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Serotonergic Modulation of Rat Pineal Gland Activity: In Vivo
Serotonergic Modulation of Rat Pineal Gland Activity: In Vivo

... studies reported that 5-HT concentrations in the pineal, the highest in the brain, undergo circadian fluctuations, which parallel extracellular 5-HT levels (Young and Anderson, 1982; Azekawa et al., 1991), and it was demonstrated that 5-HT is secreted from the gland in response to noradrenergic stim ...
Volume 48 Number 4
Volume 48 Number 4

... Our membership is also growing; this year we’ve recruited almost 500 new members, 350 of which are new student members. Next year, we hope to continue this growth and encourage more interest in pharmacology and the Society. Centennial Celebration: This year we have also begun preparations for ASPET’ ...
Simultaneous Inhibition of Fatty Acid Amide Hydrolase and
Simultaneous Inhibition of Fatty Acid Amide Hydrolase and

III期试验无效。
III期试验无效。

... ATP is the main energy source of the brain, which is produced by oxidation-phosphorylation and glycolysis. The weight of the brain accounts for 2% of the body weight, the volume of CBF accounts for 15%~20% of the output, while its energy utilization,cell integration account for 40% and its nerve ...
FORMULATION DEVELOPMENT, OPTIMIZATION AND IN-VITRO RELEAS KINETIC STUDY ON
FORMULATION DEVELOPMENT, OPTIMIZATION AND IN-VITRO RELEAS KINETIC STUDY ON

... Acetate, Isopropyl Alcohol (IPA) were procured from S.D Fine Chemicals, Alpha Galactosidase, and Galactomannase were procured from Deer Land Enzymes U.S. All ingredients used were of AR or GR grade and were used as such without further processing. Double distilled water was used where ever required. ...
SHEET L.12 SLIDE 4(Strategies to reduce medication
SHEET L.12 SLIDE 4(Strategies to reduce medication

...  The slide contains an example of guideline protocol The job of this protocol: suppose a new physician, nurse or a pharmacist were hired in a warfarin clinic and they don't have knowledge nor a proper experience about warfarin use, we don't tell them to gain experience by experimenting on people, w ...
Medication errors related to transdermal opioid reporting system
Medication errors related to transdermal opioid reporting system

... two incident reports more than one ME was found which resulted in two additional MEs and a total of 151 MEs were included in the analysis. Of the MEs, 66% (n = 100) concerned fentanyl, 28% (n = 42) unknown substance, and 6% (n = 9) buprenorphine. Of the included MEs 48% (n = 73) were reported during ...
Updating the Beers Criteria for Potentially Inappropriate Medication
Updating the Beers Criteria for Potentially Inappropriate Medication

... steps and was phase 1 of the study. First, we identified literature published since January 1994 in English, describing or analyzing medication use in community-living (ambulatory) older adults and older adults living in nursing homes. From that, we created a table and bibliography. We used MEDLINE, ...
Detoxification Methods of Benzodiazepines Mono
Detoxification Methods of Benzodiazepines Mono

... substitution by an equivalent dose of a long half-life benzodiazepine drug before tapering, especially when patients are difficult to be treated or have low compliance to treatment. However, there is no obvious evidence suggesting the optimum rate of tapering. ...
Neurochemical Neutralization of Methamphetamine With High
Neurochemical Neutralization of Methamphetamine With High

... mediate the addictive effects of METH (Wise, 1996), whereas increased release of NE in both the peripheral and central nervous systems is thought to mediate its cardiovascular effects. The neurotoxic effects of METH on both dopaminergic and serotonergic nerves requires the transport of METH into the ...
Prescribing Information
Prescribing Information

... treatment with KORLYM. In study subjects that experienced declines in HDL-C, levels returned to baseline following discontinuation of drug. The clinical significance of the treatment-related reduction in HDL-C levels in patients with Cushing’s syndrome is not known. In a study of patients with Cushi ...
printable PDF - Edison Investment Research
printable PDF - Edison Investment Research

... temperature and pH). This information can be used to design molecules with better affinity. This is important as drug molecules that are not highly optimised to bind to a particular target often interact with many different receptors or enzymes, which can give unpredictable side-effects and a narrow ...
available now
available now

... increase the dose of the initial drug or add a second drug from one of the classes in recommendation6 (thiazide-type diuretic, CCB, ACEI, or ARB). The clinician should continue to assess BP and adjust the treatment regimen until goal BP is reached. If goal BP cannot be reached with 2 drugs, add and ...
PDF - Journal of Applied Pharmaceutical Science
PDF - Journal of Applied Pharmaceutical Science

... postoperative conditions due to their three major activities, viz., anti-inflammatory, antipyretic, and analgesic. Phenylbutazone, diclofenac, meloxicam and some other NSAIDs are being used as therapeutic measures for pain, inflammation and fever in clinical veterinary medicine. Antiinflammatory eff ...
Introduction to PKPD Continued, Professor Leon Aarons
Introduction to PKPD Continued, Professor Leon Aarons

... The left panel shows the relationship between serum concentration of thiopental and response/ no response to five different clinical stimuli. Each bar indicates the serum thiopental concentration and response to the stimulus applied to an individual patient. The right panel shows the predicted proba ...
Distinct Components of Spatial Learning Revealed by Prior Training
Distinct Components of Spatial Learning Revealed by Prior Training

... Need another experiment to control for amount of AP5 administered!  Why control for this?  Can directly measure if nonspatial pre-training (when spatial learning is disrupting) can account for normal performance in Morris Water Maze ...
highlights of prescribing information full prescribing
highlights of prescribing information full prescribing

... Benicar is 20 mg once daily when used as monotherapy in patients who are not volume-contracted. For patients requiring further reduction in blood pressure after 2 weeks of therapy, the dose of Benicar may be increased to 40 mg. Doses above 40 mg do not appear to have greater effect. Twicedaily dosin ...
2012 פברואר ה
2012 פברואר ה

... oral use. In the event of accidental ingestion of large quantities of GYNODAKTARIN products, an appropriate method of gastric emptying may be used, if considered necessary. See also Section 4.5, Interactions with other medicinal products and other forms of interaction. ...


... or disintegration of tablet content into smaller particles that can dissolve more rapidly than in the absence of disintegrants. Many substances like microcrystalline cellulose, Crospovidone, crosscarmellose sodium, sodium starch glycolate have been used in the formulation of fast disintegrating tabl ...
CNS Drug Design: Balancing Physicochemical
CNS Drug Design: Balancing Physicochemical

... In fact, based on the classic concepts of CNS exposure, 2 should have no in vivo efficacy.27 To explain this phenomenon, several hypotheses, such as glucuronide 2 activation of a new and not yet discovered receptor subtype, have been proposed.24 However, this apparent paradox could also be explained b ...
Sublingual drug delivery system List of contents
Sublingual drug delivery system List of contents

... For a tablet containing a potent drug, three formulation aspects are of special interest. Firstly, incorporation of the necessarily small amounts of a very potent drug could result in poor dose homogeneity, especially if direct compression is desired. Secondly, disintegration should be fast to facil ...
alcohol_physiology
alcohol_physiology

... ◦ Similar to barbiturates and benzodiazepines, it enhances the inhibitory effect of GABA at the GABA-A receptor ◦ At high doses, it blocks the effects of the excitatory transmitter glutamate ◦ It affects dopamine, serotonin, and acetylcholine neurons ...
Treatment of poisoning caused by β
Treatment of poisoning caused by β

... the sarcoplasmic reticulum, and facilitates release of calcium by troponin during diastole. Therapies that promote cAMP formation generally have transient effects in CCB overdose due to the myocyte running out of carbohydrates. (c) Glucagon bypasses β-receptors and acts directly on Gs to stimulate co ...
Thyroid Gland and Anesthetic Management
Thyroid Gland and Anesthetic Management

... Monitoring hypothyroid pts. during anesthesia is intended to facilitate prompt recognition of exaggerated cardiovascular depression, and detection of onset of hypothermia  Consider arterial line for long surgical procedures, or those associated with significant blood loss ...
Anabolic_Steroids-2
Anabolic_Steroids-2

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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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