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Sedative hypnotic
Sedative hypnotic

... “Z Drugs” are a group of nonbenzodiazepine drugs with effects similar to benzodiazepines which are used in the treatment of insomnia and whose names mostly start with the letter “Z”. ...
Drug and Alcohol Use, Abuse and Prevention Information
Drug and Alcohol Use, Abuse and Prevention Information

... o Mescaline: derived from peyote cactus. Ceremonial drug of Native Americans. Generates an LSD effect with some amphetamine properties. Can last 12 hrs. o Psilocybin/Psilocin: psychoactive ingredient in Psilocybe mexicana (magic mushrooms). Acts on the brain for ~2-4 hours. o MDMA (ecstasy)—hallucin ...
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... CONCLUSIONS: Benzodiazepine exposure in the elderly increases the risk of hip fractures. This is true even with modest dosage, short-acting agents and short-term exposures. Clinicians should prescribe benzodiazepines judiciously with the elderly to minimize drug-related hip fractures. ...
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... Clozapine =atypical neuroleptic - improves performance of chronic PCP monkeys in object retrieval task -increases basal dopamine concentration in frontal cortex ...
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... et al, 2000). Although clozapine and quetiapine seem to be exceptions, this rule also applies for most of the secondgeneration, 'atypical' antipsychotics (Nyberg et al, 1999). When their doses are raised above a certain threshold, striatal (and potentially extrastriatal) D2 DA occupancy increases to ...
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Amphetamines, Ketamine and LSD

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AADC Gene Therapy for Parkinson`s Disease
AADC Gene Therapy for Parkinson`s Disease

... a gene, AADC (aromatic amino acid decarboxylase) into the brains of people with moderately advanced Parkinson’s disease. In this study, the AADC gene will be delivered to a specific area of the brain and it may increase dopamine production in the brain. It is the third study of its kind. The study w ...
Drugs acting on digestive system
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... cortex, and perhaps secondarily inhibits the hunger center. However, due to the fact that amphetamine refers to the active psychoactive drugs and has a pronounced peripheral sympathomimetic properties when applied arise anxiety, insomnia, tachycardia, increased blood pressure may develop physical dr ...
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... – Reserpine was known to be a dopamine antagonist (it depleted the brain of dopamine by causing them to leak from their vessicles) – Stimulants, which are agonists of dopamine trigger schizophrenic episodes in healthy subjects at high doses (cocaine psychosis and amphetamine psychosis) ...
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... Regardless of whether the medicine you are taking is a prescription or an over the counter drug, you should read all of the warnings and dosage information to ensure that you do not have any unwanted side effects. ...
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... (ALS). The mRNA targets of TDP-43 in the human brain and its role in RNA processing are largely unknown. Using individual nucleotide-resolution ultraviolet cross-linking and immunoprecipitation (iCLIP), we found that TDP-43 preferentially bound long clusters of UG-rich sequences in vivo. Analysis of ...
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... been proposed that the slow inactivation pathway is more prominent during prolonged depolarisation, as might be expected during epileptiform discharges. Calcium channels. Voltage-gated calcium channels represent another important target for several antiepileptic agents. The efficacy of ethosuximide ...
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... in ophthalmic commercial use; however, that may soon change. Two anti-integrin agents are in US clinical trials for ophthalmic use: lifitegrast (Shire), a compound with the potential to treat ocular surface inflammation that is nearing US Food and Drug Administration (FDA) approval, and ALG-1001 (Lu ...
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... 4. Drugs affecting Action: a. Inhibitors (antagonists) This is the main area of neuromuscular synaptic pharmacology. The binding of ACh to its receptors at NMJ epitomises the general equation: A+RARAR*, with the ‘starred’ state of the agonist-receptor (AR) complex corresponding to the open-pore st ...
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... Types of Tolerance Pharmacodynamic Tolerance  decreased NT synthesis  Down-regulation of receptors  Behavioral Tolerance  Volitional vs. Associative  Cross Tolerance  tolerance to 1 drug  also to a 2d  e.g., alcohol & phenobarbitol ~ ...
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... 2) Understand the major mechanisms through which genetic variation can alter responses to drugs. The most common type of variation change is a change in a single nucleotide pair termed a single nucleotide polymorphism or SNP. If SNPs occur in the coding region of a gene they can have qualitative eff ...
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Central Nervous Stimulants

... Respiratory Stimulants (Analeptics) • Used to antagonize respiratory depression caused by overdosage with CNS depressants; Doxapram • Act on respiratory center in the brain stem as well as on peripheral carotid chemoreceptors to increase the depth and rate of respiration • Doxapram: use/reversal of ...
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... • drug X is equally efficacious to drug Y. drug X is more potent than drug Y. both drug X and drug Y produce a 100% response, but drug X reaches that response at a lower dose. Those curves positioned to the left are more potent than those positioned to the right. drug Z is more potent than drug Y, an ...
February 2007 Toxtidbits
February 2007 Toxtidbits

... dietary supplements are also often adulterated with other drugs, sometimes containing prescription drugs not listed on the label. Some of these undisclosed drugs can result in toxicity from high doses or drug interactions. Report all cases of suspected adulterated drugs to the Maryland Poison Center ...
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Neuropharmacology

Neuropharmacology is the study of how drugs affect cellular function in the nervous system, and the neural mechanisms through which they influence behavior. There are two main branches of neuropharmacology: behavioral and molecular. Behavioral neuropharmacology focuses on the study of how drugs affect human behavior (neuropsychopharmacology), including the study of how drug dependence and addiction affect the human brain. Molecular neuropharmacology involves the study of neurons and their neurochemical interactions, with the overall goal of developing drugs that have beneficial effects on neurological function. Both of these fields are closely connected, since both are concerned with the interactions of neurotransmitters, neuropeptides, neurohormones, neuromodulators, enzymes, second messengers, co-transporters, ion channels, and receptor proteins in the central and peripheral nervous systems. Studying these interactions, researchers are developing drugs to treat many different neurological disorders, including pain, neurodegenerative diseases such as Parkinson's disease and Alzheimer's disease, psychological disorders, addiction, and many others.
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