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100 Cards in this Set

  • Front
  • Back

Neurons

Sensory-toward CNS


Associative-between neurons


Motor-away from CNS

Parts of the neuron

Cell body.


Dendrite-impulse toward cell body


Axon-impulse away cell body

Two parts of the nervous system

CNS-central


PNS-peripheral

CNS

Brain and spinal cord.


Interpret impulses and send signals to PNS.


May increase or block activity.

PNS

12 cranial nerves.


Paired spinal nerves (Dorsal roots-sensory in, Ventral roots-motor out)


Autonomic nervous system (involuntary)

Autonomic nervous system

Sympathetic-adrenergic


Parasympathetic-cholinergic

Sympathetic

"fight or flight"-increases heart rate, etc.


Short preganglionic fibers, AcetylCholine neurotransmitter.


Long postganglionic fibers, epinephrine or norepinephrine.


Arise from thoracic and lumbar regions.

Effects of Anticholinergic Drugs: "EAD"


Cardiac:

Increases heart rate

"EAD"


Vascular

Causes vasoconstriction to digestive organs and skin and vasodilation to skeletal muscles.

"EAD"


Bronchi

Dilates bronchi and decreases bronchial secretions.

"EAD"


Gastointestinal

Relaxes smooth muscle tone of the GI tract, decreases GI motility and peristalsis, and decreases GI secretions.

"EAD"


Urinary

Relaxes urinary bladder muscles, increases constriction of the internal sphincter muscle of the urinary bladder, and causes urine retention.

"EAD"


Ocular

Causes mydriasis (pupillary dilation) and paralyzes the ciliary muscle.

"EAD"


CNS/Muscular system

Decreases muscle rigidity and can cause drowsiness and disorientation.

"EAD"


Glandular

Decreases salivation, perspiration, and tear production.

alpha 1

Effect-increases force of heart contraction, increases blood pressure, and causes mydriasis.



Blocking-Vasodilation and miosis

alpha 2

Effect-Inhibits release of norepinephrine and dilates blood vessels, producing hypotension



Blocking-None

beta 1

Effect-Increases heart rate and force of heart contraction



Blocking-decreases heart rate

beta 2

Effect-Dilates bronchioles and relaxes GI tract.



Blocking-Constricts bronchioles

Parasympathetic

"homeostatic". Normal heart rate, etc.


ACh released at both pre and postganglionic synapse. Long pre, short post fibers.


Fibers found in brain stem and sacral nerves.

Effects of Cholinergic Drugs: "ECD"


Cardiac

Decreases heart rate and slows conduction of the AV node.

"ECD"


Vascular

Causes vasodilation (lowers blood pressure)

"ECD"


Bronchi

Stimulates bronchial smooth muscle contraction and increases bronchial secretions.

"ECD"


GI

Increases motility of the smooth muscles of the stomach, increases peristalsis, and relaxes sphincter muscles.

"ECD"


Urinary

Contracts urinary bladder muscles, relaxes sphincter muscles of the urinary bladder, and stimulates urination.

"ECD"


Ocular

Causes miosis (pupillary constriction)

"ECD"


Skeletal muscle

Maintains muscle strength and tone

"ECD"


Glandular

Increases salivation, perspiration, and tear production.

Seizures

Periods of altered brain function due to recurrent abnormal electrical impulses in cerebral cortex

Anticonvulsants

Help prevent seizures by suppressing the spread of abnormal electric impulses from the seizure focus to other areas of the cerebral cortex.



All anticonvulsants are CNS depressants- May cause ataxia, drowsiness, and hepatotoxicity.

Anticonvulsant Catergories

Barbiturates-CNS depressants (phenobarbital)


Benzodiazepines-potentiate GABA (diazepam, Valium)


Potassium Bromide (KBr)-Chloride competitor


Phenytoin (Dilantin)-side effects limit use in animals


Add ons-used in small animals with refractory seizures uncontrolled by standard drugs

Barbiturates

Derivative of barbituric acid. Grouped by duration of action.


Long acting (6-8 hrs)-phenobarbital


Short acting (1-2 hrs)-pentobarbital


Ultrashort-(10-15 min)-thiopental, methohexital

Phenobarbital (oral-Primidone)

Long acting, anticonvulsant of choice in dogs and cats. C-IV controlled, IV or PO.


May cause liver enzymes (SAP, ALT) to rise, animal may develop tolerance.


Should take periodic blood samples for signs of liver damage.

Pentobarbital

Short acting, administered IV, C-11 controlled substance.


Commonly used as an euthanasia solution.

Thiopental

Ultra short. Administered IV for induction of anesthesia prior to intubation or for short procedures.

Benzodiazepines

Potentiate effects of GABA.


Used IV for status epilepticus.


diazepam (Valium), iorazepam (Ativan), clorazepate

GABA

Inhibitory neurotransmitter that stabilizes nerve cell membrane.

Potassium bromide (KBr)

Hyperpolarizes membrane, raises seizure threshold and limits spread of seizures. Long half life (24 days) takes several days to reach therapeutic range.

Add-Ons

Used for refractory seizures.

Add-On-levetiracetam (Kappra)

Dogs and cats with refractory epilepsy.


Binds to synaptic vesicle protein.


Side effects include sedation, ataxia, and anorexia.

Add-On-zonisamide (Zonagran)

Blocks calcium and sodium channels in the brain.


Facilitates serotonin and dopamine.


Side effects include ataxia and sedation.

Add-on-gabapentin (Neurontin)

Inhibits calcium channels resulting in decreased excitatory neurotransmission.


Side effects-sedation, ataxia, and potential hepatotoxicity.

Add-on-felbamate (Felbatol)

Used in dogs to control seizures by potentiating GABA and inhibiting calcium channels.


Side effects-hepatotoxicty, reversible blood dyscrasias, and keratoconjunctvitis sicca.

Calming Agents

Tranquilizers, Sedatives, Anti-anxiety drugs

Phenothiazines (acepromazine)

Sedation, antianxiety, antiemetic, antiarrhythmic, antihistamine effect, peripheral vasodilation, seizure threshold reducer.

Butyrophenones (Not in U.S.)

Sedation, Antiemetic

Benzodiazepines (Valium, Telazol)

Antianxiety, Muscle relaxant. No analgesia. Used with ketamine or tiletamine for short-term anesthesia.

Alpha 2 Agonists (Xylazine)

Sedation, Analgesic, Muscle relaxant, Emetic.


Premedicate with atropine (anticholinergic)


xylazine (Rompun)- most common


detomidine (Dormosedan)- used for colic in horses.


Domitor & Dexdomitor-sedation and analgesia in dogs. IM or IV. Reversed with atipamezole, (Antisedan)

Phenothiazine derivatives

Causes sedation, relieves fear and anxiety.


acepromazine-(Promace)


chlorpromazine-(Thorzine)


compazine


promazine-(Sparine)

xylazine (Rompum)

Combined with ketamine for short term procedures. Emetic. Can be reversed with yohimbine or tolazoline.


IMPORTANT: Always check Rompum label for dosage concentration. Large animal is 100mg/ml, small is 20.

Analgesia (Pain Relief)


Classified as:

Physiologic: the bodies protective mechanism to avoid tissue injury.



Pathologic: arises from tissue injury and inflammation or from damage to nervous system.

Analgesia can be further divided into:

Nociceptive: transient pain due to peripheral tissue injury.



Neuropathic: damage to the peripheral nerves or central nervous system.



acute/chronic

Nociceptive pain

Somatic Pain-arises from joint, bone, muscle, skin, or connective tissue.



Visceral Pain-arises from visceral organs

Neuropathic Pain

Centrally generated pain-peripheral or central nervous system injury. Dysregulation of the ANS



Peripherally Generated Pain-Peripheral nerve injury.

Nociceptive Pain Pathway

Transduction-Stimulus to electrical energy


Transmission-Through PNS to spinal cord, brain


Modulation-What CNS does with pain signal


Perception-Awareness

Signs of pain

abnormal, licking, biting, changes, etc.

Analgesics

Non or narcotic.


Preemptively-before pain starts


Multimodally-combining drugs from different classes to achieve synergism.

Narcotics

Refers to opiate (natural from opium poppy seeds) or opioid-like (synthetic). Work on CNS.

Non-Narcotics

Used for mild to moderate pain, are non-addictive, and work on the PNS receptors.

Opoids

Do not produce anesthesia. Produce analgesia and sedation, and relieve anxiety.


Described by their action at the opioid receptor.


Side effects: respiratory depression, excitement if given too rapidly.

Mu

Found in the pain area of the brain and spinal cord.

Kappa

Found in the cerebral cortex and spinal cord

Delta

Found in the brain, spinal cord, provide minimal analgesia in animals.

Affinity

Drug's ability to bind with a receptor.


Affects a drug POTENCY.

Activity

Ability of drug to cause action in or on receptor cell.

Based on affinity and activity, opioids are:

Full agonists-bind to receptor & produce effect.


Partial agonists-potent activity


Full antagonists- No activity


Partial antagonists-reversal agents

Opioids

Opium, Morphine sulfate, hydromorphone, butorphanol, hydrocodone, fentanyl, etorphine, buprenorphine, pentazocine, methadone, codeine, tramadol, diphenoxylate, loperamide, apomorphine.

Opium

C-lll, paregoric in tincture. Natural opioid, antidiarrheal in calves and foals.

Morphine sulfate

C-ll, inject or oral. Naturally occurring, affects mu and kappa receptors. Treats severe pain, preanesthetic, anesthetic, emetic

Hydromorphone

(Dilaudid) IV, IM, SQ pre-op. Semisynthetic mu agonist, C-ll, 5x more potent than morphine, also treats severe post-op pain

Butorphanol

(Torbugesic) (Torbutrol) C-lV. Synthetic opioid, 2-5x analgesia of morphine. Potent antitussive, analgesic, preanesthetic. Comes in small animal and horse concentrations.

Fentanyl

(Duragesic). Transdermal, IV, tablet. Synthetic, transdermal patch, C-ll, 200x morphine

Etorphine

(M-99) for immobilization of zoo and exotic animals, C-ll, 1000x morpine

Tramadol

(Ultram) Centrally acting opioid agonist with mu receptor activity, SSRI. Used to control chronic pain, for oral analgesia and antitussive.

Loperamide

(Immodium) antidiarrheal

Opioid Antagonists

Blockers. Used to treat respiratory and CNS depression. Naloxone. Naltrexone

Naloxone

a opioid antagonist used to reverse respiratory depression following narcotic overdose, given IV, IM, SQ

Naltrexone

used to treat behavior disorders and chronic licking

Neuroleptanalgesics

combination of an opioid and a tranquilizer or sedative to relieve pain and calm anxiety. No longer available commercially.

Anesthetics

Anesthesia- means without sensation- NO PAIN

Local Anesthetics

Block pain at site.


Examples: lidocaine, proparacaine, tetracaine, mepivacaine, bupivacaine.

Types of Local Anesthesia

Infiltration, Topical, Nerve block, Line block, Regional (epidural)

Injectable general anesthetics (1)

Barbiturates: CNS depressants derived from barbituric acid. Used mainly as anticonvulsants, anesthetics, and euthanasia solutions.


Side effects: potent cardiovascular and respiratory depression.

Injectable general anesthetics (2)

Dissociatives: belong to the cyclohexamine family (PCP, angel dust)


Examples: ketamine and tiletamine.

Misc. Injectable general anesthetics

-Guaifenesin: Skeletal muscle relaxant used in combo with an anesthetic drug to induce general anesthesia in horses.


-Propofol: short acting inj. anesthetic agent that produces rapid and smooth induction when given IV.-Side effects-cardiac arrhythmias and apnea. Hypnotic agent.

Inhalant General Anesthetics

"Volatile anesthetics"


Compared on value called MAC-minimum alveolar concentration. Measure of the strength of anesthetic.


Lower MAC= More potent (halothane)


Higher MAC= Less potent (isofluorane)

Blood-to-gas solubility

Hi BGS= longer induction, longer recovery


Low BGS= faster induction and recovery

Methods of Administering Anesthetics by Inhalation

Open-drop, semi-closed, closed

Inhalant general anesthetics (1)

Halothane (Fluothane). Nonflammable, inhalant anesthetic administered via a precision vaporizer. Leave animals on 100% oxygen following surgery to prevent diffusion hypoxia.

Inhalant general anesthetics (2)

Isoflurane (Isoflo). Nonflammable, inhalant anesthetic administered via a precision vaporizer.


Side effects include respiratory depression and malignant hyperthermia.

Inhalant general anesthetics (3)

Isomers of isoflurane. Nonflammable and have fewer cardiovascular side effects than other inhalants. C-sections.


Examples: Enflurane, Desflurane, Sevoflurane-side effect profound respiratory depressant, close monitoring needed.

Inhalant general anesthetics (4)

Sevoflurane: produces rapid induction and rapid recoveries. Produce fewer cardiovascular side effects. Has low tissue solubility, resulting in rapid elimination of the drug by the body.

CNS Stimulants

Reverse CNS depression caused by CNS depressants.


Doxapram: (Dopram V)-C-sections, sublingual drop or via umbilical cord.


Methylxanthines: bronchodilators. Include caffeine, theophylline, and aminophylline. Considered performance-enhancing

Euthanasia Solutions

Used to humanely end an animal's life. When pentobarbital is in combo with other agents, it is a C-lll controlled substance (Beuthanasia-D)

ANS drugs

Autonomic nervous system drugs work either by acting like neurotransmitters or by interfering with neurotransmitter release.

Two groups of drugs affect the parasympathetic nervous system

Cholinergics (parasympathomimetics)-mimic the action of the parasympathetic nervous system.


Anticholinergics (parasympatholytics)

Two groups affect the sympathetic nervous system.

Adrenergics (sympathomimetics)


Adrenergic blockers (sympatholytics)

Anticholinergic Drugs

Inhibit the actions of acetylcholine by occupying the acetylcholine receptors.


Examples:atropine


Used to decrease salvation during anesthesia.

Adrenergic Drugs

Simulate the action of the sympathetic nervous system. Examples: epinephrine, norepinephrine, dobutamine, albuterol.

Adrenergic Blocking Agents

Block the effects of the adrenergic neurotransmitters.


beta-blockers include propranolo, metoprolol, and timolol.