Adrenogenic Drug Ans Flashcards

1
Q

What’s the types of alpha Receptors

A

Types is

1-alpha &2-alpha

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2
Q

Mechanism of alpha 1

A

Via ca reales Gq

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3
Q

Alpha one actions?

A
1-vc 
2-GIT SPHINCTER (contracion)
3-radial muscle contraction(Mydrasis)
4-pillomotor  muscle (hair erection)
5-prostatic gland smooth muscle (contraction)
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4
Q

Whats the action of alpha 2

A
Act on inhibition  via Gi
1-presynaptic neuron
Decrease reales of NT
2-pancreatic cell Beta 
(Decrease insulin realse )
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5
Q

What the type of beta receptors

A

B1 and B2and B3

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6
Q

What the action and mechanisms of beta one receptor

A

Act on Gs (⬆️camp)
1-heart muscle (⬆️HR &⬆️CO ⬆️Conductivity)
2-jaxtaglumerolar cell( relasing of renin)

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7
Q

What the mechanisms and action of beta 2

A

Mech. Gs
1-relaxing of smooth muscle of (bronchi and git and ciliary muscle
Uterus )
2-smooth muscle tremor (Vd of arteries of muscle)
3-live (glycogen lysis)
4-mast cell(histamine relase )
5-heart (⬆️Co minor degree of beta one)

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8
Q

Action of beta 3

A

Mech. Gs
Act one adipose tissue (⬆️fatty acid and glycerol )
Because of activation of lipase enzyme

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9
Q

Dopamine receptors

A

D1-D5 Gs act on renal blood flow

D2-3-4 Gi act on presynaptic neuron

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10
Q

What is the direct acting non selective drugs

A
1-epinephrine 
2-nor epinephrine 
3-dopamine 
4-isopropanol 
(dopaxamine).
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11
Q

What’s about epinephrine?

A

ANS Adrenergic Drugs (Sympathetic) A: Adrenergic Agonists 1) Direct-Acting Adrenergic Receptors A: Non-Selective Epinephrine or Adrenaline (EpiPen Epinephrine [ep-i-NEF-rin] is a natural catecholamine Norepinephrine (NE) is methylated to yield epinephrine in the adrenal About medulla which is stored in chromaffin cells theDrug On stimulation, the adrenal medulla releases about 80% epinephrine and 20% norepinephrine directly into the circulation L-isomer is about 20 times more potent than D-isomer.

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12
Q

What’s meaning of up take 1?

A

Norepinephrine trausporter (NET) is transporter protein integrated into the membrane of presynaptiz neurons and it is responsible for reuptake of extracellular monoamine neurotransmitters (NTs) such as norepineplrine. dopamine and serotonin = described as “Uptake one

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13
Q

What’s block up take one

A

Cocaine TRICYCLIC ANTI DEPRESSANT.amphetamiine

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14
Q

What meaning of up take two and inhibitor of it

A
Extraneuronal   monoamine transporter (EMT) is transporter  protein   integrated   into the membrane of postsynaptic neurons. it is responsible for transport monoamine NTs into postsynaptic neurons = described as "Uptake 2 
Inhibit via (cortisone)
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15
Q

What is the pharmaco kinatic of epinephrine?

A

Epinephrine is ineffective orally due to degradation by gut and rapid metabolism by liver: Routes of administration SC VC 5 Slow absorption ? Long duration and less toxicity. MM ? VD = Rapid absorption = Short duration and high toxicity. IV ? in emergency ? rapid onset of action Inhalation ? in bronchial asthma Intracardiac (IC) = in resuscitation Eye drops ? in glaucoma: NB: IV and IC routes are very dangerous (must be diluted to [:10,000). Pharmaco Duration of action kinetic SC (4-6 hours MM (1-4 hours) Inhalation (1-3 hours). Metabolism: Monoamine oxidase Epinephrine Metabolites (MAO) Catechol-O-methyl transferase Epinephrine Metabolites. COMT Norepinephrine and epinephrine metabolites are metanephrine and vanillylmandelic acid which are excreted in urine. VanillyImandelic acid (VMA) excreted in urine (noral adult value E4= Smg in & day = increase VA in urine in patients With pheochromocytoma (tumour in adrenal medulla). Pharma Tube rapid

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16
Q

Which type of epinephrine must dialited

A

Short duration of action and more toxic Iv and IC

Cause VD

17
Q

What’s is the types that must not diluted?

A

Sc because its long duration and low level of toxicity

Cause vc

18
Q

Dignosis of pheochromcytoma

A

Level of veneyl mandlic acid
NORMAL RANGE (4-8mg/day)
When VMA INSCREASED IN URINE SO IT REFERS TO PHEOCHROMOCYTOMA

19
Q

What the side effect of epinephrine

A
Nose(used in epistaxis local and congestion ). 
Effects Skin (Used With local anaesthesia eg Lidocaine VC decrease   absorption?? prolonged the action = decrease toxicity).
20
Q

Pharmacological action??

A

1-Heart (+tve) = inotropic, chronotropic and dromotropic >cardiac output (CO) >Systolic pressure.D 1) Skin. mucous membranes and viscera (a1)VC 5 peripheral resistance (PR)⬆️diastolic pressure:
2) Skeletal muscles (B2): VD+ PR⬇️ diastolic pressure At low doses: B2 effects (vasodilation) OH the vascular system predominate,
whereas at high doses 01 effects (vasoconstriction) are the strongest The cumulative effect is an in systolic blood pressure (B1)and slight + in diastolic pressure (B2)

NB: Epinephrine activates B1 receptors on the kidney 5 reniu release Renin is an enzyme involved in the production of angiotensin II = potent VC

3-Powerful brouchodilatation (B2) It also inhibits the release histamines from mast cells (B2). So it is used in bronchospasm and anaphylactie shock
4-hyperglycemia action via
Glycogenlysis (B2)
Glucagon relase (B2)
Inhibit insulin realse (a2)
5-lipolysis via (B3) 
Activation of lipase enzyme 
Convert lipid to glycerol and FFT
21
Q

What’s the other action of epinephrine?

A

Fascilate NM transmission via (⬆️Ca)increase the ACH FROM motor neuron
Muscle tremor via B2 agonist
Mech. Via increse k in cell and decreased K in serum