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Novel psychoactive substances of interest for psychiatry
Novel psychoactive substances of interest for psychiatry

... are also available (10-12). Within any given “Spice” package, usually a range of different SC molecules (13) and/ or further psychoactives (14-20) can be identified. Batches of the same brand may possess highly variable SC concentrations (21). It is likely that a few hundreds of SC molecules are cur ...
Opioid and Cannabinoid Modulation of Precipitated Withdrawal in
Opioid and Cannabinoid Modulation of Precipitated Withdrawal in

... Downloaded from jpet.aspetjournals.org at ASPET Journals on June 18, 2017 ...
Serotonin or 5-hydroxytryptamine
Serotonin or 5-hydroxytryptamine

... treatment; not recommended for patients with coronary vascular disease risk. • formulations: subcutaneous injection, oral, nasal spray • selective serotonin-receptor agonist (short duration of action) • probably more effective than ergotamine for management of acute migraine attacks (relief: 10 to 1 ...
Antidepressant drugs - Dr Lynch
Antidepressant drugs - Dr Lynch

... Symptoms: Neurological (confusion, agitation, coma), Neuromuscular (rigidity, tremors, myoclonus, hyperreflexia), Autonomic (hyperthermia, tachycardia, hyper/hypotension, GI upset) ...
Depression and Suicide
Depression and Suicide

... Symptoms: Neurological (confusion, agitation, coma), Neuromuscular (rigidity, tremors, myoclonus, hyperreflexia), Autonomic (hyperthermia, tachycardia, hyper/hypotension, GI upset) ...
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Pharm 22, 23- Drugs for Affective Disorders Depression
Pharm 22, 23- Drugs for Affective Disorders Depression

...  Injection of norepinephrine, epinephrine or dopamine may be successful in treating priapism  In approximately one-third of the cases reported, surgical intervention was required  in a portion of these cases, permanent impairment of erectile function or impotence resulted  WARN all men of slow d ...
Control Mechanisms of the GI Tract
Control Mechanisms of the GI Tract

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Opioid Presentation pt2(updated) [Read
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... Sedation is a better indicator and should be monitored using a sedation score. This method has limitations if a patient who is deeply sedated is assessed as being in “normal sleep.” “Normal sleep” means patient is asleep but rousable. (eg ...
A fatty acid in the MCT ketogenic diet for epilepsy treatment blocks
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2015 PK and PD
2015 PK and PD

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Simultaneous Inhibition of Fatty Acid Amide Hydrolase and
Simultaneous Inhibition of Fatty Acid Amide Hydrolase and

... Response rate was averaged (6 S.E.M.) among mice and plotted as a function of dose. Response rate for an individual mouse was calculated by expressing the response rate during a test as a percentage of control; the control response rate was defined as the average response rate for the five preceding ...
Chapter 18 Opioid Analgesics
Chapter 18 Opioid Analgesics

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Pharmacology Study Guide – Test 2
Pharmacology Study Guide – Test 2

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Chronic WIN55,212-2 elicits sustained and conditioned increases in
Chronic WIN55,212-2 elicits sustained and conditioned increases in

... and pathways of the brain, which are collectively known as brain reward systems. In most cases, these drugs also yield reinforcing and rewarding effects in experimental animals, as assessed by relevant animal models, such as self-administration, conditioned place preference and intracranial self-sti ...
Opioid Pharmacology Definitions 1. Opium – a mixture of alkaloids
Opioid Pharmacology Definitions 1. Opium – a mixture of alkaloids

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Antipsychotics - Yorkshire and the Humber Deanery
Antipsychotics - Yorkshire and the Humber Deanery

... atypicals, greatest in those with dementia and within first month of starting treatment and with higher doses ...
Subtype-selective GABAA receptor mimetics—novel
Subtype-selective GABAA receptor mimetics—novel

... least in mice and rats. The two pertinent questions at present are, can other unwanted effects besides sedation also be avoided with subtype-selective (or partial) agonists and does the concept of a benzodiazepine-mediated antihyperalgesia also work in humans. Both questions are at present difficult ...
Sedation & Analgesia - Pediatric Critical Care Education
Sedation & Analgesia - Pediatric Critical Care Education

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schizophrenia
schizophrenia

... chlorpromazine and thioridazine, studies showed that only a few atypical medications (clozapine, olanzapine, and risperidone) caused fewer movement disorders, but the low-potency drugs also tended to induce weight gain and sedation like the atypicals. ...
PSY650-Antipsychotics-Sedative-Hypnotics
PSY650-Antipsychotics-Sedative-Hypnotics

... Mechanisms of Action • Classicals are usually D2 and D2-like receptor antagonists • Atypicals antagonize D2-like receptors plus some 5-HTa action – LSD – The serotonin hypothesis of negative symptoms ...
Drugs acting on the uterus
Drugs acting on the uterus

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Narcan Overview - Telco House Bed & Breakfast
Narcan Overview - Telco House Bed & Breakfast

... push; repeat as indicated (per protocol) SC; repeat as indicated (per protocol) ...
Basic concepts in clinical pharmacology
Basic concepts in clinical pharmacology

... 1. You are the OOH drug information scientist / pharmacist / GP / on-call officer for the pharmaceutical company / nurse / etc. 2. The (male) patient has a longstanding history of kidney stones. They are usually small, they usually pass within 48 h, and the patient has been responsibly using 10 mg m ...
Effects of different drugs of different - Sun Yat
Effects of different drugs of different - Sun Yat

... receptor antagonist and the proton pump inhibitor. Being the H2 receptor antagonist,Cimetidine can compete the H2receptors with histamine.Thereby,it can block the histamine’s function of promoting the secretion of gastric acid. Being the proton pump inhibitor, Omeprazole can block the last step of s ...
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Cannabinoid receptor antagonist



The discovery of the endogenous cannabinoid system led to the development of CB1 receptor antagonists. The first cannabinoid receptor antagonist, rimonabant, was described in 1994. Rimonabant blocks the CB1 receptor selectively and it has been shown to decrease food intake and regulate body-weight gain. The prevalence of obesity worldwide is increasing dramatically and has a great impact on public health. The lack of efficient and well-tolerated drugs to cure obesity has led to an increased interest in research and development of cannabinoid antagonists. Cannabidiol, a naturally occurring cannabinoid, is a non-competitive CB1/2 antagonist.
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