Sunday 8 July 2012

Methadone


Methadone Brand Names
Dolophine (US), Methadone Diskets, Methadone Intensol, Methadose, Metadol (Canadian)
Methadone is the Generic Name
Methadone Hydrochloride is belonged to analgesic and opioid pharmacologic category.

Indication / Use
Methadone is used to manage moderate-to-severe pain. Besides, it is also commonly used for detoxification and maintenance treatment of opioid addiction. However, it must be part of an FDA-approved program if it is intended to be used for the latter purpose.

Restrictions
When methadone is purposed for treatment of opioid addiction, it may only be dispensed in accordance to guidelines established by the Substance Abuse and Mental Health Services Administrations's (SAMHSA) Center for substance Abuse Treatment (CSAT).
However, regulations regarding methadone use may vary by state or different country. Advice should be obtained from appropriate regulatory agencies or consult with pain management care specialists before dispensing methadone.

There are regulatory exceptions to the General Requirement to Provide Opioid Agonist Treatment in which:
1. During inpatient care, when the patient was admitted for any condition other than concurrent opioid addiction, with the purpose to facilitate the treatment of the primary admitting diagnosis.
2. During an emergency period of no longer than 3 days while definitive care for the addiction is being sought in an  appropriately licensed facility

Pregnancy Risk Factor Category: C/D (dangerous especially in prolonged used or at high doses)
Some animal studies have shown teratogenic effects, however, the data collected by Teratogen Information System are complicated by other factors including maternal use of illicit drugs, nutrition supplement, concurrent infections and psychosocial circumstances.
Though, there is improvement being observed in pregnant women with methadone treatment compared to pregnant women using illicit drugs.

Methadone can be detected in the amniotic fluid, cord plasma, and newborn urine. Fetal growth, birth weight, length, head or other s may be affected and decreased in infants born to narcotic-addicted mothers with methadone treatment during pregnancy. Growth deficits do not appear to persist but decreased performance on psychometric and behavioural tests has been found to continue into childhood.

Besides, there is also report of abnormal fetal nonstress tests where withdrawal symptoms in the neonate may be observed up to 2-4 weeks after delivery.
Hence, methadone should be only used during pregnancy when clearly needed where benefits outweigh risk.

Since methadone clearance is increased and half-life is decreased during 2nd and 3rd trimesters of pregnancy, withdrawal symptoms may be observed in the mother and thus, methadone dosage may need to be increased and adjusted or decreasing dosing interval during pregnancy.
Methadone may enter into breast milk and is not recommended to be used during lactation.

Safety issues
Methadone is always confused with sound or look alike drugs such as dexmethylphenidate or methylphenidate.
Methadone has been listed in the drug classes under the Institute for Safe Medication Practices (ISMP) which may post heightened risk or harm to patient when used in error.

Contraindications
Respiratory depression in which in the absence of resuscitative equipment or in an unmonitored condition, acute bronchial asthma or hypercarbia, paralytic ileus, concurrent use of selegiline

Precautions
As with other opioid-containing analgesic regimen, methadone should be tailored to each patient's needs and based on the type of pain being managed, such as the factors of acute versus chronic, route of administration, degree of tolerance for opioids, age, weight, and other medical conditions. Also, the optimal analgesic dose varies widely among different individuals and methadone doses should be titrated to pain relief. Patients on stable maintenance doses of methadone may require higher doses in case of acute pain, for example during postoperative pain and physical trauma. It is noted that methadone is ineffective for anxiety relief.

Methadone may prolong the QT interval and increase risk of torsade de pointes. Before starting methadone treatment, patients should be informed of the potential arrhythmia risk, and assessed for history of structural heart disease, arrhythmia, syncope, or any potential drug interactions including drugs that prolong QT interval, induce hypokalemia, hypomagnesemia, or hypocalcemia, or reduce methadone clearance. ECG baseline should be obtained for all patients and evaluate the risk according to QT interval monitoring.


Methadone must be used iwth caution in patients at risk for QT prolongation, taking medications that would prolong the QT interval, electrolyte depletion inducer or history of conduction abnormalities. Normally QT interval prolongation and torsade de pointes is associated with high doses or greater 100 mg/day, however, it has also been observed with lower doses used.

Methadone may also cause severe hypotension and should be used cautiously  in case of severe volume depletion or abnormal blood pressure, cardiovascular disease or dysrhythmias.
Methadone may also cause respiratory depression and care must be taken when used in patinets with respiratory disease or pre-existing respiratory conditions such as severe obesity, asthma, COPD, sleep apnea, or CNS depression. Since the respiratory effects last longer than the analgesic effects, slow titration of methadone doses is required. Attention and care should be emphasized when initiating methadone treatment on dose titration and conversion from other opioid agonists. Incomplete cross tolerance may occur patient may not be tolerant to methadone even though tolerant to other mu opioid agonists. Abrupt cessation must be avoided as may precipitate withdrawal symptoms.

Methadone may cause CNS depression which impair physical or mental abilities and thus should be cautioned in performing tasks requiring mental alertness such as operating machinery or driving after taking methadone. Sedative drugs or ethanol may potentiate methadone effects. Use with caution in patients with depression or suicidal tendencies or history or drug abuse. Psychological and physical dependence may occur with prolonged use.


Also, patient with head injury or increased intracranial pressure must be taken extra care. Patients with acute abdominal conditions may obscure diagnosis or clinical course.. Elderly patients is more susceptible to methadone side effects such as CNS, respiratory and gastrointestinal effects and hence, lower initial dose should be used in elderly or debilitated,  or in patients with abnormal thyroid metabolism, obesity, adrenal insufficiency, prostatic hyperplasia or urethral stricture and also in impaired renal and hepatic function.
It must be noted that safety and efficacy of methadone use has not been established in children.

Methadone Adverse Reactions
Adverse effects of methadone may decrease over several weeks with prolonged administration. However, constipation and sweating may persist.


Cardiovascular: arrhythmia, bigeminal rhythms, radycardia, cardiac arrest, cardiomyopathy, 


ECG changes, edema, extrasystoles, faintness, flushing, heart failure, hypotension, palpitation, peripheral vasodilation, phlebitis, orthostatic hypotension, QT interval prolonged, shock, syncope, tachycardia, torsade de pointes, T-wave inversion, ventricular fibrillation, ventricular tachycardia


Central nervous system: Agitation, confusion, disorientation, dizziness, drowsiness, dysphoria, euphoria, hallucination, headache, insomnia, light-headedness, sedation, seizure


Dermatologic: Hemorhagic urticaria, pruritus, rash, urticaria (more common when administered intravenously but are rare side effects)


Endocrine & metabolic: Antidiuretic effect, amenorrhea, hypokalemia, hypomagnesemia, decreased libido


Gastrointestinal: Abdominal pain, anorexia, biliary tract spasm, constipation, glossitis, nausea, stomach cramps, vomiting, weight gain, xerostomia


Hematologic: Thrombocytopenia which is reversible, reported in patients with chronic hepatitis


Neuromuscular & skeletal: weakness


Local (intramuscular or subcutaneous injection): Erythema, pain or swelling.


Ocular Miosis, visual disturbances


Respiratory: Pulmonary edema, respiratory depression, respiratory arrest


Miscellaneous: Death, diaphoresis, physical and psychological dependence

Reference:
Charles F. Lacy, Lora L. Armstrong, Morton P. Goldman, Leonard L.Lance. Drug Information Handbook 18th Edition. 2009-2010.
Lexi-Comp is the official drug reference for the American Pharmacists Association.

Sunday 17 June 2012

Buspirone HCl Reviews | Advantages, Mechanism of action, Side effects


Buspirone
Buspirone is non-benzodiazepine anxiolytic which is the most selective anxiolytic currently
Mechanism of Action
-anxiety associated with altered serotonin transporters
-partial agonist at 5-HT 1A receptor presynaptic
-inhibit serotoin release
-dose not involve GABA receptors
-delayed onset (~ 1-2 week)
-pregnancy category: B
-oral administration

Advantages
-lack CNS depressant effect
-no sedation
-no impairment of performance
-no tolerance or withdrawal
-no cross-tolerance with BDZ
-no abuse/addiction potential
-minimal effect on psychomotor functions

Binding of a partial agonist to the 5-HT1A receptor causes the dissociation of inhibitory G-proteins. The G-protein alpha sub-unit binds to and inhibits adenylate cyclase. This prevents the conversion of ATP to cAMP and the initiation of other secondary messenger signaling mechanisms, hence cell depolarisation is inhibited.

Pharmacokinetics
-rapidly absorbed and undergo extensive first pass metabolism
-oxidised by CYP3A4 to active metabolite
-excretion through urine (30-60%) and feces (20-40%)
-t1/2 2-11 hours

Side effects
-dizziness, drowsiness, headache, nervousness
-tachycardia/ palpitations
-parethesia
-GI distress, N/D
-pupillary constrition (dose-dependent)

Drug-drug interactions
+fluoxetine = reduce buspirone effect
+haloperidol = increase p [haloperidol]
+CYP3A4 inducer (carbamazepine, barbiturates, phenyton) = reduce p [buspirone]
+CYP3A4 inhibitor (erythromycin, azole, protease, inh) = increase p [buspirone]
+MAOIs = risk of elevated BP


Related Searches:
Buspirone HCl Advantages, Mechanism of action
Clonazepam Side effects, Drug interactions
Lorazepam Side effects, Drug Interactions
Diazepam Side effects,Drug interactions
Alprazolam Side effects, Drug interactions
Benzodiazepines Drug-Drug Interaction
Benzodiazepine pregnancy category | Teratogenicity
Benzodiazepine Withdrawal Symptoms | high dose or low dose
Benzodiazepines Overdose & Management | Flumnezil
Benzodiazepines drowsiness, sedation, euphoria, amnesia
Benzodiazepines Advantages & Disadvantages
Benzodiazepines List of Examples Drugs | Mechanism of action
Barbiturates Drugs List | Side effects, Mechanism of action
GABA Receptors Wiki | Function, Classification, Location
Anxiolytics List of Examples Drugs - Benzodiazepines
Obsessive-Compulsive Disorder | cleaning, checking, repeating
Anxiety Pathophysiology | Causes
Anxiety Classification | Manifestations - characteristic
Anxiolytics Drugs Definition | Dependence, Side effects
Anxiety Disorders | Definition, Symptoms, Treatment

Clonazepam Side effects, Drug interactions, pharmacokinetics


Clonazepam
Pharmacokinetics          - oral administration
                        - rapidly absorbed with bioavailability ~ 90%
                        - highly metabolised in liver
                        - excretion in urine (<2% unchanged drug) and into breast milk
                        - t1/2 2-11 hours

Side effects
CNS: somnolence, dizziness, disorientation, depression, memory disturbance, decreased libido
CVS: hypotension
GI: constipation, decrease appetite
Others: dysmenorrhoea

Drug-drug interactions
+ cimetidine, disulfiram, OC = increase clonazepam effect
+ CYP inducer (carbamazepine, barbiturates, phenytoin) = reduce p [clonazepam]
+ digoxin = increase p [digoxin]
+ theophylline = antagonize sedative effect

Lorazepam Side effects, Drug Interactions, Administration


Lorazepam
Administration: oral, IM, IV (slow)
Pharmacokinetics          - absolute bioavailability ~ 90%
                        - rapidly conjugated to lorazepam glucuronide
                        - t1/2 1-2 hour (lorazepam)
                        - t1/2 ~ 18 hours (lorazepam glucuronide)
Side effects
CNS: confusion, dizziness, fatigue, memory impairment, disorientation, headache
CVS: hypotension
GI: N/V/D/C, dry mouth, dysphagia

Drug-drug interactions
+ Oral contraceptive = increase clearance rate of lorazepam
+ theophylline = antagonize sedative effect
+ scopolamine = increase incidence of hallucinations, irrational behaviour & sedation

Diazepam Side effects,Drug interactions, Pharmacokinetics


Diazepam (Valium)
Administration: oral, rectal, IM, IV (slow)
Pharmacokinetics          - complete oral bioavailability
                        - highly lipophilic
                        - crosses placenta & excreted in breast milk
                        - metabolised to desmethyldiazepam (active)
Side effects
CNS: confusion, dizziness, fatigue, memory impairment, disorientation, headache
CVS: hypotension, tachycardia
GI: N/V/D/C, dry mouth
others: rash, dependency/withdrawal symptoms
Contraindications: psychoses, lactation

Drug-drug interactions
+ cimetidine, disulfiram, OC = increse effect of diazepam
+ theophylline = antagonize sedative effect
+ omeprazole = increase p [diazepam]

Alprazolam Side effects, Drug interactions, Pharmacokinetics


Alprazolam (Xanax)
Pharmacokinetics        - oral administration with rapid absorbed and almost complete oral bioavailability
                        - crosses placenta & excreted in breast milk
                        - metabolisd to alfa-OH alprazolam (active) & benzophenone der. (inactive)
                        - excreted in urine (~20% unchanged)

Side effects
CNS: drowsiness, fatigue, sedation, memory impairment, cognitive disorder, somnolence, lightheadness, decreased libido, depression, confusion
CVS: hypotension, tachycardia
GI: N/V/D/C, dry mouth
Others: menstrual disorder, rash
Contraindications: patients receiving itra/ketoconazole

Drug-drug interactions
+ cimetidine, disulfiram, oral contraceptive = increase effect of alprazolam
+ theophylline = antagonize sedative effect
+ omeprazole = increase p [alprazolam]
+ imipramine, desipramine = increase p [imi/desipramine]

Benzodiazepines Drug-Drug Interaction


Benzodiazepines Drug-Drug Interaction
+ CNS depressants/alcohol > additive > increase CNS depression
+ CYP3A4 inhibitor > increase plasma [benzodiazepiens]
examples include:
azole antifungal agents (itraconazole, ketoconazole)
diltiazem
SSRIs (fluoxetine, fluvoxamine)
grapefruit juice
isoniazid
erythromycin
nefazodone
non-nucleoside reverse transcriptase inhibitors (delavirdine, efavirenz)
protease inhribitors (indinavir)
+ CYP3A4 inducer > decrease plasma [benzodiazepines]
examples include carbamazepine and rifampin
+ flumazenil = antagonism
*Combination of anxiolytic drugs should be avoided



Related Searches:
Buspirone HCl Advantages, Mechanism of action
Clonazepam Side effects, Drug interactions
Lorazepam Side effects, Drug Interactions
Diazepam Side effects,Drug interactions
Alprazolam Side effects, Drug interactions
Benzodiazepines Drug-Drug Interaction
Benzodiazepine pregnancy category | Teratogenicity
Benzodiazepine Withdrawal Symptoms | high dose or low dose
Benzodiazepines Overdose & Management | Flumnezil
Benzodiazepines drowsiness, sedation, euphoria, amnesia
Benzodiazepines Advantages & Disadvantages
Benzodiazepines List of Examples Drugs | Mechanism of action
Barbiturates Drugs List | Side effects, Mechanism of action
GABA Receptors Wiki | Function, Classification, Location
Anxiolytics List of Examples Drugs - Benzodiazepines
Obsessive-Compulsive Disorder | cleaning, checking, repeating
Anxiety Pathophysiology | Causes
Anxiety Classification | Manifestations - characteristic
Anxiolytics Drugs Definition | Dependence, Side effects
Anxiety Disorders | Definition, Symptoms, Treatment

Benzodiazepine pregnancy category | Teratogenicity


Benzodiazepine: Teratogenicity
Pregnancy category: D
Studies in pregnant women have demonstrated a risk to the foetus. However, the benefits of therapy in a life threatening situation or a serious disease, may outweight the potential risk
Newborn infants show withdrawal if mother used benzodiazepines
Benzodiazepines during labor can have effects on newborn
            -depressed respiration and feeding
            -floppy baby syndrome
            -low apgar scores

Related Searches:
Buspirone HCl Advantages, Mechanism of action
Clonazepam Side effects, Drug interactions
Lorazepam Side effects, Drug Interactions
Diazepam Side effects,Drug interactions
Alprazolam Side effects, Drug interactions
Benzodiazepines Drug-Drug Interaction
Benzodiazepine pregnancy category | Teratogenicity
Benzodiazepine Withdrawal Symptoms | high dose or low dose
Benzodiazepines Overdose & Management | Flumnezil
Benzodiazepines drowsiness, sedation, euphoria, amnesia
Benzodiazepines Advantages & Disadvantages
Benzodiazepines List of Examples Drugs | Mechanism of action
Barbiturates Drugs List | Side effects, Mechanism of action
GABA Receptors Wiki | Function, Classification, Location
Anxiolytics List of Examples Drugs - Benzodiazepines
Obsessive-Compulsive Disorder | cleaning, checking, repeating
Anxiety Pathophysiology | Causes
Anxiety Classification | Manifestations - characteristic
Anxiolytics Drugs Definition | Dependence, Side effects
Anxiety Disorders | Definition, Symptoms, Treatment

Benzodiazepine Withdrawal Symptoms | high dose or low dose withdrawal


Benzodiazepine Withdrawal Syndrome
High dose withrawal
-similar symptoms with alcohol withdrawal
-seizures
-delirium
-tremors
-cramps
-depression
-insomnia
-higher than therapeutic dose for more than a month

Low dose withdrawal
-symptoms different from alcohol withdrawal
-irregular heart beat
-anxiety
-weight loss
-muscle spasms
-impairment of memory & concentration
-increase blood pressure
-sensitive to light/sounds
-tinglign feeling
-feelings of unreality
-numbness
-therapeutic dose longer than 3 months
-should not be confused with symptom remergence


Related Searches:
Buspirone HCl Advantages, Mechanism of action
Clonazepam Side effects, Drug interactions
Lorazepam Side effects, Drug Interactions
Diazepam Side effects,Drug interactions
Alprazolam Side effects, Drug interactions
Benzodiazepines Drug-Drug Interaction
Benzodiazepine pregnancy category | Teratogenicity
Benzodiazepine Withdrawal Symptoms | high dose or low dose
Benzodiazepines Overdose & Management | Flumnezil
Benzodiazepines drowsiness, sedation, euphoria, amnesia
Benzodiazepines Advantages & Disadvantages
Benzodiazepines List of Examples Drugs | Mechanism of action
Barbiturates Drugs List | Side effects, Mechanism of action
GABA Receptors Wiki | Function, Classification, Location
Anxiolytics List of Examples Drugs - Benzodiazepines
Obsessive-Compulsive Disorder | cleaning, checking, repeating
Anxiety Pathophysiology | Causes
Anxiety Classification | Manifestations - characteristic
Anxiolytics Drugs Definition | Dependence, Side effects
Anxiety Disorders | Definition, Symptoms, Treatment

Benzodiazepines Overdose & Management | Flumnezil


Benzodiazepines Overdose & Management
Benzodiazepines is relatively safe in overdose
Acute Overdose causes -prolonged sleep
                                    -no serious respiratory depression
                                    -no coma
Fatal Overdose - incidence is low and more likely to occur when used in combination with other CNS depressants eg. alcohol, barbiturates
Management     -flumazenil which is benzodiazepines antagonist
                        -respiratory function adequately supported and monitored

Related Searches:
Buspirone HCl Advantages, Mechanism of action
Clonazepam Side effects, Drug interactions
Lorazepam Side effects, Drug Interactions
Diazepam Side effects,Drug interactions
Alprazolam Side effects, Drug interactions
Benzodiazepines Drug-Drug Interaction
Benzodiazepine pregnancy category | Teratogenicity
Benzodiazepine Withdrawal Symptoms | high dose or low dose
Benzodiazepines Overdose & Management | Flumnezil
Benzodiazepines drowsiness, sedation, euphoria, amnesia
Benzodiazepines Advantages & Disadvantages
Benzodiazepines List of Examples Drugs | Mechanism of action
Barbiturates Drugs List | Side effects, Mechanism of action
GABA Receptors Wiki | Function, Classification, Location
Anxiolytics List of Examples Drugs - Benzodiazepines
Obsessive-Compulsive Disorder | cleaning, checking, repeating
Anxiety Pathophysiology | Causes
Anxiety Classification | Manifestations - characteristic
Anxiolytics Drugs Definition | Dependence, Side effects
Anxiety Disorders | Definition, Symptoms, Treatment

Benzodiazepines drowsiness, sedation, euphoria, amnesia | Benzodiazepines Side effects


Side effects of Benzodiazepines
Central nervous system - headache, drowsiness, excess sedation, impaired coordination, confusion, anterograde amnesia, euphoria, fatigue
Paradoxical reactions - increased anxiety, insomnia, hyperexcitability, hallucination
Gastrointestinal disturbance - nause, vomiting, diarrhea, constipation, dry mouth
Others  - BDZs have wide margin of safely if used for short periods
            - prolonged use (beyond several weeks) may cause Physical Dependence and Psychologic Dependence
            - withdrawal syndrome can occur with BDZs
            - tolerance may develop to CNS ADR and anxiolytic effect upon chronic use

Related Searches:
Buspirone HCl Advantages, Mechanism of action
Clonazepam Side effects, Drug interactions
Lorazepam Side effects, Drug Interactions
Diazepam Side effects,Drug interactions
Alprazolam Side effects, Drug interactions
Benzodiazepines Drug-Drug Interaction
Benzodiazepine pregnancy category | Teratogenicity
Benzodiazepine Withdrawal Symptoms | high dose or low dose
Benzodiazepines Overdose & Management | Flumnezil
Benzodiazepines drowsiness, sedation, euphoria, amnesia
Benzodiazepines Advantages & Disadvantages
Benzodiazepines List of Examples Drugs | Mechanism of action
Barbiturates Drugs List | Side effects, Mechanism of action
GABA Receptors Wiki | Function, Classification, Location
Anxiolytics List of Examples Drugs - Benzodiazepines
Obsessive-Compulsive Disorder | cleaning, checking, repeating
Anxiety Pathophysiology | Causes
Anxiety Classification | Manifestations - characteristic
Anxiolytics Drugs Definition | Dependence, Side effects
Anxiety Disorders | Definition, Symptoms, Treatment

Benzodiazepines Advantages & Disadvantages | Pharmacokinetics


Benzodiazepines
Advantages
-higher therapeutic index
-relatively safe even if overdose
-have little effect on respiratory depression
-muscle relaxation (useful for spasm & back pain)
-can treat seizures (clonazepam)

Disadvantages
-interaction with alcohol
-long-lasting 'hangover' effects
-withdrawal symptoms
-development of TOLERANCE

Pharmacokinetics of Benzodiazepines
Pharmacokinetic properties determine the choice of drug for different clinical conditions
Absorption       - BDZs are weak bases, mainly absorbed from duodenum
                        - given orally - well & rapidly absorbed
Distribution      - most BDZs extensively protein bound (85%-95%)
                        - large volume of distribution VD - accumulation in body fat (high lipid solubility)
                        - increase lipid solubility > high rate of entry into CNS > faster onset
                        - all BDZ cross placenta
                        - detectable in breast milk > may exert depression effects on the CNS of lactating infants
Metabolism      - Metabolism: BDZs undergo extensive metabolism - Oxidation either by N-dealkylation or hydroxylation
                        - mostly by CYP3A4 or CYP2C19
                        - conjugation (glucuronides)
                        - conversion to active/inactive metabolite is an important distinction
                        - some BDZs are prodrugs & require metabolism (clorazepate)
                        - many have active metabolites with t1/2 greater than parent drug (long duration of action)
Excretion         - mostly via urine
                        - as metabolites (predominantly glucuronides)


Related Searches:
Buspirone HCl Advantages, Mechanism of action
Clonazepam Pharmacokinetics
Lorazepam Pharmacokinetics
DiazepamPharmacokinetics
Alprazolam Pharmacokinetics
Benzodiazepines Drug-Drug Interaction
Benzodiazepine pregnancy category | Teratogenicity
Benzodiazepine Withdrawal Symptoms | high dose or low dose
Benzodiazepines Overdose & Management | Flumnezil
Benzodiazepines drowsiness, sedation, euphoria, amnesia
Benzodiazepines Advantages & Disadvantages
Benzodiazepines List of Examples Drugs | Mechanism of action
Barbiturates Drugs List | Side effects, Mechanism of action
GABA Receptors Wiki | Function, Classification, Location
Anxiolytics List of Examples Drugs - Benzodiazepines
Obsessive-Compulsive Disorder | cleaning, checking, repeating
Anxiety Pathophysiology | Causes
Anxiety Classification | Manifestations - characteristic
Anxiolytics Drugs Definition | Dependence, Side effects
Anxiety Disorders | Definition, Symptoms, Treatment

Benzodiazepines List of Examples Drugs | Mechanism of Action, Therapeutic uses


Benzodiazepines
Chlordiazepoxide (Benpine, oldest)
Diazepam (Valium)
Bromazepam (Lexotan)
Lorazepam (Ativan)
Chlorazepate (Tranxene)
Alprazolam (Xanax)
Clonazepam
Oxazepam
Prazepam

Benzodiazepines Mechanism of Action
Involvement of endogenous ligands of the BDZ receptors is suspected.
BDZ bind selectively to GABA A receptors, in which binding of BDZs to gamma subunits of GABA A facilitates the process of channel opening
BDZs enhance the GABAnergic transmission by
-increase the frequency of openings of GABAergic channels
-increase receptor affinity for GABA
Serotonergic effects may result, eg. clonazepam

Benzodiazepines bind to GABA A receptors (gamma subunit) > act allosterically to increase the affinity of GABA > facilitate the opening of the Cl- ion channel - increased chloride permeability. Hence, BDZ potentiate GABA by increasing neuronal inhibition and CNS depression especially limbic system.

Benzodiazepiens therapeutic uses
Reduction of anxiety and agression
Sedation and induction of sleep
-anxiolysis (20% receptor occupancy with alfa2)
-sedation (30-50% receptor occupancy with alfa1)
-hypnosis (>60% receptor occupancy)
In addition, BDZ are used in/as:
-alcohol withdrawal
-pre-anesthetic medications
-reduction of muscle tone and coordination
-anticonvulsant
-anterograde amnesia

Related Searches:
Buspirone HCl Advantages, Mechanism of action
Clonazepam Pharmacokinetics
Lorazepam Pharmacokinetics
DiazepamPharmacokinetics
Alprazolam Pharmacokinetics
Benzodiazepines Drug-Drug Interaction
Benzodiazepine pregnancy category | Teratogenicity
Benzodiazepine Withdrawal Symptoms | high dose or low dose
Benzodiazepines Overdose & Management | Flumnezil
Benzodiazepines drowsiness, sedation, euphoria, amnesia
Benzodiazepines Advantages & Disadvantages
Benzodiazepines List of Examples Drugs | Mechanism of action
Barbiturates Drugs List | Side effects, Mechanism of action
GABA Receptors Wiki | Function, Classification, Location
Anxiolytics List of Examples Drugs - Benzodiazepines
Obsessive-Compulsive Disorder | cleaning, checking, repeating
Anxiety Pathophysiology | Causes
Anxiety Classification | Manifestations - characteristic
Anxiolytics Drugs Definition | Dependence, Side effects
Anxiety Disorders | Definition, Symptoms, Treatment

Barbiturates Drugs List | Side effects, Mechanism of Action, Dependence


Barbiturates
Now largely obsolete as anxiolytic and are mainly used in anesthesia (thiopental) and epilepsy (phenobarbital)
Taking BARBs with other CNS depressants can be extremely dangerous and may even lethal
Examples include: alcohol, tranquillizers, opioids (heroin, morphine, codeine or methadone), and antihistamines (found in cold, cough, and allergy remedies)

Barbiturate Mechanism of Action
Enhance  GABAnergic Transmission
-increase opening time of GABAnergic channels both in the presence or absence of GABA
-increase receptor affinity for GABA
However, they bind to a different site of the GABA A - receptor / chloride channel. At high concentrations they may be GABA-mimetic
Barbiturates are less selective than benzodiazepines, they also:
-depress actions of excitatory neurotransmitters
-exert nonsynaptic membrane effects

Disadvantages of Barbiturates
-increase toxicity compared to benzodiazepenes
-psychological dependence
-physiological tolerance: No tolerance to lethal action of drug
-strongly induce hepatic CYP450 & conjugating enzymes > increase metabolism of many other drugs
-flumazenil not effective
-death may occur by overdose (often choice to commit suicide)

In low doses, have a tranquilizing effect. As dose increases, hypnotic or sleep inducing effect. Even large doses actas anticonvulsants and anesthetics. Barbiturates has small therapeutic index.
Sedation > hypnosis > anesthesia > coma > death

Barbiturates Adverse effects
-excessive CNS depression
-hypersensitivity reactions
-excitement
-respiratory depression and hypotension
-coma and death in overdose

GABA Receptors Wiki | Function, Classification, Location, Repair, Anxiety


GABA receptors Classification
3 major subtypes of trans-membrane proteins
GABA A - 5 subunits, coassemble to form an integral, involves ionotropic chloride channel
GABA B - it is single, G protein-coupled, metabotropic receptor
GABA C - ligand-gated chloride channel, function and pharmaco properties are different from GABA A & B

GABA A Receptors
GABA A receptors is a glycoprotein pentamer belonged to of ligand-gated ion channelfamily
The GABA A receptor-chloride ionophore complex is made of 5 subunits, alfa, beta and gamma that co-assemble to form an integral chloride channel
There are 6 subtypes of alfa, and 3 each of beta and gamma
GABA binds to a site on the alfa or beta subunit
The receptor also contains binding sites for benzodiazepines, barbiturates and steroids such as progesterone (distinct from the GABA-binding site)

Functional Diversity of the GABA A Receptor Subunits
alfa1 subunit - containing GABA A receptors: sedation
alfa2 subunit - anxiolysis
alfa3 subunit - processing of sensory motor information related to a schizophrenia endophenotype
alfa4 subunit - sedative, hypnotic and anesthetic effects of some agents in the thalamus
alfa5 subunit - (extrasynaptic): associative temporal and spatial memory by inhibitory modulation of activities in the hippocampus
beta3 subunit - sedation, hypnosis, and anesthesia

GABA Function and Distribution
Inhibitory neurotransmitter that modulate chloride anion permeability
Widely distributed thoughout central nervous system
Local inhibitory action, therefore rapidly alters neuronal output
GABA is responsible for overall level of inhibitory tone in the brain

GABA binds to GABA A receptors --> causes conformational changes --> open the chloride ion channel --> lead to neuronal membraine hyperpolarization --> inhibitory neurotransmission in the CNS

Anxiolytics List of Examples Drugs - Benzodiazepines


Anxiolytics
An effective anxiolytic agent should reduce anxiety with little or no effect on motor and mental function
·         Benzodiazepines (BZDs)
·         Barbiturates (BARBs)
·         5-HT1A receptor agonists
·         Carbamates
·         Others:TCAs (fluvoxamine), MAOIs, Antihistaminicagents, B-Adrenoreceptor antagonists, Antipsychotics (Ziprasidone)

Overdose effects of an ideal antianxiety/sedative agent should not include generalized CNS depression. Therapeutic Index, margin of safety is greater for 2nd generation agents thatn for 1st generation agents. While increasing the dose, anxiolytics may give effects of sedation to hypnosis and anesthesia
First generation - eg. barbiturates
2nd generation - eg. benzodiazepines
3rd generation - Selective antianxiety, eg.buspirone

Obsessive-Compulsive Disorder | cleaning, checking, repeating


Obsessive-Compulsive Disorder
Obsessions - irrational, disturbing thoughts that intrude into consciousness
Compulsions - repetitive behaviour or rituals performed to alleviate obsessions
Performance of these rituals neutralize the anxiety, however relief is only temporary
- Cleaning: repeatedly washing hands or cleaning home
- Checking: check several or even hundreds of times to make sure that stoves are turned off or doors are locked
- Repeating: some repeat a name, phrase or action over and over