Atenolol 712313 225616887 2008-07-14T16:01:12Z AkhtaBot 6756213 robot Adding: [[ar:دواء أتنولول]] <references/>{{drugbox | |image=Atenolol.png |IUPAC_name = 2-(4-(2-hydroxy-3-(isopropylamino)propoxy)phenyl)acetamide |CAS_number = 29122-68-7 | ATC_prefix=C07 | ATC_suffix=AB03 | PubChem=2249 | DrugBank=APRD00172 | C=14 | H=22 | N=2 | O=3 | molecular_weight = 266.336 g/mol | smiles = OC(CNC(C)C)COc1ccc(cc1)CC(=O)N | bioavailability = 40-50% | protein_bound = 6-16% | metabolism = [[Liver|Hepatic]] <10% | elimination_half-life = 6-7hours | excretion = [[Kidney|Renal]]<br>[[Mammary gland|Lactic]] (In lactiferous females) | pregnancy_AU = C | pregnancy_US = D | pregnancy_category = | legal_status = Rx-only | routes_of_administration = Oral or [[Intravenous|IV]] }} '''Atenolol''' is a [[beta-1 receptor|β<sub>1</sub> receptor]] specific antagonist, a drug belonging to the group of [[beta blocker|β-blockers]], a class of drugs used primarily in [[cardiovascular disease]]s. Introduced in [[1976]], atenolol was developed as a replacement for [[propranolol]] in the treatment of [[hypertension]]. The chemical works by slowing down the heart and reducing its workload. There is no evidence to suggest that it is addictive.<ref name="WuA">{{cite journal |author=Wu A |title=Should beta-blockers still be used as initial antihypertensive agents in uncomplicated hypertension? |journal=Ann. Acad. Med. Singap. |volume=36 |issue=11 |pages=962–4 |year=2007 |month=November |pmid=18071610 |doi= |url=http://www.annals.edu.sg/pdf/36VolNo11Nov2007/V36N11p962.pdf |issn= |accessdate=2008-05-19}}</ref> Unlike [[Propranolol]], atenolol does not pass through the blood-brain barrier thus avoiding various CNS side effects.<ref name="BBB">{{cite journal |author=Agon P, Goethals P, Van Haver D, Kaufman JM |title=Permeability of the blood-brain barrier for atenolol studied by positron emission tomography |journal=J. Pharm. Pharmacol. |volume=43 |issue=8 |pages=597–600 |year=1991 |month=August |pmid=1681079 |doi= |url= |issn= |accessdate=2008-05-19}}</ref> Whilst atenolol, the most widely used β-blocker in the [[United Kingdom]], was once first-line treatment for [[hypertension]], the role for β-blockers in hypertension was downgraded in June 2006 in the United Kingdom to fourth-line as they perform less well than other drugs, particularly in the elderly, and there is increasing evidence that the most frequently used β-blockers at usual doses carry an unacceptable risk of provoking [[Diabetes mellitus type 2|type 2 diabetes]].<ref name="NHSnews">{{cite web | author= Sheetal Ladva | title=NICE and BHS launch updated hypertension guideline | url=http://www.nelm.nhs.uk/Record%20Viewing/viewRecord.aspx?id=567178 | date=2006-06-28 | publisher=[[National Institute for Health and Clinical Excellence]] | accessdate=}}</ref> ==Indications== Atenolol (trade name Tenormin) can be used to treat cardiovascular diseases and conditions such as [[hypertension]], [[coronary heart disease]], [[arrhythmia]]s, [[angina]] (chest pain) and to treat and reduce the risk of heart complications following [[myocardial infarction]] (heart attack) Due to its hydrophilic properties, the drug is less suitable in [[migraine]] prophylaxis compared to propranolol, because for this indication, atenolol would have to reach the brain in high concentrations, which is not the case (see below). Atenolol is a so-called β<sub>1</sub>-selective (or 'cardioselective') drug. That means that it exerts greater blocking activity on myocardial β<sub>1</sub>-receptors than on β<sub>2</sub> ones in the lung. The β<sub>2</sub> receptors are responsible to keep the bronchial system open. If these receptors are blocked, bronchospasm with serious lack of oxygen in the body can result. However, due to its cardioselective properties, the risk of bronchospastic reactions if using atenolol is reduced compared to nonselective drugs as [[propranolol]]. Nonetheless, this reaction may also be encountered with atenolol, particularly with high doses. Extreme caution should be exerted if atenolol is given to [[asthmatic|asthma]] patients, who are particularly at risk; the dose should be as low as possible. If an asthma attack occurs, the inhalation of a β<sub>2</sub>-mimetic antiasthmatic, such as [[hexoprenaline]] or [[salbutamol]], will usually suppress the symptoms. Provisional data suggests that antihypertensive therapy with atenolol provides weaker protective action against cardiovascular complications (e.g. myocardial infarction and [[stroke]]) compared to other antihypertensive drugs. In particular, [[diuretic]]s are superior. However, controlled studies are lacking.<ref name="pmid15530629">{{cite journal |author=Carlberg B, Samuelsson O, Lindholm LH |title=Atenolol in hypertension: is it a wise choice? |journal=Lancet |volume=364 |issue=9446 |pages=1684–9 |year=2004 |pmid=15530629 |doi=10.1016/S0140-6736(04)17355-8}}</ref> Unlike most other commonly-used β-blockers, atenolol is excreted almost exclusively by the [[kidney]]s. This makes it attractive for use in individuals with end-stage [[liver]] disease. ==Pharmacokinetic data== *t<sub>cmax</sub> = 2 to 4 hours after oral dosing (time elapsed before maximal concentration in the [[blood plasma]] is reached) *The mean elimination [[halflife]] is 6 hours. However, the action of the usual oral dose of 25 to 100 mg lasts over a period of 24 hours. *Atenolol is a [[hydrophilic]] drug. The concentration found in brain tissue is approximately 15% of the plasma concentration only. The drug crosses the [[placenta]] barrier freely. In the milk of [[breastfeeding]] mothers, approximately 3 times the plasma concentrations are measured. *Atenolol is almost exclusively eliminated [[Kidney|renally]] and is well removable by [[dialysis]]. A compromised [[liver]] function does not lead to higher peak-activity and/or a longer halflife with possible accumulation. However, preexisting renal insufficience of higher degree makes dose-reductions necessary (see below) ==Contraindications== *[[bradycardia]] (pulse less than 50 bpm) *cardiogenic shock *[[asthma]] (may cause broncho-constriction), although unlikely as atenolol is cardioselective *symptomatic hypotension (blood pressure of less than 100/60 mm Hg with dizziness, vertigo etc.) *angina of the Prinzmetal type (vasospastic angina) *metabolic acidosis (a severe condition with a more acid blood than normal) *severe disorders in peripheral arterial circulation *AV-Blockage of second and third degree (a particular form of [[arrhythmia]]) *acutely decompensated congestive heart failure (symptoms may be fluid retention with peripheral [[edema]] and/or abdominal fluid retention (ascites), and/or lung edema) *[[sick sinus syndrome]] (a particular form of arrhythmia, very rarely encountered) *hypersensitivity and/or [[allergy]] to atenolol *[[phaeochromocytoma]] (a rare type of tumor above the kidneys) Caution: patients with preexisting asthma bronchiale Caution: only if clearly needed during [[pregnancy]], as atenolol may retard fetal growth and possibly causes other abnormalities. (If you are pregnant or plan to become pregnant, ask your doctor.) ==Side effects== {{seealso|Propranolol}} Atenolol causes significantly fewer central nervous system side effects (depressions, nightmares) and fewer bronchospastic reactions, both due to its particular pharmacologic profile. It was the main β-blocker identified as carrying a higher risk of provoking [[Diabetes mellitus type 2|type 2 diabetes]], leading to its downgrading in the United Kingdom in June 2006 to fourth-line agent in the management of hypertension.<ref name="NHSnews"/> In addition, β-blockers blunt the usual sympathetic nervous system response to hypoglycemia (i.e. sweating, agitation, tachycardia). These drugs therefore have an ability to mask a dangerously low blood sugar, which further decreases their safety and utility in diabetic patients. Side effects include: *[[indigestion]], [[constipation]] *dry mouth *fatigue or dizziness (especially cases of [[orthostatic hypotension]]) *hair loss *problems with sexual function *runny/blocked nose *depression and confusion *difficulty sleeping, nightmares *weakness or lack of energy These side effects may or may not be experienced, but if they are, you should notify your doctor. More serious side effects can include: *[[hallucinations]] *low blood pressure ([[hypotension]]) *skin reactions, eg. [[rash]], hives, flaking of skin, worsening of [[psoriasis]] *sensation of '[[pins and needles]]' hands or feet *irritated eyes, visual disturbances *difficulty hearing *difficulty speaking *unsteadiness when walking These side effects can be serious and may indicate urgent medical attention is necessary. All of these side effects are very rare, and others not mentioned in the above list can occur in some people. ==Interactions== {{seealso|Propranolol}} ==Dosage== In patients with normal renal function, the daily dose is 25 to 50 [[milligram|mg]] for the management of hypertension depending on the indication and severity of the disease. In most patients, the physician will start with a low initial dose and make increments in weekly intervals as tolerated. Dosage can vary from as little as 25 mg to 200mg a day. In cases of doses over 100mg, the dosage is usually divided and taken twice daily. For the management of angina, 100mg daily may be given. In patients with impaired renal function the daily dose should be reduced according to the clinical response of the individual patient. If a patient with end-stage renal failure is scheduled on regular dialysis, usually 50 mg are given after each dialysis procedure. In these patients, a severe hypotension may occur afterwards. ==Combination treatment of hypertension== If atenolol alone fails to control arterial hypertension, the drug can be combined with a diuretic (e.g. with [[chlortalidone]] in [[co-tenidone]]) and/or a vasodilator ([[hydralazine]], or in severe cases [[minoxidil]]). Central alpha-agonists (e.g. [[clonidine]]), [[ACE Inhibitor]]s or [[Angiotensin II receptor antagonist]]s such as losartan can also be given additionally. Exert caution with calcium-antagonists of the [[verapamil]]-type as adjunct therapy because of additional negative impact on the muscular strength of the heart. Use of calcium-antagonists of the [[nifedipine]]-type is controversial. ==Overdose== Symptoms of [[overdose]] are due to excessive pharmacodynamic actions on β<sub>1</sub> and also β<sub>2</sub>-receptors. These include [[bradycardia]], severe [[hypotension]] with [[Shock (medical)|shock]], acute [[heart failure]], [[hypoglycemia]] and bronchospastic reactions. Treatment is largely symptomatic. Hospitalization and intensive monitoring is indicated. In early cases emesis can be induced. [[Activated charcoal]] is useful to absorb the drug. [[Atropine]] will counteract bradycardia, [[glucagon]] helps with hypoglycemia, [[dobutamine]] can be given against hypotension and the inhalation of a β<sub>2</sub>-mimetic as [[hexoprenalin]] or [[salbutamol]] will terminate bronchospasms. ==References== {{reflist|2}} *{{cite book |title=Patient Information Leaflet — Atenolol tablets BP |year=2003 |publisher=CP Pharmaceuticals Limited}} ==External links== *[http://www.atenolol.tk/ Atenolol], [http://www.chm.bris.ac.uk/motm/motm.htm Molecule of the Month] (uses [[Macromedia Flash]]). *[http://www.sunderland.ac.uk/~hs0dad/profile/atenolol/atenhmpg.htm Atenolol drug information] {{beta blockers}} [[Category:Beta blockers]] [[Category:Amides]] [[ar:دواء أتنولول]] [[de:Atenolol]] [[es:Atenolol]] [[fr:Atenolol]] [[hr:Atenolol]] [[it:Atenololo]] [[hu:Atenolol]] [[pl:Atenolol]] [[pt:Atenolol]] [[ru:Атенолол]] [[uk:Атенолол]] [[zh:阿替洛尔]]