نتایج جستجو برای: chronic morphine

تعداد نتایج: 510067  

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 1996
M T Berhow N Hiroi E J Nestler

Local infusion of brain-derived neurotrophic factor (BDNF) into the ventral tegmental area (VTA) can prevent and reverse the ability of chronic morphine or cocaine exposure to induce tyrosine hydroxylase (TH) in this brain region. The present study examined a possible role for extracellular signal regulated kinases (ERKs), the major effector for BDNF and related neurotrophins, in morphine and c...

2016
Wen-Ling Dai Feng Xiong Bing Yan Zheng-Yu Cao Wen-Tao Liu Ji-Hua Liu Bo-Yang Yu

Tolerance induced by morphine remains a major unresolved problem and significantly limits its clinical use. Recent evidences have indicated that dopamine D2 receptor (D2DR) is likely to be involved in morphine-induced antinociceptive tolerance. However, its exact effect and molecular mechanism remain unknown. In this study we examined the effect of D2DR on morphine antinociceptive tolerance in ...

Journal: :European journal of pharmacology 2012
Yunjing Bai Yonghua Peng Jing Liang Xigeng Zheng

The transition to addiction often involves a gradual process of escalated drug intake. The purpose of the present study was to characterize neuronal activation in the ventral tegmental area (VTA) and substantia nigra (SN) following chronic escalating-dose morphine exposure (days 1-7, 2 mg/kg/d; days 8-21, beginning at 10 mg/kg/d, increasing by 2 mg/kg/d), with steady-dose morphine (2 mg/kg/d, i...

2016
Leila Satarian Mohammad Javan Fereshteh Motamedi

Introduction: Stress inhibits the development of tolerance to morphine analgesia via activating HypothalamicPituitary-Adrenal (HPA) axis. Modified catecholamine systems have been reported following morphine tolerance development. In the current study we tried to evaluate changes in the gene expression levels for MAO-A, MAO-B, COMT and thyrosine hydroxylase (TyH) enzymes following chronic pain, ...

Journal: :American journal of physiology. Cell physiology 2012
Gracious R Ross Aravind R Gade William L Dewey Hamid I Akbarali

Opiates are potent analgesics for moderate to severe pain. Paradoxically, patients under chronic opiates have reported hypernociception, the mechanisms of which are unknown. Using standard patch-clamp technique, we examined the excitability, biophysical properties of tetrodotoxin-resistant (TTX-R) Na(+) and transient receptor potential vanilloid 1 (TRPV1) channels of dorsal root ganglia neurons...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2003
Venetia Zachariou Dan Georgescu Nick Sanchez Zia Rahman Ralph DiLeone Olivier Berton Rachael L Neve Laura J Sim-Selley Dana E Selley Stephen J Gold Eric J Nestler

Regulators of G protein signaling (RGS) are a family of proteins known to accelerate termination of effector stimulation after G protein receptor activation. RGS9-2, a brain-specific splice variant of the RGS9 gene, is highly enriched in striatum and also expressed at much lower levels in periaqueductal gray and spinal cord, structures known to mediate various actions of morphine and other opia...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2005
Colleen A McClung Eric J Nestler Venetia Zachariou

Morphine dependence is associated with long-term adaptive changes in the brain that involve gene expression. Different behavioral effects of morphine are mediated by different brain regions, for example, the locus ceruleus (LC), a noradrenergic nucleus, is implicated in physical dependence and withdrawal, whereas the ventral tegmental area (VTA), a dopaminergic nucleus, contributes to rewarding...

Journal: :The Journal of pharmacology and experimental therapeutics 2004
Daniella L Muller Ellen M Unterwald

In vitro evidence suggests that extracellular signal-regulated protein kinases (ERKs) and Akt (also referred to as protein kinase B) are among the myriad of intracellular signaling molecules regulated by opioid receptors. The present study examined the regulation of ERK and Akt activation in the nucleus accumbens and caudate putamen following acute and chronic morphine administration in the rat...

Journal: :The Journal of pharmacology and experimental therapeutics 1997
H N Bhargava J T Bian S Kumar

The effects of twice-daily injections of L-arginine or D-arginine (200 mg/kg i.p.) for 4 days on morphine-induced antinociception, brain nitric oxide synthase activity and brain and serum distribution of morphine and brain mu-opioid receptors labeled with [3H][D-Ala2,MePhe4,Gly5-ol]enkephalin were determined in male Swiss-Webster mice. Chronic treatment with L-arginine, but not D-arginine, decr...

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 ...

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