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PHARMACOLOGY & PHARMACY

Unit 3: Drugs Acting on Peripheral Nervous System

CTEVT Health Science Second Year | Syllabus 2024

GENERAL MEDICINE (H.A) – COMPLETE NOTES

🧠 Introduction to PNS Drugs

Drugs acting on the Peripheral Nervous System (PNS) target nerves outside the brain and spinal cord. This unit focuses on two key classes: Skeletal Muscle Relaxants (which reduce muscle tone and spasm) and Local Anesthetics (which block pain signals in specific areas). Understanding their mechanisms, uses, and adverse effects is crucial for safe clinical practice.

💊 Skeletal Muscle Relaxant Drugs

Definition: Drugs that reduce muscle spasm, stiffness, and pain without causing loss of consciousness. They primarily act centrally (on the CNS).

Tizanidine

Centrally acting α₂-adrenergic agonist
⚙️ Mechanism of Action

Stimulates alpha-2 receptors in spinal cord → decreases release of excitatory neurotransmitters (e.g., glutamate) → reduces muscle tone and spasm.

✅ Uses
  • Muscle spasm (acute/chronic)
  • Spasticity due to stroke, MS, spinal injury
  • Multiple sclerosis-related spasticity
⚠️ Adverse Effects
Drowsiness
Dry mouth
Hypotension
Muscle weakness
Clinical Note: Causes less muscle weakness compared to other muscle relaxants.

Chlorzoxazone

Centrally acting skeletal muscle relaxant
⚙️ Mechanism of Action

Acts at spinal cord level → inhibits polysynaptic reflexes responsible for muscle spasm → reduces pain and stiffness.

✅ Uses
  • Acute musculoskeletal pain
  • Muscle spasm (short-term relief)
  • Painful conditions (e.g., back pain)
⚠️ Adverse Effects
Drowsiness
Dizziness
Nausea
Liver toxicity
Clinical Note: Primarily used for short-term relief (usually ≤2-3 weeks).

📊 Comparison: Tizanidine vs Chlorzoxazone
Feature Tizanidine Chlorzoxazone
Class α₂-agonist Central muscle relaxant
Primary Use Spasticity (chronic) Acute muscle spasm
Key Side Effect Hypotension Hepatotoxicity (rare)
Duration of Therapy Long-term possible Short-term only

🩺 Local Anesthetics

Definition: Drugs that reversibly block pain sensation in a localized area without loss of consciousness.

🔬 Mechanism of Action (CRITICAL)

Block voltage-gated sodium (Na⁺) channels in nerve fibers → prevent depolarization → nerve impulse conduction stops → pain signals do not reach the brain.

Key Point: They bind to the intracellular portion of Na⁺ channels, preventing Na⁺ influx needed for action potentials.

Lignocaine (Lidocaine)

Amide-type local anesthetic
Onset
Fast (2-5 min)
Duration
Moderate (1-2 hr)
✅ Uses
Local infiltration
Dental procedures
Minor surgery
Ventricular arrhythmias
⚠️ Adverse Effects
  • CNS: Dizziness, tremor, seizures (high dose)
  • Cardiac: Depression, bradycardia
  • Allergic reactions (rare)
💡 Did You Know? Lignocaine is also a Class IB antiarrhythmic drug.

Bupivacaine

Amide-type local anesthetic
Onset
Slow (10-20 min)
Duration
Long (4-8 hr)
✅ Uses
Spinal anesthesia
Epidural anesthesia
Nerve blocks
Post-op pain
⚠️ Adverse Effects
  • Cardiotoxicity (ventricular arrhythmias)
  • Hypotension
  • Bradycardia
  • CNS toxicity at high doses
⚠️ Warning: More cardiotoxic than lignocaine. Use with caution in cardiac patients.

📊 Comparison: Lignocaine vs Bupivacaine
Parameter Lignocaine Bupivacaine
Onset Rapid (2-5 min) Slow (10-20 min)
Duration Moderate (1-2 hr) Long (4-8 hr)
Potency Moderate High (4x lignocaine)
Toxicity CNS > Cardiac Cardiac > CNS
Key Use Infiltration, dental, arrhythmias Spinal/epidural, prolonged pain relief

🧠 Memory Aids & Mnemonics

Local Anesthetic Onset

“Lidocaine is Lightning, Bupivacaine is a Breeze”

Lidocaine = Fast onset (Lightning), Bupivacaine = Slow onset (gentle breeze)

Tizanidine Mechanism

“Alpha-2, Relaxes You”

Stimulates alpha-2 receptors → muscle relaxation

Local Anesthetic Toxicity

“Bupivacaine Bothers the Heart”

Bupivacaine has higher cardiotoxicity than lignocaine

📄 ONE PAGE SUMMARY

Skeletal Muscle Relaxants
  • Tizanidine: α₂-agonist, for spasticity, causes hypotension
  • Chlorzoxazone: Central acting, for acute spasm, hepatotoxicity risk
Local Anesthetics
  • Mechanism: Block Na⁺ channels
  • Lignocaine: Fast, moderate duration, for infiltration
  • Bupivacaine: Slow, long duration, cardiotoxic
Key Differences
  • Tizanidine: α₂-agonist vs Chlorzoxazone: central
  • Lignocaine: fast vs Bupivacaine: slow onset
  • Bupivacaine: more cardiotoxic

Download Complete Notes

Get a printable PDF with all drug tables, mechanisms, and exam tips. HA Pharmacology and Pharmacy Unit 3 Drugs Acting on Peripheral Nervous System Notes

HA Pharmacology and Pharmacy Unit 3 Drugs Acting on Peripheral Nervous System NotesHA Pharmacology and Pharmacy Unit 3 Drugs Acting on Peripheral Nervous System Notes

🏷️ Related Topics

Skeletal Muscle Relaxants
Local Anesthetics
Tizanidine
Chlorzoxazone
Lignocaine
Bupivacaine
Pharmacology CTEVT
Na+ Channel Blockers
Muscle Spasm Drugs
Anesthesia Pharmacology
Peripheral Nervous System
Alpha-2 Agonists
Amide Anesthetics
Spasticity Treatment
Nerve Block Drugs
Drug Mechanisms
Adverse Effects
CTEVT Syllabus 2024
Health Science Notes
Medical Pharmacology

© CTEVT Health Science Second Year | Pharmacology Unit 3 Notes – HA Pharmacology and Pharmacy Unit 3 Drugs Acting on Peripheral Nervous System Notes

Source: CTEVT Syllabus 2024 | For academic use only

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