NEET MDS Synopsis
CHOLINERGIC DRUGS
Pharmacology
CHOLINERGIC DRUGS
Produce actions similar to Acetylcholine (Ach)
Cholinergic Agonists
1 Acetylcholine 2 Methacholine 3. Carbachol 4 Bethnechol
Alkaloids
1.Muscarine 2 Pilocarpine 3. Arecoline
MECHANISM OF ACTION
I Heart- hyperpolarizes the SA node and decreases the rate of diastolic depolarisation. thus the frequcncy of impulse generation is decreased. bradycardia.
2 Blood vessels- vasodilatation
3. Smooth muscles - increased contraction. increased tone. increased peristalsis.
4. Glands- increased sweating. increased lacrimation.
5 Eye- contraction of the circular muscle of iris (miosis).
Nicotinic action
Autonomic ganglia - stimu1ation of sympathetic and parasympathetic system.
Skeletalmuscles - contraction of fibres.
CNS..No effect as it does not penetrate the blood-brain barrier.
Toxic effects
Flushing. sweating.salivation. cramps. belching. involuntary mictuirition. defaccation.
Contraindication
1.. Anginapectoris- decreases the coronary flow.
2 Pepticulcer - increases the gastric secretion
3 Asthma- bronchoconstriction
4 Hyperthyroidisim
Cholinomimetic Alkaloids
Pilocarpine
Prominent muscarinic actions. causes marked sweating. salivation. Increase of secretions. small doses cause fall in BP but higher doses increase in BP. Applied to the eye cause miosis. fall in intraocular tension
Uses
I. .Open angle glaucoma
2. To counteract mydriasis
Anticholinesterase
They inhibit the enzyme cholinestrase and prolong the action of Ach
Reversible
Physostigamine, Ncostigamine, Pyridostigamine, Ambenonium, Edrophonium, Demecarium
Irreverible
Dyflos. Echothiphate.
Pharmacological Actions
I Ganglia - persistent depolarisation of ganglionic nicotinic receptors.
2 CVS - unprcdictable as Muscarinic-I receptor causes bradycardia but ganglionic stimulation
tachycardia.
3. Skeletal muscles - as Ach is not destroyed and rebinds to the same receptor or it diffuses on to the neighbouring receptors to cause repetitive firing. twitching and fasciculations.
Uses
I As miotic
a) Glaucoma : Acute congestive (narrow angle) glaucoma, Chronic simple (wide angle) glaucoma
b) Counter act atropine mydriasis.
2) Post operative paralytic ileus
3) Myasthenia gravis
4) Postoperativedecurarization
5) Cobra bite
6) Belladona poisoning
7) Other drug overdoses
Origins of Craniofacial muscles
Anatomy
Mesodermal Origin
Muscles
Innervation
Somitomeres 1, 2
Superior, medial and ventral recti
Oculomotor (III)
Somitomere 3
Superior oblique
Trochlear (IV)
Somitomere 4
Jaw-closing muscles
Trigeminal (V)
Somitomere 5
Lateral rectus
Abducens (VI)
Somitomere 6
Jaw-opening and other 2nd arch muscles
Facial (VII)
Somitomere 7
Stylopharyngeus
Glossopharyngeal (IX)
Somites 1, 2
Intrinsic laryngeals
Vagus (X)
Somites 2-5
Tongue muscles
Hypoglossal (XII)
Nystatin
Pharmacology
Nystatin
Candida spp. are sensitive to nystatin.
Uses: Cutaneous, vaginal, mucosal and esophageal infections.
Candida infections can be treated with nystatin.
Cryptococcus is also sensitive to nystatin.
Nystatin is often used as prophylaxis in patients who are at risk for fungal infections, such as AIDS patients with a low CD4+ count and patients receiving chemotherapy.
MOA
nystatin binds to ergosterol, the main component of the fungal cell membrane. When present in sufficient concentrations, it forms a pore in the membrane that leads to K+ leakage and death of the fungus.
Meperidine
Pharmacology
Meperidine (Demerol)
Meperidine is a phenylpiperidine and has a number of congeners. It is mostly effective in the CNS and bowel
Produces analgesia, sedation, euphoria and respiratory depression.
Less potent than morphine, 80-100 mg meperidine equals 10 mg morphine.
Shorter duration of action than morphine (2-4 hrs).
Meperidine has greater excitatory activity than does morphine and toxicity may lead to convulsions.
Meperidine appears to have some atropine-like activity.
Does not constrict the pupils to the same extent as morphine.
Does not cause as much constipation as morphine.
Spasmogenic effect on GI and biliary tract smooth muscle is less pronounced than that produced by morphine.
Not an effective antitussive agent.
In contrast to morphine, meperidine increases the force of oxytocin-induced contractions of the uterus.
Often the drug of choice during delivery due to its lack of inhibitory effect on uterine contractions and its relatively short duration of action.
It has serotonergic activity when combined with monoamine oxidase inhibitors, which can produce serotonin toxicity (clonus, hyperreflexia, hyperthermia, and agitation)
Adverse reactions to Meperidine
• Generally resemble a combination of opiate and atropine-like effects.
- respiratory depression, - tremors, - delirium and possible convulsions, - dry mouth
• The presentation of mixed symptoms (stupor and convulsions) is quite common in addicts taking large doses of meperidine.
Cell Functions
General Microbiology
Cell Functions:
-> Autolysis
- degradative reactions in cells caused by indigenous intracellular enzymes – usually occurs after cell death
- Irreversible (along with Coagulative necrosis or infarcts) – reversible: fatty degeneration, & hydropic degeneration
-> Autolysin:
• Ab causing cellular lysis in the presence of complement
• Autolytic enzymes produced by the organism degrade the cell’s own cell wall structures
-> In the presence of cephalosporins & penicillins, growing bacterial cells lyse
• W/o functional cell wall structures, the bacterial cell bursts
-> Heterolysis: cellular degradation by enzymes derived from sources extrinsic to the cell (e.g., bacteria)
-> Necrosis: sum of intracellular degradative reactions occurring after individual cell death w/in a living organism
Ketoprofen
Pharmacology
Ketoprofen
It acts by inhibiting the body's production of prostaglandin.
Oxycodone
Pharmacology
Oxycodone
About equal potency to morphine. Very effective orally.
It is combined with aspirin or acetaminophen for the treatment of moderate pain and is available orally
Oxycodone is a semisynthetic compound derived from thebaine, with agonist activity primarily at mu receptors.
CENTRAL NERVOUS SYSTEM PHARMACOLOGY
Pharmacology
CENTRAL NERVOUS SYSTEM PHARMACOLOGY
Antipsychotic Drugs
1. Phenothiazines
a. Aliphatic derivatives
(1) Chlorpromaxine
b. Piperidine derivatives
(1) Thioridazine
(2) Mesoridazine
c. Piperazine derivatives
(1) Fluphenazine
(2) Perphenazine
(3) Prochlorperazine
(4) Trifluoperazine
2. Haloperidol resembles the piperazine phenothiazines.
3. Thiothixene resembles the piperazine phenothiazines.
4. Others (e.g., loxapine, pimozide).
5. Newer and more atypical antipsychotic drugs:
a. Clozapine
b. Olanzapine
c. Quetiapine
d. Risperidone
e. Ziprasidone
f. Aripiprazole
Antidepressant Drugs
Drug treatment of depression is based on increasing serotonin (5-HT) or NE (or both) at synapses in selective tracts in the brain. This can be accomplished by different mechanisms.
Treatment takes several weeks to reach full clinical efficacy.
1. Tricyclic antidepressants (TCAs)
a. Amitriptyline
b. Desipramine
c. Doxepin
d. Imipramine
e. Protriptyline
2. Selective serotonin reuptake inhibitors (SSRIs)
a. Fluoxetine
b. Paroxetine
c. Sertraline
d. Fluvoxamine
e. Citalopram
3. Monoamine oxidase inhibitors (MAOIs)
a. Tranylcypromine
b. Phenelzine
4. Miscellaneous antidepressants
a. Bupropion
b. Maprotiline
c. Mirtazapine
d. Trazodone
e. St. John’s Wort
Antimania Drugs
These drugs are used to treat manic-depressive illness.
A. Drugs
1. Lithium
2. Carbamazepine
3. Valproic acid
Sedative Hypnotics
1. Benzodiazepines
2. Barbiturates
3. Zolpidem and zaleplon
4. Chloral hydrate
5. Buspirone
6. Other sedatives (e.g., mephenesin, meprobamate, methocarbamol, carisoprodol, cyclobenzaprine)
7. Baclofen
8. Antihistamines (e.g., diphenhydramine)
9. Ethyl alcohol
Antiepileptic Drugs
Phenytoin
Carbamazepine
Phenobarbital
Primidone
Gabapentin
Valproic acid
Ethosuximide
Anti-Parkinson Drugs
a. L-dopa plus carbidopa (Sinemet).
b. Bromocriptine, pergolide, pramipexole, ropinirole.
c. Benztropine, trihexyphenidyl, biperiden, procyclidine.
d. Diphenhydramine.
e. Amantadine.
f. Tolcapone and entacapone.
g. Selegiline.