Classify the following agonists in terms of the adrenergic receptors they activate and the responses they cause as a result of direct receptor activation: (1) epinephrine, (2) norepinephrine, (3) phenylephrine, (4) isoproterenol, (5) terbutaline, and (6) dobutamine.
| epinephrine | Agonist | alpha receptor. |
| norepinephrine | Agonist | a1 receptor |
| Phenylephrine | Antagonist | a1 receptor |
| Isoproterenol | Agonist | b1 receptors |
| terbutaline | Agonist | b2 receptor |
| dobutamine | Agonist | b1 receptor |
Explain how each of the following affects structures controlled by the sympathetic nervous system, comparing how they work with how a direct-acting agonist such as epinephrine works, and state one or more clinical uses for each: (1) ephedrine, (2) amphetamines, (3) cocaine, and (4) monoamine oxidase (MAO) inhibitors.
(1). Ephedrine: It acts on the alpha-adrenergic agonist and causes vasoconstriction which results in vascular resistance and an increase in blood pressure. It is used in asthma and shock.
(2). Amphetamines: It inhibits the reuptake of monoamine oxidase and thereby terminate the nerve signals. It is used in ADHD, cardiac arrest.
(3). Cocaine: It produces an anesthetic effect by blocking of nerve endings. It has vasoconstrictive effects. It is used for topical or local anesthesia.
(4). MAO inhibitors: Monoamine oxidase inhibitor inhibits the activities of Monoamine Oxidase A and monoamine oxidase B. It makes changes on the chemicals of the brain. It is used in panic disorders, depression.
Recall the sites (effectors) of alpha1-, beta1-, and beta2-adrenergic receptors and state the expected responses from...
Recall the sites (effectors) of alpha1-, beta1-, and beta2-adrenergic receptors and state the expected responses from their activation by a suitable agonist. Explain the difference between direct cardiac (beta1) effects of adrenergic agonists and reflex (baroreceptor reflex–mediated) effects of those same drugs, using norepinephrine, phenylephrine, and isoproterenol as examples. Identify the desired effects when a therapeutic dose of epinephrine is given for anaphylaxis and explain the actions of the drug that earn it the label “drug of choice” for anaphylaxis....
make a outline of the ans system
1. two divisions of ans and alternate terms associated
2. neurotransmitters for each. indicate location Within the
division where NT is released
3. receptor type with main location
4. organ response to stimulation list these specific organs eyes
hear lungs vessels gi tract and bladder then tell which response is
generated in that organ when stimulated
5 . lust drug name which interact with the receptors in each
division including agonist and antagonist...
1. State the responses that a muscarinic agonist would be expected to cause through direct activation of muscarinic cholinergic receptors (consider bethanechol). The student should focus on the main “targets” of parasympathetic nervous system activity: eyes, respiratory system, heart and blood vessels, gastrointestinal (GI) and urinary tracts, and the secretory activity of exocrine glands (e.g., lacrimal, mucous, and so on). 2. List cholinergic responses not normally caused when the usual therapeutic doses of a muscarinic agonist are administered and explain...