Adrenergic preparations
ά2 β2 β1 ά1 CОМТ МАО
Localization of alfa-adrenoceptors
Localization of alfa-adrenoceptors
Localization of beta-adrenoceptors
Localization of beta2-adrenoceptors
Localization of beta3-adrenoceptors β3-adrenoceptors are located in the cells of fatty tissue, in the mast cells and in pancreatic β-cells. Their excitation leads correspondingly to increase of lipolysis, to inhibition of mast cell degranulation and to stimulation of insulin release.
Excitation: Of α-receptors causes the increasing of functions (tone of smooth muscles) except intestine and uterus Of β- receptors – decreasing of functions (tone of smooth muscles) except heart
Adrenomimetics Directly acting – Adrenalini hydrochloridum – α1 α2 β1 β2 β3 -Noradrenalini hydrotartras – α1 α2 β1 - Mesatonum - α1 -Isadrinum - β1 β2 -Dobutamine - β1 -Salbutamolum - β2 Fenoterolum - β2 Indirect action – - Ephedrini hydrochloridum α1 α2 β1 β2 β3
The main effects of adrenaline the increase of automatism (heart rate), excitability, conduction and contractility (cardiac output) of myocardium the increase of the arterial pressure, hyperglycemia, dilation of bronchi, dilation of pupils inhibition of mast cell degranulation increase of oxygen demand and production of energy.
The main effects of noradrenaline acts predominantly upon the cardiovascular system – increases the arterial pressure (both systolic and diastolic one) The rapid increase of arterial pressure stimulates a reflex reaction from vascular mechanoceptors that leads to the development of sinus bradycardia introduced only intravenously because in subcutaneous or intramuscular introduction it causes strong local vasospasm that may be accompanied by development of necrosis.
Ephedrini hydrochloridum Acts upon the presynaptic membrane and stimulates noradrenaline release from the sympathetic nerve endings. It also slightly excites the adrenoceptors located on the postsynaptic membrane. The same effects as Adrenaline, but it's less active (in 50-100 times), action develops gradually and lasts longer stimulates the CNS, may cause psychomotor excitement, insomnia and euphoria (drug dependence). In the repeated introduction of ephedrine within small interval (10-30 mm.) the tachyphylaxis appears
Ephedra
Indications for use- Adrenaline anaphylactic shock and some other allergic reactions, bronchial asthma, acute hypotension (collaps), hypoglycemic coma, cardiac arrest, depression of excitability and conduction of myocardium, for extension of local anesthetics' action. Locally- in open angle glaucoma, for the arrest of capillary hemorrhage Adrenaline is used only by parenteral way or locally because its destroyed in oral introduction.
Mesatonum increases BP -indicated in collaps
Indications for use- Isadrinum - indicated in bronchial asthma, atrioventricular blockade, bradycardia. Salbutamol, fenoterol - bronchial asthma, premature or precipitated labor Dobutamine - acute heart failure which accompanies the myocardial infarction.
Alpha-Adrenergic Blockers Type of blockade Tropaphenum – non-competitive; slow onset and long duration. 2-stage blockade. All the rest: competitive Selectivity Nonselective: Tropaphenum and phentolamine alpha-1 selective: Prazosin, terazosin, others alpha-2 selective: Yohimbine alpha/beta blockers: Labetalol Others: phenothiazines, tricyclic antidepressants
Pharmacological Effects Eye - miosis GI tract – Increased motility Urinary bladder – decreased tone in sphincter Metabolic effects – increased insulin secretion
Imidazoline derivatives - phentolamine Many other effects including: Parasympathomimetic Increased gastric acid secretion Cardiac stimulation Increased secretion from exocrine glands, such as salivary, sweat, lacrimal, pancreatic Coronary artery disease and peptic ulcer relative contraindication to it.
Alpha-1 selective blockers Prazosin Less cardiac stimulation since it preserves alpha-2 mediated negative feedback + other mechanisms Used in congestive heart failure and in hypertension but tolerance develops with time, maybe due to fluid retention. Adverse effects: First dose phenomenon. Favorable effect on plasma lipids: increase HDL/LDL ratio
Pharmacological Properties Propranolol Cardiovascular Blood pressure, heart rate, cardiac output, peripheral vascular resistance, coronary and organ blood flows Pulmonary Central Nervous System Metabolic
Antihypertensive Effect of Beta-Blockers Mechanisms 1. Decreased cardiac output 2. Inhibition of renin-angiotensin system 3. Decreased central sympathetic outflow 4. Resetting of baroreceptor 5. Others: prejunctional receptors, prostaglandins, etc.
Beta-Blockers - Adverse Effects Cardiac (mechanical; electrical) Vascular (decreased perfusion) Pulmonary (bronchocostriction) Metabolic (diabetes mellitus) Central Nervous System (depression, nightmares, etc.) Withdrawal Syndrome