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Effects of psilocybin on hippocampal neurogenesis and extinction of
Effects of psilocybin on hippocampal neurogenesis and extinction of

... p  = 0.34]. Notably, there was a significant effect of Trial [F(1,90) = 105.85, p < 0.0001], indicating that mice spent significantly more time freezing after the CS–US pairings during the context test compared to habituation baseline. These data show that all mice learned to fear the context in whi ...
PDF of Novartis pipeline
PDF of Novartis pipeline

Document
Document

A role for D2 but not D1 dopamine receptors in the cross
A role for D2 but not D1 dopamine receptors in the cross

... because the striatum is made up of separate populations of medium spiny neurons expressing either D1-like or D2-like dopamine receptors, selective agonists and antagonists were used to define the selective involvement of these receptor subtypes. ...
Companion animal praCtiCe Medical management of
Companion animal praCtiCe Medical management of

... thought to be the main chemical transmitter involved in vomiting. Maropitant (Cerenia; Pfizer) (Fig 4) is a NK-1 receptor antagonist, which prevents substance P from binding to neurokinin receptors. NK-1 receptors are located throughout the body, including the fundus of the stomach, the medullary vo ...
Statins induced myopathy
Statins induced myopathy

... - Reduction of endogenous intracellular cholesterol leads to increase in gene expression of LDL-R. - Increase hepatic uptake of LDL and its precursors such as IDL and VLDL. - inhibit hepatic syntesis of apolipoprotein B-100 - Increase in apolipoprotein E receptor productions ...
Phase `0` Clinical Trials or Exploratory Investigational New Drug
Phase `0` Clinical Trials or Exploratory Investigational New Drug

... administration continues if clinical benefit which means even phase ‘0’ trials don’t have any therapeutic intention. With the ultrasensitive accelerator mass spectrometry (AMS) it was possible to carry out clinical trials in human using small dose to obtained pharmacokinetic data.16,17,18 ...
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АНАЛГЕЗИВНІ ЗАСОБИ
АНАЛГЕЗИВНІ ЗАСОБИ

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PDF full-Text
PDF full-Text

... Single-blind, placebo-controlled oral provocation tests were performed with lansoprazole, omeprazole, famotidine, and ranitidine at 30-minute intervals in fractionated dosages until the full therapeutic dose was reached or there was an adverse reaction (hypotension, shortness of breath, difficulty i ...
  CLINTON E. CANAL, PH.D. CURRICULUM VITAE
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in silico predictive model to determine vector
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WEB-TRIAGE: An application for patient registration in phase I dose-escalation studies
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... Adult male Sprague-Dawley rats (Charles River) weighing 320-390g were used. All procedures were approved by the Institutional Animal Care and Use Committee of the University of Pennsylvania. ...
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http://www.utdallas.edu/~tres/papers/thompson&disterhoft.97a.pdf
http://www.utdallas.edu/~tres/papers/thompson&disterhoft.97a.pdf

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GPIIb - IIIa - ICU education
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The Value of Phenotypic Screening to Drug Discovery
The Value of Phenotypic Screening to Drug Discovery

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D-Cycloserine in Neuropsychiatric Diseases: A

... central active mechanism to be a selective partial NMDA agonist acting at the glycine-binding site of the NMDA receptor. It was postulated, and later proven on slice preparations, that DCS influences long-term potentiation (LTP), a neuronal mechanism thought to be relevant for learning (Watanabe et  ...
the pharmacokinetics of a thiazole benzenesulfonamide
the pharmacokinetics of a thiazole benzenesulfonamide

... in the femoral artery, femoral vein, and portal vein. Rats were dosed with 1 by 30 min infusion via the femoral vein (N ⫽ 3) or via the portal vein (N ⫽ 3) at 0.2 mg/kg (1 ml/kg; 0.2 mg/ml) in a vehicle consisting of ethanol/polyethylene glycol 400/0.9% saline (20:60:20, v/v/v). Three rats were dose ...
Drugs affecting the respiratory system - Lectures
Drugs affecting the respiratory system - Lectures

...  Difficult to identify whether cause is viral or bacterial  Treatment is “empiric therapy,” treating the most likely cause  Antivirals and antibiotics may be used, but a definite viral or bacterial cause may not be easily identified ...
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NK1 receptor antagonist

Neurokinin 1 (NK1) antagonists are a novel class of medications that possesses unique antidepressant, anxiolytic, and antiemetic properties. The discovery of neurokinin 1 (NK1) receptor antagonists was a turning point in the prevention of nausea and vomiting associated with cancer chemotherapy.An example of a drug in this class is aprepitant. Chemotherapy-induced emesis appears to consist of acute and delayed phases. So far, the acute phase emesis responds to 5-HT3 antagonists while the delayed phase remains difficult to control. The discovery and development of NK1 receptor antagonists have elicited antiemetic effect in both acute and especially in delayed phases of emesis.The first registered clinical use of NK1 receptor antagonists was the treatment of emesis, associated with cancer chemotherapy.
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