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... Healthy, nonsmoking chronic asthmatic patients (males and females of nonchildbearing potential), aged 18–65 yrs, were enrolled. Patients were required to demonstrate a forced expiratory volume in one second (FEV1, measured in the morning, 8–10 h after the evening dose) 40–80% predicted (after withho ...
Case History - Children`s Hospital of Michigan
Case History - Children`s Hospital of Michigan

Spice/K2 drugs – more than innocent substitutes for marijuana
Spice/K2 drugs – more than innocent substitutes for marijuana

... regulated, new analogues appeared on the market in order to satisfy demand and at the same time to avoid criminalization (Lindigkeit et al., 2009; Hudson and Ramsey, 2011; Dargan et al., 2011; Simolka et al., 2012; Ernst et al., 2012; Langer et al., 2013; Uchiyama et al., 2013). Despite modifications ...
Alpha-2 Adrenergic Regulation of Melatonin Release in Chick
Alpha-2 Adrenergic Regulation of Melatonin Release in Chick

... that alpha adrenoceptors mediate the catecholamine-induced suppression of NAT (Deguchi, 1979b). However, these studies did not characterize the dose dependence, the location, or the subtype of the alpha receptor. Deguchi’s preliminary work on the nature of the adrenergic receptor in the chick pineal ...
PAIN & ANALGESIA
PAIN & ANALGESIA

Serotonergic Manipulations Both Potentiate and Reduce Brain
Serotonergic Manipulations Both Potentiate and Reduce Brain

... raphé (Simon et al. 1976; van der Kooy et al., 1978) maintained self-stimulation behavior that was reduced by PCPA, suggesting that self-stimulation of the raphé nuclei is serotonergically mediated. Response rates for self-stimulation of the hippocampus also were decreased by PCPA administration ( ...
this Outline - Alcohol Medical Scholars Program
this Outline - Alcohol Medical Scholars Program

... 1. Buprenorphine maintenance (at ≥16mg/day) better than placebo and naltrexone re: a. Treatment retention b. ↓Opioid positive urines 2. Buprenorphine versus methadone (Slide 39) a. Both improve outcomes, but methadone with greater patient retention b. Buprenorphine carries benefit of office-based Rx ...
Dopamine and Benzodiazepine-Dependent Mechanisms
Dopamine and Benzodiazepine-Dependent Mechanisms

... paradigm. These discrepant results are likely due to the different paradigms assessing different reinforcing properties associated with alcohol. In addition, germane to alcohol’s reinforcing properties, the a1 (/) mice have also been used to investigate alcohol’s locomotor stimulant actions. Both ...
Neurochemical regulation of pair bonding in male
Neurochemical regulation of pair bonding in male

... An important behavioral characteristic associated with pair bonding is that after mating, prairie voles display a robust preference for the familiar mate versus a conspecific stranger. This preferential association with the familiar mate can be quantified using a partner preference test, first devel ...
IOSR Journal of Pharmacy and Biological Sciences (IOSR-JPBS) e-ISSN: 2278-3008, p-ISSN:2319-7676.
IOSR Journal of Pharmacy and Biological Sciences (IOSR-JPBS) e-ISSN: 2278-3008, p-ISSN:2319-7676.

... Insomnia is a widespread health complaint and the most common sleep disorders that affect people of all ages around the world [1, 2]. About 10-15% of adult population suffers from chronic insomnia, and additional 25-35% has transient or occasional insomnia [3]. The most widely used drugs in the mana ...
HEALTHCARE SECTOR SECONDARY RESEARCH SAMPLE REPORT
HEALTHCARE SECTOR SECONDARY RESEARCH SAMPLE REPORT

... 2nd generation agents are TPO peptide and non-peptide mimetics and TPO agonist antibodies. All bind to TPO receptor but in different ways. Potential concerns with new TPO agents are thrombosis, development of cancer/leukemia, antibody production, marrow fibrosis and rebound effects when treatment is ...
Effects of rimonabant on body weight, glucose control
Effects of rimonabant on body weight, glucose control

... advanced pharmacological approach targets C1 receptors [32]. There are different possible mechanisms by which CB1 receptor antagonists produce their effects on the CB1 receptor. The ligands can be pure competitive antagonists of CB1 receptor activation by endogenously released ECs (neutral antagonis ...
Antidepressant specificity of serotonin transporter suggested by three LeuT–SSRI structures Zheng Zhou
Antidepressant specificity of serotonin transporter suggested by three LeuT–SSRI structures Zheng Zhou

... lower affinity than to their principal target, SERT3,4. The selectivity of SSRIs for SERT is intriguing. Merely one or two different functional group substitutions are sufficient to convert an SSRI into a norepinephrine-reuptake inhibitor (NRI) with higher affinity to NET5–7. It is recognized that b ...
Platelet glycoprotein IIb/IIIa receptor blockade in coronary
Platelet glycoprotein IIb/IIIa receptor blockade in coronary

... Cleveland, Ohio and Durham, North Carolina New strategies for profound inhibition of platelet activity at the injured coronary plaque focus on blockade of the platelet surface membrane glycoprotein IIb/IIIa receptor, which binds circulating fibrinogen or von Willebrand factor and crosslinks platelet ...
Use of Plasma Octreotide Levels to Guide Sandostatin® LAR Dosing
Use of Plasma Octreotide Levels to Guide Sandostatin® LAR Dosing

... in patients on doses as high as 6mg/day, and the octreotide drug trials report IV doses as high as 120mg administered over eight hours without serious ill effects. This safety profile provides the clinician with a great deal of latitude in selecting an appropriate dose for those patients whose sympt ...
EXPLORING THE EFFECTS OF NEWER THREE COMPONENT AMINOBENZYLATED REACTIONS  OF TRIPHENYL IMIDAZOLE MOTIF AS POTENT ANTIMICROBIAL AND ANTI­INFLAMMATORY 
EXPLORING THE EFFECTS OF NEWER THREE COMPONENT AMINOBENZYLATED REACTIONS  OF TRIPHENYL IMIDAZOLE MOTIF AS POTENT ANTIMICROBIAL AND ANTI­INFLAMMATORY 

... compounds  was  compared  with  a  standard  drug  Griseofulvin.  The  results of antimicrobial profile were depicted in Table 2.   In vitro anti­inflammatory activity   The  invitro anti‐inflammatory  activity was evaluated  by  human red  blood  cell  membrane  (HRBC)  stabilisation  method15.  Th ...
III期试验无效。
III期试验无效。

... During stroke and reperfusion, free radicals cause damage, induce inflammation. Excessive inflammatory response not only disturb local blood flow, but also exert direct damage to tissue structure, which is a primary reason for ischemic brain damage. Inflammatory cells (leukocyte, monocyte-macrophage ...
Intravenous Ondansetron as Antiemetic Prophylaxis for
Intravenous Ondansetron as Antiemetic Prophylaxis for

... Table 1 also indicates the American Society of Anesthesiologists’ (ASA) physical status classification for the experimental and control groups. Although p > 0.05, 20% of the cells had expected values less than 5, so the chi-square analysis of the p value could not be trusted, and we performed correc ...
Binding of Imipramine to Phospholipid Bilayers Using
Binding of Imipramine to Phospholipid Bilayers Using

... The tendency to refer to the result of drug-lipid bilayer interaction as “binding” has been subject to discussion because of the general meaning of this term in the classic enzyme-substrate or ligand-receptor interaction studies (Heirwegh et al. 1992). Binding into a bilayer is considered a restrict ...
G-Protein Subunit Isoforms Couple Differentially to Receptors that
G-Protein Subunit Isoforms Couple Differentially to Receptors that

... with stable access resistance were included in the data analysis. The membrane potential was held at ⫺60 mV, and EPSC s were evoked every 20 sec by triggering an unclamped action current with a 1.0 msec depolarizing step. The resultant evoked waveform consisted of a brief stimulus artifact and a lar ...
Corticotropin-Releasing Factor: Physiology, Pharmacology, And
Corticotropin-Releasing Factor: Physiology, Pharmacology, And

... addition, the known members of this neuropeptide receptor family also belong to the superfamily of G-protein coupled receptors; thus far, all have been shown to stimulate adenylate cyclase in response to their respective agonist activation. The CRF1 receptor was cloned first from a human Cushing’s c ...
Inhibiting the breakdown of endogenous opioids and
Inhibiting the breakdown of endogenous opioids and

Guideline for the Management of Postoperative Nausea and Vomiting
Guideline for the Management of Postoperative Nausea and Vomiting

... with the antinauseant property of antihistamines.54–56 Diclectin has been used since the 1950s and is considered to be a safe treatment for nausea and vomiting associated with pregnancy.57 The International Cochrane Collaboration has systematically reviewed randomized trials of Diclectin and conclud ...
Hallucinogenic Drugs
Hallucinogenic Drugs

... williamsii but it is also found in significant quantities in the San Pedro cactus, Trichocereus pachanoi. An average human dose is approximately 400 mg, making it 10 000 times less potent than LSD. Mescaline is a long-lasting hallucinogen, persisting for 12]15 hours. A notable side effect of mescaline ...
s - Clayton State University
s - Clayton State University

... a) Increasing the hydrophilicity of substituents allows the identification of an optimum value for p (Sp = -5). The equation is now parabolic (-0.034 (Sp)2) b) The optimum value of Sp is very low and implies a hydrophilic binding site c) R-5 implies that resonance effects are important at position 5 ...
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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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