Department of Pharmacology Centrally active • Baclofen • Benzodiazepines: • Tetrazepam • Diazepam • Clonazepam • Thiocolchicoside • Mephenoxalone • Tizanidine • Guaifenesin • Orphenadrine Peripherally active • Presynaptically active: botulinum toxin • Postsynaptically active: • Depolarizing blocking agents (suxamethonium) • Non-depolarizing blocking agents (atracurium, vecuronium, pancuronium etc.) Mechanism of action • Attenuate transmission of motoric impulses in spinal cord and CNS • Decrease muscle tone, do not influence intentional contractions → weaker muscle relaxant activity • AE: depression of CNS → sedation, somnolence, confusion… • Acute and chronic painful spasms – p.o., parenterally • Spastic rheumatism • Damage of n. ischiadicus (spasms of deep paravertebral muscles, compressions in intervertebral space etc.) • Spastic disorders associated with cerebral palsy, multiple sclerosis, injuries of brain or spine… Mechanism of action: • Increase effects of inhibitory neurotransmitter γ-aminobutyric acid (GABA) in CNS and spine cord Baclofen • Attenuates the activation of motor neurons in the spine cord • GABAB receptor agonist • Multiple sclerosis, cerebral palsy, injuries of brain and spinal cord… • Baclofen • Benzodiazepines: • Tetrazepam • Diazepam • Clonazepam • Thiocolchicoside • Mephenoxalone • Tizanidine • Guaifenesin • Orphenadrine Psychiatric medication with 5 effects: Anxiolytic Hypnotic Muscle relaxant Anticonvulsant Amnestic Low doses have expectorant effect, Higher doses have muscle relaxant and anxiolytic effect MoA: Enhance of GABAergic transmission – GABAA receptors Centrally active • Baclofen • Benzodiazepines: • Tetrazepam • Diazepam • Clonazepam • Thiocolchicoside • Mephenoxalone • Tizanidine • Guaifenesin • Orphenadrine Peripherally active • Presynaptically active: botulinum toxin • Postsynaptically active: • Depolarizing blocking agents (suxamethonium) • Non-depolarizing blocking agents (atracurium, vecuronium, pancuronium etc.) Mechanism of action 1.) Presynaptically active agents – Decrease ACh release – Botulinum toxin 2.) Postsynaptically active agents – Act on nicotinic receptors (NM) • Non-depolarizing • Depolarizing • Firstly described in 15th century by european explorers in S. America • Used by natives as arrow poisons • Tubocurarine – natural alkaloid • Competitive NM receptors antagonists • AE: release of histamine (bronchoconstriction, hypotension, syncope – fainting) • Progressive relaxation: eye muscles → muscles of mastication → neck and limbs → trunk → diaphragm • Administered parenterally • Effect weakens and is reversible – competition of receptors • With long effect (1-2 h): tubocurarine, pancuronium, pipecuronium, vecuronium • With short efect (10-30 min): alcuronium, atracurium • Surgery – muscle relaxation in the operating field, or before mechanical ventilation (tracheal intubation) • Ovedosing: antidote = acetylcholinesterase inhibitors (neostigmine, pyridostigmine…) • NM receptor agonists • Open Na+ channels → cause long-term depolarization → resistancy to activation by ACh = depolarization blockade • Remain on the receptor for a longer time, resistant to AChE • Fasciculation (muscle twitches) → muscle relaxation (paralysis) • AE: cardiac arrhythmias, hyperkalemia, increase of intraocular pressure (IOP) + malignant hyperthermia ! • Decamethonium • Suxamethonium (succinylcholine) • Short-term muscle relaxation (3-5 min) • Mechanical ventilation (tracheal intubation) • Orthopedic manipulations – repositiong of dislocated joint, fractures • Rare AE of depolarizing MR and/or volatile general anesthetics Mechanisms: • Defect of RYR receptor – controls release of Ca2+ from sarcoplasmic reticulum • Increase of Ca2+ in myocyte → uncontrolled increase of contractions, aerobic/anaerobic metabolism • Symptoms: hyperthermia, cramps and rigidity, ↑ heart rate and breathing, cyanosis, lactate acidosis, rhabdomyolysis... • 60 % of untreated cases are lethal (5 % of treated) • Therapy: dantrolene, intensive cooling • Peripherally active muscle relaxant • Blocks the release of Ca2+ from sarcoplasmic reticulum by interaction with RYR • Do not affect smooth muscle and myocardium • Malignant hyperthermia • Spastic disorders associated with spinal cord injury, stroke, cerebral palsy and multiple sclerosis ‒Advantage: no CNS depression