أتينولول

أتينولول
البيانات السريرية
الأسماء التجارية	Tenormin, others
AHFS/Drugs.com	Monograph
MedlinePlus	a684031
License data	US DailyMed: Atenolol; US FDA: Atenolol;
فئة السلامة; أثناء الحمل	AU: C ; ;
مسارات; الدواء	By mouth, Intravenous (IV)
فئة الدواء	Selective β1 receptor antagonist
رمز ATC	C07AB03 (WHO) ;
الحالة القانونية
الحالة القانونية	AU: S4 (Prescription only) ; عموماً: ℞ (بوصفة فقط);
بيانات الحركية الدوائية
التوافر الحيوي	40–50%
ارتباط الپروتين	6–16%
الأيض	Liver <10%
Elimination half-life	6–7 hours
الإخراج	Kidney
المعرفات
	IUPAC name (RS)-2-{4-[2-Hydroxy-3-(propan-2-ylamino)propoxy]phenyl}acetamide;
رقم CAS	29122-68-7 ;
PubChem CID	2249;
IUPHAR/BPS	548;
DrugBank	DB00335 ;
ChemSpider	2162 ;
UNII	50VV3VW0TI;
KEGG	D00235 ;
ChEBI	CHEBI:2904 ;
ChEMBL	CHEMBL24 ;
CompTox Dashboard (EPA)	DTXSID2022628 ;
ECHA InfoCard	100.044.941
Chemical and physical data
التركيب	C14H22N2O3
الكتلة المولية	266٫34 g·mol−1
3D model (JSmol)	Interactive image;
Chirality	Racemic mixture
	SMILES O=C(N)Cc1ccc(cc1)OCC(O)CNC(C)C;
	InChI InChI=1S/C14H22N2O3/c1-10(2)16-8-12(17)9-19-13-5-3-11(4-6-13)7-14(15)18/h3-6,10,12,16-17H,7-9H2,1-2H3,(H2,15,18) ; Key:METKIMKYRPQLGS-UHFFFAOYSA-N ;
	(verify)

فادي الحمود

ساهم بشكل رئيسي في تحرير هذا المقال

أتينولول Atenolol (تينورمين) هو مستقبل₁ β antagonist، دواء من مجموعة حاصرات بيتا (وتكتب أحيانا β-blockers)، ويستخدم بصفة أساسية في علاج أمراض القلب والأوعية الدموية. عرف في 1976، وتم تطويره ليحل محل پروپرانولول in the treatment of hypertension. The chemical works by slowing down the heart and reducing its workload. Unlike propranolol, atenolol does not pass through the blood-brain barrier thus avoiding various central nervous system side effects.^[1]

Atenolol is one of the most widely used β-blockers in the المملكة المتحدة and 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 type 2 diabetes.^[2]

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

دواعي الإستعمال

يعطى فمويا ويحقن وريديا ويستخدم في حالات ارتفاع ضغط الدم والذبحة الصدرية وفرط نشاط الغدة الدرقية. Atenolol can be used to treat cardiovascular diseases and conditions such as hypertension, coronary heart disease, arrhythmias, angina (chest pain) and to treat and reduce the risk of heart complications following myocardial infarction (heart attack). It is also used to treat the symptoms of Graves Disease, until antithyroid medication can take effect.

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 β₁-selective (or 'cardioselective') drug. That means that it exerts greater blocking activity on myocardial β₁-receptors than on β₂ ones in the lung. The β₂ receptors are responsible for keeping 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 asthma patients, who are particularly at risk; the dose should be as low as possible. If an asthma attack occurs, the inhalation of a β₂-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 some cases, diuretics are superior. However, controlled studies are lacking.^[3]

Unlike most other commonly-used β-blockers, atenolol is excreted almost exclusively by the kidneys. This makes it attractive for use in individuals with end-stage liver disease.

المعلومات الدوائية

t_cmax = 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 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.

موانع الإستعمال

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 of the adrenal glands)

Caution: patients with preexisting bronchial asthma

Caution: only if clearly needed during pregnancy, as atenolol may retard fetal growth and possibly cause other abnormalities.

الآثار الجانبية

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 type 2 diabetes, leading to its downgrading in the United Kingdom in June 2006 to fourth-line agent in the management of hypertension.^[2]

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.

وتتضمن الآثار الجانبية:

indigestion, constipation
جفاف الفم
dizziness or faintness (especially cases of orthostatic hypotension)
cold extremities
hair loss
problems with sexual function
runny/blocked nose
depression
confusion
difficulty sleeping, nightmares
fatigue, 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

Serious side effects may require urgent medical attention. Some of these side effects are rare and others (not mentioned in the above list) can occur in some people.

التفاعلات

الجرعة

In patients with normal renal function, the daily dose is 25 to 50 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.

مجموعة أدوية ضغط الدم

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 Inhibitors or Angiotensin II receptor antagonists 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..

الجرعة الزائدة

Symptoms of overdose are due to excessive pharmacodynamic actions on β₁ and also β₂-receptors. These include bradycardia, severe hypotension with 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 β₂-mimetic as hexoprenalin or salbutamol will terminate bronchospasms.

انظر أيضا

حاصرات بيتا

المصادر

^ Agon P, Goethals P, Van Haver D, Kaufman JM (1991). "Permeability of the blood-brain barrier for atenolol studied by positron emission tomography". J. Pharm. Pharmacol. 43 (8): 597–600. PMID 1681079. {{cite journal}}: |access-date= requires |url= (help); Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
^ ^أ ^ب Sheetal Ladva (2006-06-30). "Updated NICE guideline on the management of hypertension in adults in primary care". National Institute for Health and Clinical Excellence. Retrieved 2009-02-03.
^ Carlberg B, Samuelsson O, Lindholm LH (2004). "Atenolol in hypertension: is it a wise choice?". Lancet. 364 (9446): 1684–9. doi:10.1016/S0140-6736(04)17355-8. PMID 15530629.{{cite journal}}: CS1 maint: multiple names: authors list (link)

منشورات جامعةدمشق علم تأثير الأدوية.

وصلات خارجية

الكلمات الدالة:

پروپرانولول

[BBB-1] Agon P, Goethals P, Van Haver D, Kaufman JM (1991). "Permeability of the blood-brain barrier for atenolol studied by positron emission tomography". J. Pharm. Pharmacol. 43 (8): 597–600. PMID 1681079. {{cite journal}}: |access-date= requires |url= (help); Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)

[NHSnews-2] أ ^ب Sheetal Ladva (2006-06-30). "Updated NICE guideline on the management of hypertension in adults in primary care". National Institute for Health and Clinical Excellence. Retrieved 2009-02-03.

[pmid15530629-3] Carlberg B, Samuelsson O, Lindholm LH (2004). "Atenolol in hypertension: is it a wise choice?". Lancet. 364 (9446): 1684–9. doi:10.1016/S0140-6736(04)17355-8. PMID 15530629.{{cite journal}}: CS1 maint: multiple names: authors list (link)

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