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33 Cards in this Set
- Front
- Back
Tasks of ANS
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-functions of internal organs
- controls internal milieu of the body: chemical (pH, O2, CO2), physical parameters (BP, T) |
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Anatomy of ANS
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-in the periphery the ANS and SNS are almost entirely separated
- in the CNS, the ANS and SNS are intimately connected |
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Sensory input of ANS
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A. mainly interoceptors (pH, O2, etc.)
B. some: special senses and somatic senses |
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effectors of ANS
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1. smooth m.
2. cardiac m. 3. glands |
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sensory input of voluntary NS
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1. special sensory: vision, hearing, taste, smell, equilibrium
2. somatic sensory: pain, touch, pressure, temperature |
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effectors of voluntary NS
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-skeletal muscles = output, voluntary control
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Sympathetic gen
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-fight or flight
- activate resources, stimulate body |
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Parasympathetic gen
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-regeneration
-restores E - vegetative aspects of daily life |
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para vs sympathetic NS
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- many organs are innervated by both, each with a reciprocal effect
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parasympathetic effects
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- constricts pupil
-stim salivation - slows HR - constricts airways - stimulates digestion - contracts ureter - distendes large intestine: increases tonus, relaxes sphincter - contracts bladder, relaxes sphincter - stimulates penile erection |
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sympathetic effects
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-dilates pupils
- inhibits salivation - increases HR - dilates blood vessels - contracts smooth m. - liver: stimulates glucose production and release - pancreas, gall bladder: stimulated release of bile - stimulates sweat glands - adrenal medulla: secretion of epi and norepi - relaxes urinary bladder -stimulates ejaculation |
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parasympathetic division
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CNS--> preganglionic neuron (cholinergic)--> ganglion --> postganglionic neuron (cholinergic)---> effector
-each ganglion has over over 100K neuronal bodies |
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muscarinic cholinergic receptors
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-mimic the effect of ACH
-nicotine has no effect on muscarinic - toadstool (amanita muscaria) |
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nicotinic cholinergic receptors
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- mimic the effect of ACH
- muscarine has no effect on nicotinic receptors - high concentrations of nicotine block the nicotinic receptors (parasympatholytic effect) |
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muscarinic
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-all postganglionic parasympathetic neurons and postganglionic cholinergic sympathetic neurons (smooth m., cardiac m., glands)
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nicotinic
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-all preganglionic sympathetic and parasympathetic neurons and motor endplates(synapses) of skeletal m.
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parasympathomimetic agents
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-mimic the effects of parasympathetic stimulation
-nicotine and muscarine |
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nicotine
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-parasympathomimetic
-LD for men: 1mg/ kg -intoxication: circulatory failure, vomiting, convulsions, respiratory paralysis - therapy: emetica, gastric lavage, artificial respiration, cardio agents, muscle relaxants |
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muscarine
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-no pharmacological importance
-intoxication: salivation, sweating diarrhea, vomiting, miosis( constricted pupils), circulatory failure - antidote: atropine (=parasympatholyticum) |
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parasympatholytic agents
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-reduce or block the effects of parasympathetic stimulation
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atropine
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-parsympatholytic agent
- blocks muscarinic receptors at postanglionic synapses and nicotinic (at high doses only) -pharmacological effect: tachycardia, relaxation of GI, dilation of bronchioles, madra's, anhydrotic effect on glands -clinical uses: preanesthetic prevents bradycardia |
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atropine toxicity
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-considerable interspecies variation
- herbivores generally more resistant: rabbits eat belladonna leaves, horses sensitive -dry mouth, tachycardia, hyperpnoea, ataxia -convulsions and respiratory failure can lead to death |
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Curarine
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-parasympatholytic agent
- prevents the depolarization of postsynaptic membrane of motor endplate (neuromuscular junction) -muscular paralysis -curare: hunting pool of S. American natives - derivatives are peripheral muscle relaxants in IV anesthesia |
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sympathetic division
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CNS -->cholinergic receptor--> ganglion-->adrenergic receptors--> effectors
-ACH: preganglionic transmitter - norepi and acetylcholine: postganglionic transmitter -postgang neurons: sweat glands, piloerector muscles of hair, blood vessels |
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adrenergic receptors
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-bind both epi and norepi
- classified into alpha (1, 2) and beta (1-3) - norepi binds better to alpha receptors (stronger effect) -epi bind better to beta receptors |
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norepi
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-synthesized from the amino acid tyrosine
-stored in vesicles -degraded by mitochondrial monoamine oxidase (MAO) and intracellular (smooth, heart gland) catechol-O-methyltransferase (COMT) |
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effect of norepi on organs
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-alpha receptors
- vessels: constriction (1,2) - bronchi: constriction (1) - fat cells: dec. lipolysis (1,2) - insulin secretion: inhibits (2) - liver: glycogenolysis inc. - renin release: stimulation -GI tract motility: relaxation (2) |
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effect of epi on organs
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-beta receptors
- heart: +chronotropic, dromotropic, inotropic, and bathmorphic -vessels: constriction (2>1) - bronchi: constriction (2>1) - fat cells: lipolysis inc. (2>1) -insulin secretion: stim (2>1) - liver: glycogenolysis inc -renin release: stimulation -GI tract motility: relaxation (2>1) |
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sympathiomimetic agents
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mimic the effects of sympathetic stimulation
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epi
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-sympathiomimetic agent
-adjunvans to local anesthetics -causes constriction of blood vessels which extends the duration of the anesthesia |
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amphetamine
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-sympathiomimetic agent
- stim of CNS: alertness, dec. fatigue - marked peripheral alpha and beta effects (similar to norepi) - effects diminish after repeated application (=tachyphylaxis) despite increase of dose - abuse as a performance enhancer and associated risk of habit formation |
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alpha blockers
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-sympatholytic agents
- clinical use in the treatment of peripheral vasospasm |
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beta blockers
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-sympatholytic agents
- grouped as: 1. selective: mainly 1, 2 or 3 2. non-selective: 1, 2, and 3 -eg beta 1 blockers such as atenolol in heart: prophylaxis of agina pectoris, arrhythmias |