Pharmacology Made Simple

Pharmacology: Three Types

  1. Systemic Pharmacology:
    • Focuses on the study of drugs that affect the entire body through the bloodstream, often targeting multiple organs and systems.
  2. Ans Pharmacology (Autonomic Nervous System):
    • Cholinergic:
      • Agonists: Drugs that mimic the action of acetylcholine (e.g., muscarinic agonists).
      • Antagonists: Drugs that block acetylcholine receptors (e.g., atropine).
    • Adrenergic:
      • Agonists: Drugs that stimulate adrenergic receptors (e.g., beta-agonists).
      • Antagonists: Drugs that block adrenergic receptors (e.g., beta-blockers).
  3. Antimicrobial Pharmacology:
    • Focuses on drugs that are used to treat infections by targeting microorganisms like bacteria, viruses, fungi, and parasites.
Three types of pharmacology: systemic, autonomic nervous system, and antimicrobial pharmacology with focus areas.

1. CVS Pharmacology – Anti-Hypertensive (Anti-HTN)

  1. ACE Inhibitors (pril):
    • Side Effects: Dry cough, angioedema
    • Contraindication: Not to be used in pregnancy
  2. Spironolactone:
    • Side Effects: Gynecomastia, hyperkalemia
  3. Hydralazine:
    • Side Effect: Drug-induced lupus erythematosus (SLE)
  4. Alpha-Methyl Dopa:
    • Safe for use during pregnancy
  5. Procainamide
  6. Isoniazid
CVS pharmacology antihypertensives: ACE inhibitors, spironolactone, hydralazine, alpha-methyl dopa, procainamide with uses and side effects
  1. Labetalol
  2. Carvedilol
  3. Short-acting Intraoperatively:
    • Esmolol
  4. Dyslipidemia
    • Metoprolol
  5. Digoxin:
    • Action: Inhibits the Na+/K+ pump
    • Effect: Leads to increased potassium levels and increased contractility of the heart.
Gestational hypertension drugs: labetalol, carvedilol, esmolol, metoprolol and digoxin with key actions.

3. Lipid-Lowering Agents

  1. Statins:
    • MOA: Inhibit HMG-CoA reductase
    • Side Effects (S/E):
      • Hepatotoxicity
      • Rhabdomyolysis
      • Combined with fibrates: Increased risk of gallstones
  2. Niacin (Vitamin B3):
    • MOA: Inhibits liver production of VLDL (very low-density lipoproteins), leading to a reduction in triglycerides and LDL cholesterol.
    • Effect: Increases HDL cholesterol (good cholesterol).
    • Side Effects (S/E):
      • Flushing (due to vasodilation)
      • Hepatotoxicity (in high doses)
      • Hyperglycemia (can worsen diabetes)
Lipid-lowering drugs: statins and niacin with mechanisms, effects, and side effects.

4. Antiarrhythmic Medications

  1. Na Channel Blockers:
    • Class 1a:
      • Quinidine: Causes cinchonism (ringing in the ears, vertigo, headache)
      • Procainamide: Can cause SLE (Systemic Lupus Erythematosus)
      • Disopyramide: Can lead to heart failure (HF) edema
    • Class 1b:
      • Lidocaine: Used as a local anesthetic
      • Phenytoin: Used for epilepsy, can cause gingival hyperplasia
    • Class 1c:
      • Propafenone: Contraindicated after MI (heart attack)
  2. K Channel Blockers:
    • Amiodarone: Used for AIDS treatment, has various arrhythmic indications
    • Ibutilide: Used for atrial arrhythmias
  3. Ca Channel Blockers:
    • Diltiazem
    • Verapamil
Table of antiarrhythmic drugs with classes, uses, and side effects including sodium, potassium, and calcium channel blockers.

5. Thyroid Drugs

  1. Hyperthyroidism:
    • PTU (Propylthiouracil): Preferred in 1st trimester of pregnancy
    • Methimazole: Used after the 1st trimester of pregnancy
  2. Hypothyroidism:
    • Levothyroxine (synthetic T4)

6. Diabetes Mellitus (DM)

  1. Insulin:
    • Side Effects (S/E):
      • Hypoglycemia
      • Lipodystrophy
  2. Oral Agents
    • Biguanides:
      • Metformin: First-line for DM2 (especially with obesity)
      • Contraindicated in renal failure
  3. Sulfonylureas:
    • Glyburide, Tolbutamide
    • Side Effects (S/E):
      • Hypoglycemia
      • Weight gain
  4. Thiazolidinediones (TZDs):
    • Pioglitazone: Can increase DM2 risk and risk of fractures
  5. SGLT2 Inhibitors:
    • Empagliflozin
    • Dapagliflozin
    • Increase glucose excretion in urine, leading to reduced blood glucose levels.
Diabetes mellitus drugs table including insulin, metformin, sulfonylureas, TZDs, and SGLT2 inhibitors with mechanisms and side effects.

7. GIT

Acid Suppression Therapy

  1. Proton Pump Inhibitors (PPI):
    • Used for: Zollinger-Ellison syndrome
  2. H2 Blockers:
    • Cimetidine:
      • Side Effect (S/E): Gynecomastia
  3. Prostaglandin Analogues:
    • Misoprostol:
      • Used for NSAID-induced gastric ulcers
  4. Antacids:
    • Aluminum Hydroxide:
      • Side Effect (S/E): Constipation
  5. Magnesium Hydroxide:
    • Side Effect (S/E): Diarrhea
GIT pharmacology drugs table with PPIs, H2 blockers, misoprostol, and antacids with side effects.

8. Antiemetic Medications

  1. Ondansetron:
    • MOA: 5HT3 receptor inhibitor
    • Effect: Decreases vomiting and reduces chemotherapy-induced vomiting.
  2. Metoclopramide:
    • MOA: Inhibits dopamine receptors in the chemoreceptor trigger zone
    • Side Effects: Parkinson-like symptoms
    • Use: In diabetic gastroparesis
  3. Aprepitant:
    • MOA: Acts on NK-1 receptor (neurokinin)
    • Used to control nausea and vomiting, especially related to chemotherapy.
  4. Domperidone:
    • MOA: Dopamine antagonist, used to treat nausea and vomiting.
Antiemetic drugs table with ondansetron, metoclopramide, aprepitant, and domperidone with MOA and uses.

Here are other materials for NLE NRE step 1

9. Laxatives

  • Lactulose:
    • Use: Also used in hepatic encephalopathy to reduce ammonia levels in the blood.

10. Antidiarrheal Medications

  • Metronidazole:
    • Use: Primarily an antibiotic, used for infections such as Clostridium difficile or giardiasis. It is not a typical antidiarrheal, but it can help treat infections that cause diarrhea.
  • Loperamide:
    • Use: A common antidiarrheal that works by slowing down gut motility, helping reduce the frequency of diarrhea.
Antidiarrheal medications table showing metronidazole and loperamide with uses.

11. Parasympathetic vs Sympathetic Nervous System

FeatureParasympatheticSympathetic
Preganglionic FibersLong and attach near target organShort, and postganglionic fibers are long
Postganglionic FibersShort, attach to M1, M2, M3 receptorsLong
NeurotransmitterAcetylcholine (ACh)Norepinephrine (NE) and Epinephrine (Epi), except in sweat glands (ACh)
Cranial Nerves InvolvedCN 3, CN 7, CN 9, CN 10N/A
ReceptorsM1, M2, M3 receptorsM3 receptors in adrenal medulla

12. Acetylcholine (ACh) Receptors

Table summarizing cholinergic receptors: Nn in ganglia/adrenal medulla, Nm in neuromuscular junction, M1 excitatory in CNS/stomach, M2 inhibitory in heart, M3 excitatory in smooth muscle/glands/eye, M4 and M5 inhibitory in brain
Receptor TypeLocation
Nn (Nicotine)Autonomic ganglia, adrenal medulla
Nm (Nicotine)Neuromuscular junction of skeletal muscle
M1Activates in certain tissues
M2Inhibits (primarily in heart tissue)
M3Activates in various organs (e.g., smooth muscle)
M4, M5Inhibitory effects, specific areas of brain

13. Micturition Control

SympatheticParasympatheticMedicationsEffect
Alpha 1, Beta 3M3Bethanechol (Muscarinic Agonist)Void increases (promotes urination)
Hypogastric NerveActivated by BethanecholOxybutynin (Muscarinic Antagonist)Decreases urgency incontinence and detrusor overactivity (relieves urgency)
Effect: Increase urinary retentionMirabegron (Sympathomimetic)Increases bladder capacity (used for urgency incontinence)
Tamsulosin (Alpha Blocker)Reduces urinary obstruction (used for BPH – benign prostatic hyperplasia)
Muscarinic Agonist: BethanecholIncreases bladder emptying, urinary retention relief
Acetylcholine receptor types table showing Nn, Nm, M1, M2, M3, M4, M5 with locations.

Receptors & Effects:

ReceptorEffect
Alpha 1Vasoconstriction, smooth muscle contraction
Alpha 2Inhibition
Beta 1Increased heart rate (HR)
Beta 2Bronchodilation
Beta 3Increased lipolysis, bladder relaxation
Adrenergic receptors table with alpha and beta subtypes and their effects on heart, lungs, vessels, and bladder

Check your NRE Step 1 result after completing the exam.

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