Difference between revisions of "Benzodiazepines"
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Benzodiazepines are primarily anxiolytics, but do have sedative effects in man and sick animals. They also cause muscle relaxation and are anticonvulsants. | Benzodiazepines are primarily anxiolytics, but do have sedative effects in man and sick animals. They also cause muscle relaxation and are anticonvulsants. | ||
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==Side Effects and Contraindications== | ==Side Effects and Contraindications== | ||
| − | Benzodiazepines give mild respiratory and cardiovascular suppression. They are however synergistic with central depressants such as barbiturates, antihistamines and alcohol. | + | Benzodiazepines give mild respiratory and cardiovascular suppression. They are however synergistic with central depressants such as barbiturates, antihistamines and alcohol. When administered to healthy animals, they can often act to increase levels of excitement, due to a disinhibition phenomenon. |
==Drugs in this Group== | ==Drugs in this Group== | ||
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Diazepam may be given orally or intravenously. Intravenous administration gives a rapid onset of action. The drug is dissolved in propylene glycol, which may cause thrombophlebitis, pain on injection and cardiac arrhythmias. | Diazepam may be given orally or intravenously. Intravenous administration gives a rapid onset of action. The drug is dissolved in propylene glycol, which may cause thrombophlebitis, pain on injection and cardiac arrhythmias. | ||
| − | As there are few cardiovascular side effect, diazepam is good for use as a premedicant. It can also be used with [[ | + | As there are few cardiovascular side effect, diazepam is good for use as a premedicant. It can also be used with [[Dissociative Agents#Ketamine|ketamine]] to induce and maintain anaethesia in the horse and in compromised small animals. |
===Midazolam=== | ===Midazolam=== | ||
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Inverse agonists act at the GABA receptor to close Cl<sup>-</sup> channels. They promote convulsions. | Inverse agonists act at the GABA receptor to close Cl<sup>-</sup> channels. They promote convulsions. | ||
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| + | [[Category:Sedatives and Tranquilisers]] | ||
| + | [[Category:Injectable Anaesthetic Agents]] | ||
Latest revision as of 16:38, 25 January 2011
Benzodiazepines are primarily anxiolytics, but do have sedative effects in man and sick animals. They also cause muscle relaxation and are anticonvulsants.
Mechanism of Action
GABA is an inhibitory neurotransmitter that opens post-synaptic Cl- channel to hyperpolarise the membrane and reduce the chance of action potential conduction occuring. Benzodiazepines modulate the GABA/Cl- channel complexes to enhance the effects of GABA. Benzodiazepines therefore have no intrinsic activity.
Side Effects and Contraindications
Benzodiazepines give mild respiratory and cardiovascular suppression. They are however synergistic with central depressants such as barbiturates, antihistamines and alcohol. When administered to healthy animals, they can often act to increase levels of excitement, due to a disinhibition phenomenon.
Drugs in this Group
Diazepam
Diazepam (Valium) gives a variable degree of sedation. It is a muscle relaxant and therefore should not be used as a sedative in horses. It is also an anticonvulsant, and is used to control status epilepticus. Diazepam also stimulates appetite.
Diazepam may be given orally or intravenously. Intravenous administration gives a rapid onset of action. The drug is dissolved in propylene glycol, which may cause thrombophlebitis, pain on injection and cardiac arrhythmias.
As there are few cardiovascular side effect, diazepam is good for use as a premedicant. It can also be used with ketamine to induce and maintain anaethesia in the horse and in compromised small animals.
Midazolam
Midazolam is similar to diazepam. It can be give i/m, i/v or orally, and is rapidly metabolised.
Benzodiazepine Antagonists
Benzodiazepine antagonists have no intrinsic efficacy, but prevent agonist interaction with receptors. Examples include flumazenil, which is used in man following benzodiazepine overdose.
Inverse Agonists
Inverse agonists act at the GABA receptor to close Cl- channels. They promote convulsions.