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Class skeletal muscle relaxants
Skeletal muscle relaxants can act peripherally or centrally. Peripherally acting drugs include neuromuscular blockers like non-depolarizing agents (tubocurarine, vecuronium) and depolarizing agents (succinylcholine). Centrally acting drugs include baclofen, diazepam, dantrolene and tizanidine which reduce muscle tone by various mechanisms of action in the spinal cord or brain. The document discusses the classification, mechanisms of action, pharmacokinetics, drug interactions and adverse effects of various skeletal muscle relaxants.
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Class skeletal muscle relaxants
- 1. SKELETAL MUSCLE RELAXANTS DR RAGHUPRASADA MS ASSISTANT PROFESSOR DEPT. OF PHARMACOLOGY SSIMS & RC.
- 2. 210/25/2019 CLASSIFICATION ON BASISOF SITE OF ACTION A) PERIPHERALLY ACTING • NEUROMUSCULAR BLOCKERS • NON DEPOLARIZING AGENTS ACT DIRECTLY -DANTROLINE SODIUM -QUININE • LONG ACTING • TUBOCURARINE PANCURONU IUM • DOXACURIUM PIPECURONIUM INTERMEDIATE ACTING • ATRACURIUM RAPACURONIUM • METOCURINE ROCURONIUM • VECURONIUM SHORT ACTING-MIVACURIUM • DEPOLARIZING AGENTS • SUXAMETHONIUM (SUCCINYLCHOLINE) • DECAMETHONIUM
- 3. 310/25/2019 CENTRALLY ACTING (SPASMOLYTICDRUGS) • MEPHENESIN CONGENERS-MEPHENESIN, CARISOPRODOL, CHLORZOXAZONE, CHLORMEZANONE • BENZODIAZEPINES- DIAZEPAM ( ACT THROUGH GABA A) RECEPTORS) • GABA MIMETIC- BACLOFEN (GABA B) RECEPTORS) THIOCOLCHICOSIDE • DANTROLINE SODIUM ( ACT DIRECTLY BY INTERFERING RELEASE OF CALCIUM FROM SARCOPLASMIC RETICULUM) • THESE DRUGS ARE USED TO CONTROL SPASTIC MUSCLE TONE AS IN EPILESY ,MULTIPLE SCELEROSIS ,CEREBRAL PALSY, STROKE,
- 4. NEUROMUSCULAR JUNCTION •1 CHOLINERGICMOTOR NEURONE, •2 MOTOR END-PLATE, •3 VESICLES, •4 NMR, •5 MITOCHONDRION
- 5. 510/25/2019 DEPOLARIZING AGENTS: SUCCINYLE CHOLINE THESEDRUGS ARE STRUCTURAL ANALOGUE OF ACETYLCHOLINE . AGONIST (DEPOLARIZING) THESE DRUGS ARE USED TO INCREASE THE SAFETY OF GENERAL ANESTHETICS THESE ARE USED PARENTRALLY
- 6. NONDEPOLARIZING BLOCKING DRUGS •PROTOTYPEIS TUBOCURARINE •SURMOUNTABLE BLOCKADE •LOW DOSES ACT AT NICOTINIC RECEPTOR SITE •HIGH DOSES BLOCKADE OF ION CHANNEL PORE
- 7. DEPOLARIZING BLOCKING DRUGS •PHASEI BLOCK ( DEPOLARIZING) • DEPOLARIZATION OF THE END PLATE • CAUSING GENERALIZED DISORGANIZED CONTRACTION OF MUSCLE MOTOR UNIT • FINALLY FLACCID PARALYSIS OCCUR • AUGMENTED BY CHOLINESTERASE INHIBITORS •PHASE II BLOCK ( DESENSITIZING ) • MEMBRANE BECOME REPOLARIZED • DESENSITIZED • MECHANISM IS UNCLEAR CHANNEL BLOCKING IS IMPORTANT • RESEMBLE TO THAT OF NONDEPOLARIZING DRUGS • SURMOUNTABLE BY ACETYL CHOLINESTERASE INHIBITORS
- 8. SKELETAL MUSCLE PARALYSIS•NONDEPOLARIZINGDRUGS •FLACCID PARALYSIS •LARGER MUSCLES ARE MORE RESISTANT AND RECOVER MORE RAPIDLY •DURATION OF ACTION •TIME TO ONSET OF EFFECT •ACT BY BLOCKING ACETYLCHOLINE RECEPTORS. •IN SOME CASES (IN HIGHER DOSES), ACT BY BLOCKING ION CHANNELS. •DEPOLARIZING DRUGS •TRANSIENT FASCICULATIONS FOLLOWED BY FLACCID PARALYSIS •RAPID ONSET AND SHORT DURATION OF ACTION •ACT AS AGONISTS AT ACETYLCHOLINE RECEPTORS
- 9. MECHANISM OF SK.MUSCLE CONTRACTION •INITIATION OF IMPULSE •RELEASE OF ACETYLCHOLINE •ACTIVATION OF NICOTINIC RECEPTOR AT MOTOR END PLATE •OPENING OF ION CHANNEL, PASSAGE OF NA+ , DEPOLARIZATION OF END PLATE •MUSCLE CONTRACTION. •NEUROMUSCULAR BLOCKING AGENTS USED IN CLINICAL PRACTICE INTERFERE WITH THIS PROCESS. •DRUGS, CAN BLOCK NEUROMUSCULAR TRANSMISSION/ OR MUSCLE CONTRACTION BY ACTING
- 10. MECHANISM OF SK.MUSCLE CONTRACTION • PRESYNAPTICALLY: • TO INHIBIT ACETYLCHOLINE SYNTHESIS OR RELEASE (PRACTICALLY NOT USED). • AS THEY MAY HAVE WHOLE BODY UNSPECIFIC NICOTINIC AS WELL AS MUSCARINIC EFFECTS • POSTSYNAPTICALLY: • TO BLOCK THE RECEPTOR ACTIVITY. • TO BLOCK ION CHANNEL AT THE END PLATE • CLINICALLY THESE DRUGS ARE ONLY USED AS AN ADJUVANT TO GENERAL ANESTHESIA, • (ONLY WHEN ARTIFICIAL RESPIRATION IS AVAILABLE.) • THEY INTERFERE WITH THE POST SYNAPTIC ACTION OF • ACETYLCHOLINE.
- 11. MECHANISM OF ACTION (NONDEPOLARIZING AGENTS) • A) AT LOW DOSES: • THESE DRUGS COMBINE WITH NICOTINIC RECEPTORS AND PREVENT ACETYLCHOLINE BINDING.AS THEY COMPETE WITH ACETYCHOLINE FOR RECEPTOR BINDING THEY ARE CALLED COMPETITIVE BLOCKERS • THUS PREVENT DEPOLARIZATION AT END-PLATE. • HENCE INHIBIT MUSCLE CONTRACTION, RELAXATION OF SKELETAL MUSCLE OCCURS • THEIR ACTION CAN BE OVERCOME BY INCREASING CONC. OF ACETYLCHOLINE IN THE SYNAPTIC GAP(BY IHIBITION OF ACETYLE CHOLINE ESTRASE ENZYME) • E.G.: NEOSTIGMINE ,PHYSOSTIGMINE EDROPHONIUM • ANESTHETIST CAN APPLY THIS STRATEGY TO SHORTEN THE DURATION OF BLOCKAGE OR OVER COME THE OVERDOSAGE.
- 12. MECHANISM OF ACTION (NONDEPOLARIZING AGENTS) • AT HIGH DOSES • THESE DRUGS BLOCK ION CHANNELS OF THE END PLATE. • LEADS TO FURTHER WEAKENING OF THE TRANSMISSION AND REDUCES THE ABILITY OF ACH-ESTERASE INHIBITORS TO REVERSE THE ACTION. • ACTIONS • ALL THE MUSCLES ARE NOT EQUALLY SENSITIVE TO BLOCKADE. • SMALL AND RAPIDLY CONTRACTING MUSCLES ARE PARALYZED FIRST. • RESPIRATORY MUSCLES ARE LAST TO BE AFFECTED AND FIRST TO RECOVER.
- 13. PHARMACOKINETICS:• ADMINISTERED INTRAVENOUSLY •CROSS BLOOD BRAIN BARRIER POORLY (THEY ARE POORLY LIPID SOLUBLE) • SOME ARE NOT METABOLIZED IN LIVER, THEIR ACTION IS TERMINATED BY REDISTRIBUTION, EXCRETED SLOWLY AND EXCRETED IN URINE UNCHANGED (TUBOCURARINE, MIVACURIUM, METOCURINE). • THEY HAVE LIMITED VOLUME OF DISTRIBUTION AS THEY ARE HIGHLY IONIZED. • ATRACURIUM IS DEGRADED SPONTANEOUSLY IN PLASMA BY ESTER HYDROLYSIS ,IT RELEASES HISTAMINE AND CAN PRODUCE A FALL IN BLOOD PRESSURE ,FLUSHING AND BRONCHOCONSTRICTION. IS METABOLIZED TO LAUDANOSINE( WHICH CAN PROVOKE SEIZURES),CISATRACURIUM WITH SIMILAR PHARMACOKINETICS IS MORE SAFER. • NON DEPOLARIZERS ARE EXCRETED VIA KIDNEY ,HAVE LONG HALF LIFE AND DURATION OF ACTION THAN THOSE WHICH ARE EXCRETED BY LIVER.
- 14. PHARMACOKINETICS: • SOME (VECURONIUM,ROCURONIUM) ARE ACETYLATED IN LIVER.( THERE CLEARANCE CAN BE PROLONGED IN HEPATIC IMPAIRMENT) • CAN ALSO BE EXCRETED UNCHANGED IN BILE. • THEY DIFFER IN ONSET, DURATION AND RECOVERY (SEE TABLE) • USES: AS ADJUVANT TO ANESTHESIA DURING SURGERY. • CONTROL OF VENTILATION (ENDOTRACHEAL INTUBATION) • TREATMENT OF CONVULSION
- 15. DRUG INTERACTIONS • CHOLINEESTERASE INHIBITORS SUCH AS NEOSTIGMINE, • PYRIDOSTIMINE AND EDROPHONIUM REDUCES OR OVERCOME THEIR ACTIVITY • BUT WITH HIGH DOSES THEY CAN CAUSE DEPOLARIZING BLOCK DUE TO • ELEVATED ACETYLCHOLINE CONCENTRATION AT THE END PLATE. • HALOGENATED HYDROCARBONS ,AMINOGLYCOSIDES , • CALCIUM CHANNEL BLOCKERS SYNERGIZE THEIR EFFECT.
- 16. ADVERSE EFFECTS • FALLIN ARTERIAL PRESSURE CHIEFLY A RESULT TO GANGLION BLOCK , MAY ALSO BE DUE TO HISTAMINE RELEASE THIS MAY GIVE RISE TO BRONCHOSPASM (ESPECIALLY WITH TUBOCURARINE ,MIVACURIUM ,AND ATRACURIUM) • GALLAMINE AND PANCURONIUM BLOCK, MUSCARINIC RECEPTORS ALSO, • PARTICULARLY IN HEART WHICH MAY • RESULTS IN TO TACHYCARDIA.
- 17. DEPOLARIZING AGENTS • DRUGSSUXAMETHONIUM ( SUCCINYLECHOLINE) • DECAMETHONIUM • MECHANISM OF ACTION: • THESE DRUGS ACT LIKE ACETYLCHOLINE BUT PERSIST AT THE SYNAPSE AT HIGH CONCENTRATION AND FOR LONGER DURATION AND CONSTANTLY STIMULATE THE RECEPTOR. • FIRST, OPENING OF THE NA+ CHANNEL OCCURS RESULTING IN DEPOLARIZATION, THIS LEADS TO TRANSIENT TWITCHING OF THE MUSCLE, CONTINUED BINDING OF DRUGS MAKE THE RECEPTOR INCAPABLE TO TRANSMIT THE IMPULSES, PARALYSIS OCCURS. • THE CONTINUED DEPOLARIZATION MAKES THE RECEPTOR INCAPABLE OF TRANSMITTING FURTHER IMPULSES.
- 18. SUCCINYLCHOLINE • IT CAUSESPARALYSIS OF SKELETAL MUSCLE. • SEQUENCE OF PARALYSIS MAY BE DIFFERENT FROM THAT OF NON DEPOLARIZING DRUGS BUT RESPIRATORY MUSCLES ARE PARALYZED LAST • PRODUCES A TRANSIENT TWITCHING OF SKELETAL MUSCLE BEFORE CAUSING BLOCK • IT CAUSES MAINTAINED DEPOLARIZATION AT THE END PLATE, WHICH LEADS TO A LOSS OF ELECTRICAL EXCITABILITY. • IT HAS SHORTER DURATION OF ACTION. • IT STIMULATE GANGLION SYMPATHETIC AND PARA SYMPATHETIC BOTH. • IN LOW DOSE IT PRODUCES NEGATIVE IONOTROPIC AND CHRONOTROPIC EFFECT • IN HIGH DOSE IT PRODUCES POSITIVE IONOTROPIC AND CHRONOTROPIC EFFECT.
- 19. SUCCINYLCHOLINE • IT ACTLIKE ACETYLCHOLINE BUT DIFFUSE SLOWLY TO THE END PLATE AND REMAIN THERE FOR LONG ENOUGH THAT THE DEPOLARIZATION CAUSES LOSS OF ELECTRICAL EXCITABILITY • IF CHOLINESTRASE IS INHIBITED, IT IS POSSIBLE FOR CIRCULATING ACETYLCHOLINE TO REACH A LEVEL SUFFICIENT TO CAUSE DEPOLARIZATION BLOCK. ADVERSE EFFECTS: • BRADYCARDIA PREVENTABLE BY ATROPINE. • HYPERKALEMIA IN PATIENTS WITH TRAUMA OR BURNS • THIS MAY CAUSE DYSRHYTHMIA OR EVEN CARDIAC ARREST. • INCREASE INTRAOCULAR PRESSURE DUE TO CONTRACTURE OF EXTRA OCULAR MUSCLES . • INCREASE INTRAGASTRIC PRESSURE WHICH MAY LEAD TO EMESIS AND ASPIRATION OF GASTRIC CONTENT.
- 20. SUCCINYLCHOLINE PHARMACOKINETICS: • ADMINISTERED INTRAVENOUSLY. •DUE TO RAPID INACTIVATION BY PLASMA CHOLINESTRASE, GIVEN BY CONTINUED INFUSION. THERAPEUTIC USES • WHEN RAPID ENDOTRACHEAL INTUBATIONS IS REQUIRED. • ELECTROCONVULSIVE SHOCK THERAPY.
- 21. MALIGNANT HYPERTHERMIA: • INHERITEDCONDITION PROBABLY CAUSED BY A MUTATION OF CA++ RELEASE CHANNEL OF SARCOPLASMIC RETICULUM, WHICH RESULTS MUSCLE SPASM AND DRAMATIC RISE IN BODY TEMPERATURE. (THIS IS TREATED BY COOLING THE BODY AND ADMINISTRATION OF DANTROLENE) PROLONGED PARALYSIS DUE TO FACTORS WHICH REDUCE THE ACTIVITY OF PLASMA CHOLINESTERASE • GENETIC VARIANTS AS ABNORMAL CHOLINESTERASE, ITS SEVERE DEFICIENCY. • ANTI -CHOLINESTERASE DRUGS, NEONATES, LIVER DISEASE
- 22. DANTROLENE •DIRECTLY ACTING SKELETALMUSCLE RELAXANT •IT REDUCES SKELETAL MUSCLE STRENGTH BY INTERFERING WITH EXCITATION-CONTRACTION COUPLING INTO THE MUSCLE FIBER, BY INHIBITING THE RELEASE OF ACTIVATOR CALCIUM FROM THE SARCOPLASMIC STORES. •IT IS VERY USEFUL IN THE TREATMENT OF MALIGNANT HYPERTHERMIA CAUSED BY DEPOLARIZING RELAXANTS. •THIS DRUG CAN BE ADMINISTERED ORALLY AS WELL AS INTRAVENOUSLY. •ORAL ABSORPTION IS ONLY ONE THIRD. •HALF LIFE OF THE DRUG IS 8-9 HOURS.
- 23. BACLOFEN •IT ACTS THROUGHGABA B RECEPTORS •IT CAUSES HYPER POLARIZATION BY INCREASED K+ CONDUCTANCE REDUCING CALCIUM INFLUX AND REDUCES EXCITATORY TRANSMITTER IN BRAIN AS WELL AS SPINAL CORD •IT ALSO REDUCES PAIN BY INHIBITORY SUBSTANCE ‘P’ IN SPINAL CORD • IT IS LESS SEDATIVE •IT IS RAPIDLY AND COMPLETELY ABSORBED ORALLY, IT HAS A HALF LIFE OF 3- 4 HOURS •IT MAY INCREASES SEIZURES IN EPILEPTICS • IT IS ALSO USEFUL TO PREVENT MIGRAINE •INTRATHECAL ADMINISTRATION EFFECTIVE IN SEVERE SPASTICITY.
- 24. DIAZEPAM • FACILITATING THEACTION OF -AMINOBUTYRIC ACID (GABA) • ACTS AT ALL GABAA SYNAPSES • USEFUL IN MUSCLE SPASMS OF ANY ORIGIN TIZANIDINE • IT IS CONGENER OF CLONIDINE • Α2-ADRENOCEPTOR AGONIST • REINFORCES BOTH PRESYNAPTIC AND POSTSYNAPTIC INHIBITION IN THE CORD AND INHIBITION OF NOCICEPTIVE TRANSMISSION • TOXICITY: DROWSINESS, HYPOTENSION, DRY MOUTH, ASTHENIA • DOSE REQUIREMENT IS VARIES MARKEDLY AMONG PATIENT
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