General Anesthetics. General Anesthesia Characteristics. Balanced Anesthesia. Types of General Anesthetics. Four Stages of Anesthesia

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History of Anesthesia General Anesthetics Pharmacology 604 K a t h e r i n e L. N i c h o l s o n, D. V. M., P h. D. Dept. Pharmacology/Toxicology k l n i c h o l @h s c. vcu. edu General Anesthesia Characteristics Definition (G&G) - Reversible depression of CNS function resulting in loss of response to and perception of Balanced Anesthesia Ideal general anesthetic does not exist. Combinations of drugs to accomplish what one anesthetic can not do alone. all external stimuli. - Produce reversible "sleep" Agents used for balanced anesthesia are - - Produce analgesia Hypnotics - Suppress reflexes Neuromuscular blocking agents - Produce muscle relaxation - Produce Amnesia - Do not suppress respiratory and cardiovascular function Analgesics COMBINATION OF DRUGS CAN LOWER DOSES OF EACH DRUG TO PRODUCE THE SAME OR GREATER EFFECT ON PATIENT - Inexpensive and easy to administer Four Stages of Anesthesia Stage I - a n a l g e s i a Stage II - d e l i r i u m Stage III - surgical anesthesia Types of General Anesthetics Extremely diverse group of chemicals which produce a similar endpoint Inhalant or volatile Stage IV - respiratory paralysis Injectable (intravenous) 1

Inhalational Anesthetics Administered as vapors or gases Special set of physical principles govern absorption, distribution and elimination MAC: Minimum Alveolar Concentration Potency measure 1 MAC is the concentration necessary to prevent responding in 50% of population [Halothane] % atm 0.0 0.5 1.0 1.5 Partial pressure - proportional to the concentration of anesthetic in gas or tissue at equilibrium Fraction of Anesthetized Patients 1.0 0.8 0.6 0.4 0.2 MAC 0.0 0.0 0.1 0.2 0.3 0.4 [Halothane] mm Factors decreasing MAC: Hypotension Anemia ( PCV < 13%). Hypothermia Metabolic acidosis Factors affecting MAC Extreme hypoxia (PaO2 < 38 mmhg ) Age: old animal require less anesthetic Premedication (opioids, sedatives, tranquilizers) Local anesthetics Pregnancy Hypothyroidism Concurrent use of nitrous oxide Factors increasing MAC: Increasing body temperature Hyperthyroidism Hypernatremia Factors NOT affecting MAC Type of stimulation Duration of anesthesia Species Sex PaCO2 between range of 14-95 mmhg Metabolic alkalosis PaO2 between range of 38-500 mmhg Hypertension Potassium Solubility & Pharmacokinetics Solubility expressed as partition coefficients (a ratio of the concentration of the agent in two phases at equilibrium) Blood:gas partition coefficient Solubility in blood main factor that determines the rate of induction and recovery Oil:gas partition coefficient fat solubility determines the potency of an anesthetic (as well as kinetics) Induction and Recovery The lower the blood:gas partition coefficient the faster the induction and recovery The lower the solubility in blood, the faster the process of equilibration Less drug has to be transferred via the lungs to the blood in order to achieve a given partial pressure A single lungful of air containing a low-solubility agent will bring the partial pressure in the blood closer to that of the inspired air Recovery is the same Low solubility in blood = fast induction and recovery High solubility in blood = slower induction and recovery Anesthetic Properties MAC Partition Coefficients Anesthetic (% atm) (mm) Water:Gas Oil:Gas Oil:Water Methoxyflurane 0.16 0.26 4.2 850 200 Halothane 0.77 0.19 0.63 200 320 Isoflurane 1.2 0.24 0.54 91 170 Enflurane 1.7 0.52 0.78 97 120 Diethylether 1.9 8.22 11 57 5.2 Sevoflurane 2.0 0.29 0.37 47 130 Fluroxene 3.4 0.95 0.71 67 94 Desflurane 6.0 0.52 0.22 19 86 Cyclopropane 9.2 0.72 0.20 9.7 49 Butane 20 0.15 0.019 15 790 Ethylene 67 2.2 0.085 1.1 13 Xenon 71 2.1 0.075 1.8 24 Nitrous Oxide 101 15 0.39 1.3 3.3 Potency Blood Solubility Brain Solubility 2

Nitrous Oxide Nitrous Oxide - Disadvantages Relatively safe Minimal effects on heart rate and blood pressure Little effect on respiration Low blood solubility (quick recovery) MAC value is 105% - Needs other agents for surgical anesthesia Weak anesthetic, powerful analgesic Cannot produce anesthesia without hypoxia Poor muscle relaxation Diffuses into closed spaces Inhibits vitamin B-12 metabolism Inhibits methionine synthetase (precursor to DNA synthesis) Abuse liability Anesthetics - Halogenated ethers Halothane (Fluothane ) 8 1 2 7 C C O C 6 5 4 MW 1 2 3 4 5 6 7 8 Diethyl ether 74 H H CH 3 H H H H H Fluroxene 126 H H =CH 2 H F F F Methoxyflurane 165 F H H H F Cl H Cl Desflurane 168 H F H F F F F F Isoflurane 184 H F H F Cl F F F Enflurane 184 F F H F F Cl H F Sevoflurane 200 H H F H CF 3 F F F 3 Most potent inhalational anesthetic MAC of 0.75% Very soluble in blood and adipose tissue Prolonged emergence Inhibits sympathetic response to painful stimuli Halothane - Disadvantages Enflurane ( Ethrane ) Decreases respiratory drive Depresses cardiovascular function Sensitizes myocardium -can lead to ventricular arrhythmias Halothane Hepatitis Malignant Hyperthermia Stable, nonflammable liquid with pungent odor MAC 1.68% Cardiac effects depression and decreased systemic vascular resistance inhibits sympathetic baroreflex response sensitizes myocardium Decreases respiratory drive Metabolism one-tenth that of halothane releases fluoride ion-- renal toxicity EpileptiformEEG patterns 3

Isoflurane (Forane ) Less soluble than halothane MAC of 1.30 % Excellent muscle relaxant Depresses respiratory drive and ventilatory responses-- (less than enthrane) Depresses cardiovascular system Myocardial depressant (less than enthrane) Isoflurane Toxic Side Effects Little metabolism (0.2%) -- low potential of organotoxic metabolites No EEG activity like enflurane Bronchoirritating, laryngospasm Inhibits sympathetic baroreflex response (less than enthrane) Produces most significant reduction in systemic vascular resistance Sensitizes myocardium - less than enthrane Sevoflurane (Ultane, Sevorane ) and Desflurane(Suprane ) Meyer Overton Correlation HAL Halothane 100 Low solubility in blood-- produces rapid induction and emergence Minimal systemic effects-- mild respiratory and cardiac suppression Few side effects Expensive ISO ENF SEV FLU DES CYC MOF DEE CHL DDM PFE CTF SHF CYC ETH NO2 XEN Isoflurane Enflurane Sevoflurane Fluroxene Desflurane Cyclopropane Methoxyflurane Diethylether Chloroform Dichlorodiflurormethane Perfluoroethane Carbon tetrafluroide Sulfur hexafluoride Cyclopropane Ethylene Nitrous oxide Xenon Mouse MAC (atm) 10 1 0.1 0.01 NIT CTF ARG PFE SHF KRY NO2 ETH XEN HYD DDM CYC FLU DEE ENF ISO HAL CHL MOF Potency k NIT Nitrogen 0.001 KRY ARG Krypton Argon 0.01 0.1 1 10 100 1000 Olive Oil : Gas Partition Coefficient Lipid- Based Theories of Anesthetic Action Hypothesized anesthetic effect was due to disruption of lipid bilayer of plasma membranes..however.. Volume expansion by nonanesthetic compounds Correlation between fluidity and anesthetic levels only occurred at high concentrations. Small changes in temperature did produce significant fluidity changes without causing anesthesia while large changes in anesthetic concentration produced small changes in fluidity. Cut-off effect - M- O rule only holds up to a certain size Inhalant anesthetics show stereoselectivity in effects 4

Protein-based theories of Anesthetic Action Ok, so which receptors matter. GABA A Glutamate (AMPA and NMDA) Anesthetics bind to hydrophobic/lipophilic sites on proteins. induce/prevent conformational change Glycine (strychnine-sensitive, in spinal cord and brainstem) Nicotinic ACh alter kinetics of conformational changes compete with ligands Injectable anesthetics Advantages minimal equipment direct CNS access wide variety of agents, techniques Disadvantages recovery dependent on uncontrollable factors individual variation in drug response potential for drug accumulation Barbiturates Phenobarbital Pentobarbital Sodium Thiopental Sodium Thiamylal Sodium Methohexital Barbiturates - General Very alkaline - very irritating to tissues Depress polysynaptic responses in the CNS Effect on GABA receptors Depress Reticular Activating System Depress sympathetic nervous system Poor analgesics Excitement at low doses Low therapeutic index! Cardiopulmonary Effects Arrhythmogenic!!! Transient VPCs & ventricular bigeminy Transient, moderate decrease in blood pressure Decrease cardiac contractility Vascular effects variable, but in general cause mild vasodilatation Respiratory depressants 5

Propofol GABA A positive modulator Solubilized in an emulsion Rapid onset, short duration of action, rapid smooth recoveries w/o hangover Useful for induction &/or maintenance (by constant infusion) Mild to moderate hypotension, may produce bradyarrhythmias Respiratory depressant, may produce apnea Disadvantages Expensive Moderate hypotension, possible bradyarrhythmias, respiratory depression (apnea not uncommon) Poor analgesia (need high doses) Drug vehicle supports bacterial growth Etomidate GABA A positive modulator non-barbiturate ultrashort sedative/hypnotic minimal cardiovascular effects rapid onset/recovery wide safety margin Dissociative Anesthetics Ketamine Tiletamine NMDA receptor channel blockers Produces amnesia, superficial analgesia, and catalepsy Dissociates the cortex from lower centers Both excitatory & depressant effects on EEG Actually has positive effects on CV measures and minimal respiratory depression Problems... Neuroleptanalgesia Seizures Muscle rigidity Poor visceral analgesia Increased secretions Poor recoveries - delirium Increased myocardial work load combination of opioid + tranquilizer/sedative produces state of light anesthesia useful for debilitated or geriatric patients eg fentanyl/diazepam; droperidol/fentanyl; oxymorphone/midazolam; etc... 6

Overview of mechanisms of action for general anesthetic.. Ion Channels and Anesthesia GABA A - primary anesthetic target Act as modulators, not direct agonists Increase current induced by low level GABA by >50% Work by prolonging channel open - time Inhalants, barbs, benzo s, steroids, propofol Glycine - important for spinal cord and lower brainstem GABA A Rc activation Ion Channels and Anesthesia Glutamate - NMDA, AMPA & Kainate Dissociative anesthetics Relatively insensitive to inhalants (?) and barbiturates nach - most simple anesthetics can stabilize desensitized form Definitely involved in many inhalant effects Increasing interest for role with other anesthetics Voltage gated ion channels - Na +, K +, Ca ++ Potential Receptor Targets Anesthetic GABA A Glycine Neuronal AMP A NMDA nach Halothane +++ +++ - - - - - - -/0 N 2O +++ +/0? -/0 - - - Xenon 0?? 0 - - - Barbiturates +++ +/0 - - - - - - 0 Ketamine 0 0 - - - 0 - - - Propofol +++ +++ -/0 -/0 -/0 Neuroste roids +++ 0 -/0 0 0 Do not appear to play a role in anesthesia 7