PHARM 2 Flashcards
The intrinsic property of sarcomere to shorten (actin myosin interaction) and contract is known as (inotropy/ chronotropy)
Inotropy
Chronotropy has a constant flux of parasympathetic and sympathetic tone. With CHF there is more (sympathetic/ parasympathetic)
Sympathetic
What are the two main mechanisms to increase inotropy (contractility)
Increasing the quantity of intracellular calcium
Increasing the sensitivity of contractile proteins to calcium
Combo
All of the following are drugs used in heart disease and failure as positive inotropes. Which are the major drugs used in general practice? A. Dopamine B. Pimobendan C. Digoxin D. Dobutamine E. Milrinone
B
C
Which drugs increase Ca concentration via B adrenergic agonism. They increase cAMP via adenylate cyclase, increasing Ca A. Dopamine B. Pimobendan C. Milrinone D. Dobutamine E. Digoxin
A
D
Phosphodiesterase inhibitors decrease degradation of cAMP, thus increasing Intracellular Ca. Which drugs are these
A. Dopamine B. Pimobendan C. Milrinone D. Dobutamine E. Digoxin
B
C
Pimobendan works by decreasing degradation of cAMP, being a calcium sensitizer (troponin C), and is a phosphodiesterase 3 inhibitor What does phosphodiesterase do
Is in smooth muscle causes vasodilation if arteries and vein
When is pimobendan used
Systolic dysfunction (DCM)
Congestive heart failure
Pre-clinical valve disease with cardiomegaly
Which of the following are contraindications or adverse effects of pimobendan? A. Ventricular hypertrophy B. Sub-aortic stenosis (obstruction) C. Can only be used as a liquid solution D. GIT effects E. Hypotension
A B- don’t use in these C- only pills (incorrect) D- most common SE E. Hypotension may occur as SE
In which of the follow cases can pimobendan be used in cats
A. Hypertrophic Cardiomyopathy (LV hypertrophy)
B. End stage HCM or refractory CHF
C. Dilated and restrictive cardiomyopathy
C is most used
B- can or cannot be used
A- not used
What is digoxin’a primary MOA
Inhibits Na/ K ATPase= increases cellular Na then decreased Na/ Ca exchanger
Which is false regarding digoxin? A. Used in DCM B. Used for atrial fibrillation C. Wide therapeutic window D. Monitored blood concentrations up to 10 days E. Excreted from kidney F. SE include arrhythmias G. Can have digibind (drug Ab)
C- very narrow
What can increase preload
Fluid therapy
High output state (anemia, hyperthyroid)
Heart dz= fluid retention
All of the following are preload reducers (diuretics) Which are used the most for general practice A. Furosemide B. Torsemide C. Bumetanide D. Spironolactone
A
D- K sparing But questionable efficacy in survival
Other 2 are more potent
What increases after load
Hypertension (LV) Vasoconstriction (RAAS and CHF- LV after load) Pulmonary hypertension (RV)
What are 2 prominent drugs used in heart dz and failure to increase forward output
ACE inhibitors (Enalapril (renal) benazepril (renal and hepatic) lisinopril) Amlodipine
Nitrates- nitroglycerin
Pimobendan
Telemisartin
Vasodilators
Ace inhibitors can be used for what
Pre CHF
CHF
Systemic and glomerular hypertension
T/ F ACE inhibitors can cause GIT upset, renal injury (azotemia with furosemide)
True
When would you not want to use ACE inhibitors (contraindication)
Dehydration Azotemia Hyperkalemia Hyponatremia Interacts with NSAID Cisplatin Aminoglycosides
Amlodipine is an after load reducer that can treat
Systemic hypertension
Glomerular hypertension
Vasoconstriction in CHF
T/F. Amlodipine should be used in patients with hypertension that are dehydrated
False- contraindication if dehydrated or hypotension
Can cause GIT upset, hypotension, gingival hyperplasia what resolves with disuse
Nitrates such as Nitroglycerin (increase/ decrease) nitric oxide production
Increase. Is a venodilator
Match 1. Electric depol of ventricle 2. Repol (ventricular recovery) 3. Atrial depol A. P wave B. QRS C. T wave
B
C
A
Antiarrhythmic drugs Class 1 (Na channel block) are associated with atrial and ventricular arrhythmias. Class 1a drugs which decrease upstroke and prolonged AP include _________. Class 1b which shortens AP include _________.
1a- quinidine procainamide
1b- lidocaine mexiletine
T/F lidocaine can cause CNS excitation in both cats and dogs
True. Especially cats
Is class 1b
Cats=1/10 dose (normally prefer ventricular arrhythmias)
Mexiletine is similar
Atenolol can destabilize patients with poor systolic function or poor output. Is to be used with caution or at all with bronchial disease or asthma. What class is it in
2
Sotalol is a class 3 drug with some class 2 effects. T/f
True. It prolongs AP
Diltiazem side effects include
Bradycardia. Hypotension weakness. GIT
What can anti- hemostatic drugs prevent in cats
Feline aortic thromboembolism
Also a tx
Prevents pulmonary thromboembolism from hyper adrenocorticism, IMHA, DIC, nephropathy, HTWM
(Thrombolytics/ anticoagulants/ antithrombotics) interfere with the clotting cascade. (Thrombolytics/ anticoagulants/ antithrombotics) breakdown thrombi that already formed. (Thrombolytics/ anticoagulants/ antithrombotics) interfere with platelet aggregation.
Anticoagulant
Thrombolytics
Antithrombotics
When using heparin as an anticoagulant drug what should be monitored frequently
ACT
aPTT
Acts on antithrombin 3
Low molecular weight heparin needs (less/more) monitoring than unfractionated heparin.
Less- risk for bleeding is less
Aspirin does all of the following except.
A. Reversibly inhibits COX enzymes
B. Causes platelets to not synthesize more COX
C. Blocks TXA2 production for life of platelet
D. Exacerbates GIT or renal dz
A- irreversible
Clopidigreo is a ADP antagonist but cannot bind to the P2Y12 receptor. The platelet activation is inhibited but it is (more/less) effective than aspirin
More. With less side effects
Used in fat cats
What is the MOA of Thrombolytics
Enhance conversion of plasminogen to plasmin
Cleaves fibrin and breaks clot
(Tissue plasminogen activator, urokinase, streptokinase)- used for acute clotting and coronary artery dz. (not for chronic clots)
What drug can be used to block Na/K pump leading to increase of intracellular Ca concentrations?
Digoxin
What are the two types of GI contractions and how long do they last
Phasic- rhythmic. Seconds
Tonic- minutes to hours
What is the largest endocrine organ in the body
GIT
T/F the enteric nervous system can function independently of the CNS
True- affeeent sensory neurons, inter neurons and efferent secretomotor neurons
What is the main neurotransmitter in parasympathetic postganglionic fibers that innervate the SM and secretory cells
Acetylcholine
Also serotonin dopamine vasoactive intestinal peptide ATP nitric oxide
These stimulate motor and secretory activity
Sympathetic (inhibits/ stimulates) motor and secretory activity, and (inhibits/stimulates) sphincter and blood vessel contraction.
Inhibits
Stimulates
What are some gastrointestinal reflexes
Peristalsis Enterogastric reflex (distention of SI suppresses secretion and motor activity of stomach -ENS) Intestino-intestinal (distention of bowel is one segment inhibits activity elsewhere in bowel- ENS)
Postoperative ileus occurs when increased concentrations of circulating ________ from surgical stress cause parasympathetic _______ and thus resection and anastomosis (physical disruption of ENS)
Catecholamines
Hypo-activity ( depression)
What electrolyte imbalances can cause POI
Ca and Mg
What is most of intestine innervated by
Vagus
Prokinetic drugs (similar to parasympathomimetics) increase acetylcholine by
Stimulating release or preventing degradation
Sympathetic NS on the GIT uses what nerve to inhibit contraction and what neurotransmitter
Splanchnic
Norepinephrine
What does lidocaine increase SM contractions?
Duodenum only
What systems are most sensitive to lidocaine toxicosis
Nervous and skeletal
Other species = CV
When is lidocaine contraindicated
Reduced liver function
Low protein
Neonates
Decreased cardiac output
What are some signs of lidocaine toxicity (hours after tx)
Muscle fasciculations
Ataxia
Collapse
Resolve quickly (minutes)
_______ is a muscarinic receptor agonist and mimics the action of acetylcholine. It is also resistant to degradation by acetylcholiesterase. It acts on the duodenum, jenunum, cecum and pelvic flexure
Bethanacol
Cholinergic agents’s primary side effect is
Excessive salivation
Used mainly with gastric and duodenal ulcers
Neostigmine inhibits the activity of what
Acetylcholinesterase- reduces gastric emptying and jejuenal motility Acts in large colon +LC impactions (not for SI ileus or gastric reflux)
Can also be used for foals to pas gas with ab distention
What should be checked before giving neostigmine
If displaced or torsion of colon
Can make impaction colic signs worse
What do 5- hydroxytryptamine receptor agonists bind to and what does that binding cause
Serotonin- 5-HT4
Peristalsis and secretion in myenteric plexus, ileum and pelvic flexure
Metoclopramide stimulates motility by binding to ______ receptors and is an antagonist to _____ receptors (perception of pain and nausea)
5-HT4
5-HT3
Dopamine antagonist too (dopamine inhibits acetylcholine release and reduces SM contraction)
What can metaclopramide not be administered with in the same IV line
Calcium gluconate
Erythromycin
IV CRI to reduce side effects
What are metoclopramide’s side effects and why so we see them?
Extrapyramidal wffects - dopamine inhibition in CNS= sedation and excitement, restless and muscle spasms
What should be given is metoclopramide side effects are seen
Diphenhydramine
Sedatives make it worse!
Coda pride has (less/more) side effects when compared to metaclopramide (also a 5-HT4 agonist and 5-HT3 antagonist)
Less because no anti- dopamine
What do motilin agonists bind to?
Receptors in enteric nerves= release of acetylcholine
Macrolide antibiotics mimic these= motilide
What is the most widely used motilide
Erythromycin
1 for cecal impaction
Stimulates migrating myoelectric complexes
Best IV. Oral = colitis
Where are motilin receptors predominantly found
Duodenum and jejunum (thus erythromycin increased gastric emptying with jejunal contraction)
Also found in pelvic flexure and cecum
Which is true about H2 Antagonists A. Irreversibly bound B. Competitive antagonist C. Highly Bioavailable D. Cimetidine is better than ranitidine
B
A- reversible
C- poor
D- ranitidine> cimetidine (TID) neither great
What do H2 antagonists do
Block gastric and Ach stimulated acid
Some pepsin secretion also inhibited
What is the common denominator for gastric acid secretion regardless of stimulus
Proton pump (H K ATPase pump)
How many days does it take to get a steady state of a proton pump inhibitor
3 (omeprazole)