates and deactivates the phospholambans that inhibit SERCA, which is an enzymatic pump that, to terminate the contraction, removes the Ca2+ from the cytoplasm, stores it back in the sarcoplasmic reticulum and promotes the subsequent arterial relaxation as well, producing a lusitropic effect. Both inotropic and lusitropic effects justify the use of amrinone to treat heart failure. Amrinone decreases the pulmonary capillary wedge pressure while increasing cardiac output, as it functions as an arterial vasodilator and increases venous capacitance while decreasing venous return.[5] There is a net decrease in myocardial wall tension, and O2 consumption when using amrinone. Amrinone also has beneficial effects during diastole in the left ventricle, including relaxation, compliance and filling in patients with congestive heart failure.[5]

Indications

Short-term management of severe CHF (not used long term because of increased mortality, probably due to heart failure).

Effects in congestive heart failure

Congestive heart failure (CHF) is characterized by a reduction in ventricular performance and abnormalities in peripheral circulation and organs.[6] A reduced release of endothelium derived relaxing factor (EDRF) causes a decrease in the stimulation of guanylate cyclase, and cyclic GMP (cGMP) levels fall in vascular smooth muscle. This impairs relaxation in the vasculature and is a part of the vicious cycle of CHF.[6] Patients with CHF have a down-regulation of their β-1 adrenergic receptors which alters their ability to activate intracellular adenylate cyclase, which catalyzes cAMP formation.[5] cAMP is the second messenger that controls the level of calcium available to allow the heart to contract. An IV administration of amrinone has been shown to increase cardiac output (CO) and stroke volume (SV), while concurrently reducing the filling pressure of the left ventricle and decreasing the resistance in the peripheral vasculature.[2][8][9] This does not lead to an increase in heart rate or blood pressure.[2][8][9] The improvement in performance of the ventricles is likely to result from a direct stimulation of the depressed myocardium as well as a decrease in peripheral vascular resistance.[10]

Contraindications

Patients with aortic stenosis, hypertrophic cardiomyopathy, or history of hypersensitivity to the drug.

Precautions

May increase myocardial ischemia. Blood pressure, pulse, and ECG should be constantly monitored. Amrinone should only be diluted with normal saline or 1/2 normal saline; no dextrose solutions should be used. Furosemide, a loop diuretic, should not be administered into an IV line delivering amrinone.

Side effects

Thrombocytopenia is the most prominent and dose-related side effect, but it is transient and asymptomatic. Nausea, diarrhea, hepatotoxicity, arrhythmias and fever are other adverse effects.

Amrinone discovery and progression

Early studies in patients with heart failure showed that amrinone produced short-term hemodynamic improvement, but had limited long-term clinical benefit.[7] Some serious side effects of long term administration included sustained ventricular tachycardia resulting in circulatory collapse, worsening myocardial ischemia, acute myocardial infarction, and worsening congestive heart failure.[7][11] Amrinone has good absorption from the gastrointestinal tract [12] and has led to gastrointestinal upset when taken orally. The oral form of the drug is no longer in use.[11] Currently, only acute intravenous administration takes place.[11] The effects of amrinone vary widely with species and experimental condition; therefore, its inotropic effects are variable.[3] A loss in sensitivity to phosphodiesterase 3 inhibitors, including amrinone, has been observed in end stage heart failure in humans; other treatment options may be more useful for improvement in these stages.[3]

Naming

Amrinone is the INN, while inamrinone is the United States Adopted Name, which was adopted in 2000 in an attempt to avoid confusion with amiodarone.[13]

Synthesis
Amrinone synthesis:[14][15][16][17]

See also: Milrinone and Pelrinone.

References
  1. Hamada Y, Kawachi K, Yamamoto T, et al. (August 1999). "Effects of single administration of a phosphodiesterase III inhibitor during cardiopulmonary bypass: comparison of milrinone and amrinone". Japanese Circulation Journal. 63 (8): 605–9. doi:10.1253/jcj.63.605. PMID 10478810.
  2. Klein N.A.; Siskind S.J.; Frishman W.H.; Sonnelblick E.H.; LeJemtel T.H. (1981). "Hemodynamic Comparison of Intravenous Amrinone and Dobutamine in Patients With Chronic Congestive Heart Failure". American Journal of Cardiology. 48 (1): 170–175. doi:10.1016/0002-9149(81)90587-7. PMID 7246440.
  3. Xiong W.; Ferrier G.R.; Howlett S.E. (2004). "Diminished Inotropic Response to Amrinone in Ventricular Myocytes from Myopathic Hamsters Is Linked to Depression of High-Gain Ca2+-Induced Ca2+ Release". The Journal of Pharmacology and Experimental Therapeutics. 310 (2): 761–773. doi:10.1124/jpet.103.064873. PMID 15064331. S2CID 6036283.
  4. Wilmshurst P. "The HealthWatch Award 2003: Dr Peter Wilmshurst - "Obstacles to honesty in medical research"". Archived from the original on 2015-04-25. {{cite journal}}: Cite journal requires |journal= (help)
  5. Levy J.H.; Ramsay J.; Bailey J.M. (1990). "Levy J.H., Ramsay J., Bailey J.M.". Journal of Cardiothoracic Anesthesia (4): 7–11. doi:10.1016/0888-6296(90)90226-6.
  6. LeJemtel T.H.; Scortichini D.; Levitt B.; Sonnenblick E.H. (1989). "Effects of Phosphodiesterase Inhibition on Skeletal Muscle Vasculature". American Journal of Cardiology. 3 (2): 27–30. doi:10.1016/0002-9149(89)90389-5. PMID 2909994.
  7. Packer M.; Medina N.; Yushak M. (1984). "Hemodynamic and clinical limitations of long- term inotropic therapy with amrinone in patients with severe chronic heart failure". Circulation. 70 (6): 1038–1047. doi:10.1161/01.cir.70.6.1038. PMID 6388899.
  8. Carabello B.A. (1980). "Effects of Amrinone on Myocardial Energy Metabolism and Hemodynamics in Patients with Severe Congestive Heart Failure Due to Coronary Artery Disease". Circulation. 62 (1): 28–34. doi:10.1161/01.cir.62.1.28. PMID 7379283.
  9. Konstam M.A.; Cohen S.R.; Weiland D.S.; Martin T.T.; Das D.; Isner J.M.; Salem D.N. (1986). "Relative Contribution of Inotropic and Vasodilator Effects of Amrinone- induced Hemodynamic improvement in congestive heart failure". American Journal of Cardiology. 57 (4): 242–248. doi:10.1016/0002-9149(86)90899-4. PMID 3004184.
  10. LeJemtel T.H.; Keung E.; Ribner H.S.; Davis R.; Wexler J.; Blaufox D.M.; Sonnenblick E.H. (1980). "Sustained Beneficial Effects of Oral Amrinone on Cardiac and Renal Function in Patients With Severe Congestive Heart Failure". American Journal of Cardiology. 45 (45): 123–129. doi:10.1016/0002-9149(80)90229-5. PMID 7350759.
  11. Rettig G.; Sen S.; Frohlig G.; Schieffer H.; Bette L. (1986). "Withdrawal of long-term amrinone therapy in patients with congestive heart failure: a placebo controlled trial". European Heart Journal. 7 (7): 628–631. doi:10.1093/oxfordjournals.eurheartj.a062114. PMID 3530768.
  12. Alousi A.A.; Farah A.E.; Lesher G.Y.; Opalka C.J. (1979). "Cardiotonic Activity of Amrinone- Win 40680 [5-Amino-3, 4- bipyridin- 6(1H)-one]". Circulation. 45 (5): 666–677. doi:10.1161/01.RES.45.5.666. PMID 39684.
  13. "Amrinone Becomes Inamrinone". USP Quality Review. United States Pharmacopeia. 73. March 2000. Archived from the original on 2008-10-03.
  14. G. Y. Lesher, Ch. J. Opalka, U.S. Patent 4,004,012 (1977).
  15. Ch. J. Opalka, G. Y. Lesher, U.S. Patent 4,072,746 (1978).
  16. G. Y. Lesher, C. J. Opalka, U.S. Patent 4,107,315
  17. GB 2070008, Gelotte, Karl Olaf & Parady, Edward David, "Process for preparing 5-cyano(3,4'-bipyridin)-6(1H)-one", published 1981-09-03, assigned to Sterling Drum Inc.
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