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Cholinergic mechanisms in physical dependence on barbiturates, ethanol and benzodiazepines

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TLDR
Accumulating data support the role of the cholinergic system in expressing symptoms of physical dependence on barbiturates, ethanol and benzodiazepines as well as in the permanent long-term effects observed after end of treatment.
Abstract
The aim of this review is to summarize the effects of acute and chronic treatment with barbiturates, ethanol and benzodiazepines on cholinergic mechanisms in the brains of experimental animals. A single dose of each of these substances reduces the turnover of ACh in the brain. Long-term treatment has the opposite effect; complicated interactions including decreased content of ACh are induced. Barbiturates have been shown to bind stereospecifically to muscarinic and nicotinic receptors in the brain, but this has not been observed for ethanol or the benzodiazepines. The effects on the cholinergic system are affected by the length of treatment and choice of treatment regimen. No effect on cholinergic parameters, such as muscarinic receptors, in the brain is observed on withdrawal of ethanol or barbiturate treatment when the animals are still tolerant towards the substances. The increase in the number of muscarinic receptors observed in several brain regions on withdrawal is seen as a sign of cholinergic supersensitivity. The number of receptors returns to normal when abstinence convulsions have occurred. The assumption of a cholinergic influence is supported by the finding that atropine, given as a single dose on the day of withdrawal of barbital, can prevent the muscarinic receptor changes. Furthermore, long-term barbital or ethanol treatment can induce permanent persistent changes in the cholinergic system in the brain. Cognitive defects and a significant permanent reduction in the content of ACh can be measured in rats which have had long-term barbital treatment. Similarly, a reduced number of muscarinic receptors has been measured in different brain regions of chronic alcoholics. Accumulating data support the role of the cholinergic system in expressing symptoms of physical dependence on barbiturates, ethanol and benzodiazepines as well as in the permanent long-term effects observed after end of treatment.

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Cognitive functions of cortical acetylcholine: toward a unifying hypothesis

TL;DR: While the proposed hypothesis implies that changes in activity in cortical ACh simultaneously occur throughout the cortex, the selectivity and precision of the functions of cholinergic function is due to its coordinated interactions with the activity of converging sensory or associational inputs.
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Cholinergic deficiency hypothesis in delirium: a synthesis of current evidence.

TL;DR: Current understanding of the cholinergic deficiency hypothesis in delirium is examined by synthesizing evidence on potential pathophysiological pathways, which may yield innovative approaches in the diagnosis, prevention, and treatment of this common, costly, and morbid condition.
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Nerve growth factor as a signaling molecule for nerve cells and also for the neuroendocrine-immune systems.

TL;DR: This review focuses on cellular events and presents a working model which attempts to explain the close interrelationships of the neuro-endocrine-immune triad via a modulatory action of NGF.
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Drugs of anesthesia acting on central cholinergic system may cause post-operative cognitive dysfunction and delirium

TL;DR: It seems possible to hypothesize that the inhibition of muscarinic cholinergic receptors could have a pivotal role in the pathogenesis not only of post-operative delirium but also the more complex phenomena ofPost-operative cognitive dysfunction.
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Cognitive functions of cortical ACh: lessons from studies on trans-synaptic modulation of activated efflux

TL;DR: Trans-synaptic modulation of cortical ACh efflux is a useful approach for determining the functions of cortex ACh and may offer some potential for the treatment of cognitive dysfunctions associated with impaired cortical cholinergic transmission.
References
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Journal ArticleDOI

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TL;DR: The molecular and cellular actions of three classes of abused drugs--opiates, psychostimulants, and ethanol--are reviewed in the context of behavioral studies of drug dependence.
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Ethanol inhibits NMDA-activated ion current in hippocampal neurons

TL;DR: The potency for inhibition of the NMDA-activated current by several alcohols is linearly related to their intoxicating potency, suggesting that alcohol-induced inhibition of responses to NMDA receptor activation may contribute to the neural and cognitive impairments associated with intoxication.
Journal ArticleDOI

Human Memory and the Cholinergic System: A Relationship to Aging?

David A. Drachman, +1 more
- 01 Feb 1974 - 
TL;DR: Comparisons of the memory and cognitive deficits induced by scopolamine with the performance of aged subjects revealed a marked similarity of pattern, and the possible theoretical explanations for the behavioral similarity seen with central cholinergic blockade and normal aging are discussed.
Journal ArticleDOI

N‐Methyl‐D‐Aspartate Receptors and Ethanol: Inhibition of Calcium Flux and Cyclic GMP Production

TL;DR: Measurements of calcium uptake and cyclic GMP production by cerebellar granule cells grown in primary culture demonstrated that ethanol preferentially inhibited N‐methyl‐D‐aspartate (NMDA) receptor‐gated cation channel function.
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