نتایج جستجو برای: morphine transport

تعداد نتایج: 288495  

Journal: :Biochemical pharmacology 1974
M J Marks F Medzihradsky

The accumulation of selected CNS drugs by rat leukocytes was previously reported. This paper presents evidence for the transport into leukocytes of additional drugs. Also studied was the inhibition of the latter processes by various structurally related compounds. The markedly rapid and sodium-independent uptakes into rat leukocytes of amphetamine, codeine, methadone and naloxone fulfilled the ...

Journal: :Journal of neurophysiology 2002
James M Brundege John T Williams

There is a growing body of evidence suggesting that the neuromodulator adenosine is involved in drug addiction and withdrawal and that adenosine signaling pathways may offer new targets for therapeutic treatments of addiction. Recent studies have suggested that chronic exposure to drugs of abuse may alter adenosine metabolism in the nucleus accumbens, a brain region critically involved in drug ...

2014
Lucy Sanchez-Covarrubias Lauren M. Slosky Brandon J. Thompson Yifeng Zhang Mei-Li Laracuente Kristin M. DeMarco Patrick T. Ronaldson Thomas P. Davis

Our laboratory has previously demonstrated that peripheral inflammatory pain (PIP), induced by subcutaneous plantar injection of λ-carrageenan, results in increased expression and activity of the ATP-dependent efflux transporter P-glycoprotein (P-gp) that is endogenously expressed at the blood-brain barrier (BBB). The result of increased P-gp functional expression was a significant reduction in...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه صنعتی اصفهان - دانشکده شیمی 1390

abstract venlafaxine, 1–[2–(dimethylamino)–1–(4–methoxyphenyl) ethyl]cyclohexanol hydrochloride is a novel non-tricyclic antidepressant. venlafaxine is a second generation antidepressant drug, has a neuropharmacologic profile distinct from that of existing antidepressants including tricyclic compounds, selective serotonin reuptake inhibitors and monoamine oxidase inhibitors. venlafaxine impart...

Journal: :Vojnosanitetski pregled 2014
Velibor Vasović Sasa Vukmirović Momir Mikov Ivan Mikov Zorana Budakov Nebojsa Stilinović Boris Milijasević

BACKGROUND/AIM It is known that bile acids improve the absorption, bioavailability and pharmacodynamic characteristics of some drugs. Morphine analgesia is produced by activation of opioid receptors within the central nervous system (CNS) at both spinal and supraspinal levels. Since a morphine molecule contains 3 polar groups and therefore hard to transfer through the blood-brain barrier, the a...

Journal: :Pharmacological reports : PR 2013
Bruno Mégarbane Hisham Alhaddad

Wang et al. investigated the analgesic effects of morphine and buprenorphine in patients with histologically confirmed malignant tumors of different kinds at terminal stages in one palliative care unit [12]. They showed that patients with P-glycoprotein (P-gp)+ tumors required a higher morphine dose to achieve a satisfactory analgesic effect assessed using the visual analog scale test, in compa...

Journal: :Anesthesiology 2004
Young Jin Lim Shuqiu Zheng Zhiyi Zuo

BACKGROUND Morphine pretreatment via activation of delta1-opioid receptors induces cardioprotection. In this study, the authors determined whether morphine preconditioning induces ischemic tolerance in neurons. METHODS Cerebellar brain slices from adult Sprague-Dawley rats were incubated with morphine at 0.1-10 microM in the presence or absence of various antagonists for 30 min. They were the...

Journal: :Molecular pharmacology 2013
Lauren M Slosky Brandon J Thompson Lucy Sanchez-Covarrubias Yifeng Zhang Mei-Li Laracuente Todd W Vanderah Patrick T Ronaldson Thomas P Davis

Effective pharmacologic treatment of pain with opioids requires that these drugs attain efficacious concentrations in the central nervous system (CNS). A primary determinant of CNS drug permeation is P-glycoprotein (P-gp), an endogenous blood-brain barrier (BBB) efflux transporter that is involved in brain-to-blood transport of opioid analgesics (i.e., morphine). Recently, the nuclear receptor ...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2011
Muhammad Waqas Sadiq Mehran Salehpour Niklas Forsgard Göran Possnert Margareta Hammarlund-Udenaes

Morphine has been predicted to show nonlinear blood-brain barrier transport at lower concentrations. In this study, we investigated the possibility of separating active influx of morphine from its efflux by using very low morphine concentrations and compared accelerator mass spectrometry (AMS) with liquid chromatography-tandem mass spectrometry (LC-MS/MS) as a method for analyzing microdialysis...

Journal: :Molecular pharmacology 2007
Koen van de Wetering Noam Zelcer Annemieke Kuil Wouter Feddema Michel Hillebrand Maria L H Vlaming Alfred H Schinkel Jos H Beijnen Piet Borst

Glucuronidation is a major hepatic detoxification pathway for endogenous and exogenous compounds, resulting in the intracellular formation of polar metabolites that require specialized transporters for elimination. Multidrug resistance proteins (MRPs) are expressed in the liver and can transport glucuronosyl-conjugates. Using morphine as a model aglycone, we demonstrate that morphine-3-glucuron...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید