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Drugs Affecting the Cardiovascular System. Ion Channels Blockers Antihypertension Drugs The Treatment of Congestive Heart Failure Antiarrhythmic Drugs Antianginal Drugs Antihyperlipidemic Drugs and Anti-artherosclerosis Drugs. Antihypertensive Drugs. OVERVIEW.

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Drugs Affecting the Cardiovascular System


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    1. Drugs Affecting the Cardiovascular System Ion Channels Blockers Antihypertension Drugs The Treatment of Congestive Heart Failure Antiarrhythmic Drugs Antianginal Drugs Antihyperlipidemic Drugs and Anti-artherosclerosis Drugs

    2. Antihypertensive Drugs OVERVIEW Hypertension is defined as a sustained diastolic blood pressure greater than 90 mmHg (mercury) accompanied by an elevated systolic blood pressure(>140 mmHg). Hypertension results from increased peripheral vascular smooth muscle tone, which leads to increased arteriolar resistance and reduced capacitance of the venous system. Elevated blood pressure is an extremely common disorder, affecting approximately 10-15% of the population. Although many of these individuals have no symptoms, chronic hypertension-either systolic or diastolic can lead to congestive heart failure, myocardial infarction, renal damage, and cerebrovascular accidents. The incidence of morbidity and mortality significantly decreases when hypertension is diagnosed early and is properly treated.

    3. ETIOLOGY OF HYPERTENSION • Essential/primary hypertension:more than 90% of patients have essential hypertension, a disorder of unknown origin affecting the blood pressure-regulating mechanism. • A family history of hypertension in creases the likelihood that an individual will develop hypertensive disease. • Essential hypertension occurs more often among middle-aged males than among middle-aged females. • Environmental factors such as a stressful lifestyle, high dietary intake of sodium, obesity, and smoking all further predispose an individual to the occurrence of hypertension.

    4. ETIOLOGY OF HYPERTENSION Secondary hypertension: occurs in 5-10% of patients. The cause is usually one of the following: • Renal disease which activates the Renin-Angiotensin-Aldosterone System (RAAS) • Endocrine disease, steroid-secreting turmour of the adrenal cortex, adrenaline-secreting tumour of the adrenal medulla.

    5. MECHANISMS FOR CONTROLLING BLOOD PRESSURE • Arterial blood pressure is regulated within a narrow range to provide adequate perfusion of the tissues without causing damage to the vascular system, particularly the arterial intima. Arterial blood pressure is directly proportional to the product of the blood volume, cardiac output and the peripheral vascular resistance. In both normal and hypertensive individuals, blood volume cardiac output and peripheral resistance are controlled mainly by two overlapping control mechanisms: the baroreflexes mediated by the sympathetic nervous system, and therenin-angiotensin-aldosterone system (RAAS). Most antihypertensive drugs lower blood pressure by reducing cardiac output and /or decreasing peripheral resistance.

    6. Classification of Antihypertension: • Sympatholytic drugs • Vasodilators • Inhibitors of RAS • Diuretics

    7. Classification I:Sympatholytic drugs (drugs that alter sympathetic nervous system function)

    8. Classification I:Sympatholytic drugs (drugs that alter sympathetic nervous system function) 1.central antihypertensive drugs Clonidine可乐定, Methyldopa甲基多巴 2.ganglion-blocking agents( ganglionic blocking drugs) Mecamylamine美加明 3.adrenergic neuron blocking agents( antipostganglionic sympathetic neurons) reserpine利血平, guanethidine 胍乙啶

    9. 4.adrenoceptor antagonists (adrenergic receptor blocking agents) ①β-adrenoceptor-blocking agents propranolol普萘洛尔, ②α-adrenoceptor-blocking agents prazosin哌唑嗪 ③αand β-blockers labetalol 拉贝洛尔

    10. Classification II : Vasodilators 1. direct vasodilators • hydralazine 肼苯哒嗪 • sodium nitroprusside 硝普钠 2. calcium channel blockers( calcium antagonists) • nifedipine 硝苯地平 • nitrendipine 尼群地平 3. potassium channel openers • minoxide 米诺地尔(长压定) • diazoxide 二氮嗪 • pinacidil 吡那地尔

    11. Classification III:Inhibitors of RAS 1.angiotensin converting enzyme inhibitors. ACEI • captopril 卡托普利 • enalapril 依那普利 2.angiotensin receptor-blocking agents • losartan 氯沙坦 • valsartan 缬沙坦 3. renin inhibitors: Enalkiren(依那吉仑) , Remikiren(瑞米吉仑)

    12. Classification VI:Diuretics hydrochlorothiazide 氢氯噻嗪 indapamide 吲达帕胺

    13. Classification I. Sympatholytic drugs Subtype 1. Central antihypertensive drugs Normal regulation of blood pressure in CNS: Vasomotor centers Center nervous system controls peripheral sympathetic activity in brain stem • Inhibiting neurons:α2 receptor resulting in blood pressure lowering bradycardia vasodilatation • Exciting neurons: β receptors resulting in blood pressure enhancing tachycardia

    14. Clonidine可乐定 and Methyldopa甲基多巴 may stimulate inhibiting neurons of central adrenoceptors-α2 receptor, resulting in vasodilation, blood pressure lowers.

    15. Drug 1. Clonidine(可乐定) 又称氯压定, 2- imidazoline derivation Pharmacokinetics: • Lipid-soluble, rapid absorption by oral administration • F, 75% t1/2 8~12 hours • 30%~ 50% metabolisms in liver • Others are eliminated unchanged in urine

    16. Mechanism of action: 1.stimulating postsynaptic α2 adrenoceptors in brain stem peripheral sympathetic activity↓  blood pressure↓ producing sedation 2.stimulating Ⅰ1-imidazoline咪唑啉 receptor in rostral ventrolateral medulla oblongata (RVLM延髓腹外侧核吻侧端)peripheral sympathetic activity lowering 3.stimulating opium receptor relieving abstinence syndrome戒断症状

    17. Pharmacodynamics: 1. Relaxation of arterial vessels reduction in peripheral vascular resistance blood pressure↓ lowers 2. Contracting force of cardiac muscule↓ reduction of cardiac output heart rate↓ decreases 3. Decreased renal vascular resistance and maintenance of renal blood flow 4. Inhibiting movement and secretion of gastrointestinal tract  hypertensive patients with ulcer is the better

    18. Adverse reaction: 1.dry mouth/ xerostomia (dry nasal mucosa, dry eyes), nausea, dizziness头晕, sedation嗜睡, parotid gland swelling and pain腮腺肿痛,sleep disturbances with vivid dreams or nightmares噩梦 2.water and sodium (Na+) retention 3.withdrawal syndrome停药反应 headache apprehension(恐惧忧虑), tremors(震颤),abdominal pain, sweating, tachycardia treatment: ①α-adrenergic blocker (phentolamine) ②continuative administration clonidine

    19. Drug 2. Methyldopa 1.center antihypertension drug 2.treatment: mild to moderately severe hypertension with renal failure 3.reducing peripheral vascular resistance, with a variable reduction in heart rate and cardiac output 4.no decreasing renal blood flow and glomerular filtration rate

    20. Clinical uses: 1.moderate hypertensive disease 2.iv drop, therapy of hypertensive crisis高血压危象 3.controlling abstinence syndrome of opium

    21. Subtype 2. ganglion-blocking agents( ganglionic blocking drugs) Drug: Mecamylamine美加明

    22. Subtype 3. Adrenergic neuronblocking agents Drug 1. Reserpine利血平 Pharmacological action: 1. lower blood pressure, with long-term therapy with reserpine cardiac output↓ peripheral vascular resistance↓ heart rate↓ rennin secretion falls↓ salt and water are retained 2. sedative and neuroleptic (精神安定)effect reserpine depletes catecholamine(儿茶酚胺) and 5-hydroxytryptamine (5-HT)

    23. Mechanism of action: • Reserpine can remain bound to amine pump of vesicular membranes in central and peripheral adrenergic neurons for prolonged periods of time. • The storage vesicles are destroyed as a result of their interaction with reserpine and nerve endings lose their ability to concentrate and store norepinephrine and dopamine.

    24. Catecholamines leak into the cytoplasm, where they are destroyed by intraneruronal monoamine oxidase (MAO), depressing the ability to uptake norepinephrine • Reserpine -induced depletion of biogenic amines correlates with evidence of sympathetic dysfunction and antihypertensive effects.

    25. Recovery of sympathetic function requires synthesis of new storage vesicles, which takes days to weeks after discontinuation of the drug, so effect of reserpine is slow and persistent. Clinical uses: • Mild hypertension • Cooperative administration

    26. Adverse effects: Sedation and inability to concentrate or perform complex tasks are the most common adverse effects. More serious is the occasional psychotic depression.

    27. Drug 2. Guanethidine 胍乙啶 Mechanism and sites of action: • Guanethidine inhibits the release of norepinephrine from sympathetic nerve endings. • Guanethidine nerve concentration in transmitter vesicles replaces norepinephrine causes gradual depletion of norepinephrine stores in the nerve ending

    28. Subtype 4. adrenoceptor antagonists (adrenergic receptor blocking agents) ①β-adrenoceptor-blocking agents propranolol普萘洛尔, ②α-adrenoceptor-blocking agents prazosin哌唑嗪 ③αand β-blockers labetalol 拉贝洛尔

    29. Drug1.β-adrenoceptor-blocking agents 1.Mechanism and sites of action ①blocking β-receptor in heart, decreasing cardiac output ②depressing secretion of rennin, inhibiting the rennin-angiotensin-aldosterone system, decreasing level of angiotersin in plasm ③β-blockers may also block β-receptor of presynaptic membrane in peripheral prejunctional to reduce sympathetic vasoconstrictor nerve activity decreasing secretion of norepinephrine ④in never center, affecting sympathetic regulation ⑤changing sensitivity of baroreceptor ⑥increasing synthesis of prostaglandin

    30. Drugs • 普萘洛尔 propranolol β1 β2 • 美托洛尔 metoprolol β1 intrinsic sympathetic mimetic activity • 阿替洛尔 atenolol β1 intrinsic sympathetic mimetic activity

    31. Clinical uses: • Moderate hypertension or severe hypertension of therapeutic ineffective with other antihypertensive drugs. Adverse reaction: • Postural hypotension, dizziness, nausea, vomiting, diarrhea Contraindications: • Severe diseases accompanied heart, brain, kidney, arteriosclerosis, dysfunction of circulation

    32. Drug 2. α1-adrenoceptor-blocking agents 1. Mechanism: 1). blocking selectively postsynaptic α1 receptors in arterioles and venules 2). dilating both resistance and capacitance vessels 2. Drugs: 1). prazosin 哌唑嗪 2). terazosin 特拉唑嗪 3). urapidil 乌拉地尔

    33. Drug 3.α and β adrenoceptor -blocking agents 1.Mechanism: • Blocking α1 and β receptors • Blocking action of β R> blocking action of α1 R 2.Drugs: • labetalol 拉贝洛尔

    34. Classification II. Vasodilators Summary of the Action and Mechanism 1. Dilating directly arterioles but no veins, lowering blood pressure, relaxing smooth muscle of arterioles. 2. Eliciting compensatory responses, mediated by baroreceptors压力感受器 and the sympathetic nervous system, as well as rennin, angiotension and aldosterone opposing the antihypertensive effect of vasodilator such as:tachycardia心动过速; cardiac output↑; plasma rennin activity↑; retention of salt and fluid. 3. Vasodilators are used common by combination with other antihypertensive drugs that oppose the compensatory cardiovascular response.

    35. Subtype1. direct vasodilators Drugs: 1.hydralazine肼屈嗪,肼苯哒嗪 Action: relaxing smooth muscle in arterioles ①via release of nitric oxide (NO) in vascular ②interfere with Ca2+ entering into cell 2.sodium nitroprusside 硝普钠 ①.treating hypertensive emergencies and severe cardiac failure, crisis ②.dilating both arterial and venous vessels decreasing cardiac preload and afteroad

    36. Subtype 2. Calcium channel blockers Action: • Antianginal effects抗心绞痛 • Antiarrhythmic effects抗心律失常 • Dilating peripheral arterioles扩张外周血管Reducing blood pressure Mechanism of action:inhibiting calcium influx into arterial smooth muscle cells

    37. Drugs: 1.Nifedipine硝苯地平,Verapamil维拉帕米,Diltiazem地尔硫卓 2. Dihydropyridine family: • amlodipine, • felodipine, • isradipine, • nicardipine, • nifedipine, • misolipine, ①more selective as vasodilators ②treating selectively angina or coronary spasm ③prolong effect, slow, persist, smoother, reflex sympathetic activation with slight ④antiarteriosclerosis

    38. Subtype 3. potassium channel openers Drugs: • minoxide 米诺地尔(长压定) • diazoxide 二氮嗪 • pinacidil 吡那地尔

    39. Classification III. Inhibitors of RAS NO PGI2

    40. ACEI and AT blocker bradykinin aldosterone

    41. Subtype I. Angiotensin converting enzyme inhibitors ACEI Mechanism of action: 1.inhibiting ACE angiotensinⅠ------angiotensin Ⅱ ↑ ACE ← (-) inhibitors 2.inhibiting RAS( rennin- angiotensin system) in local tissue 3.inhibiting the kalliurein-kini system(激肽释放酶-激肽系统) Drugs: Captopril, 卡托普利

    42. 4.Accelerating release of prostacyclin(PGI2) ↓ vasodilatations ↓ decreased peripheral vascular resistance ↓ decreased blood pressure

    43. 5.accelerating release of nitric oxide (NO) 6.improving myocardial hypertrophy of left ventricle, inhibiting hyperplasia of vascular smooth muscles. decreasing formation of AngⅡ, inhibiting remodeling of myocadia and vascular smooth muscles. 7.cleansing free radical(自由基), protecting tissue ischemia and reperfusion injury 8.affecting metabolism decreasing cholesterol and triglyceride increasing HDL (high density lipoprotein)

    44. Subtype II. Antagonist of Angiotensin II Receptor (Angiotensin II Receptor Blockers Drugs: Losatan 氯沙坦; Valsartan 缬沙坦 Subtype III. renin inhibitors: Drugs: Enalkiren (依那吉仑) , Remikiren (瑞米吉仑)

    45. Classification VI:Diuretics • hydrochlorothiazide 氢氯噻嗪, • indapamide 吲达帕胺

    46. TREANTMENT STRATEGIES Mild hypertension can often be controlled with a single drug. More severe hypertension may require treatment with several drugs that are selected to minimize adverse effects of the combined regimen. Treatment is initiated with any of four drugs depending on the individual patient: a diuretic, a b-blocker, an ACE inhibitor, or a calcium channel blocker. If blood pressure is inadequately controlled, a second drug is added. A b-blocker is usually added if the initial drug was a diuretic, or a diuretic is added if the first drug was a b-blocker. A vasodilator can be added as a third step for those patients who still fail to respond.

    47. Drugs Affecting the Cardiovascular System Antihypertension Drugs The Treatment of Congestive Heart Failure Antiarrhythmic Drugs Antianginal Drugs Ion Channels Blockers Antihyperlipidemic Drugs