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Animal models of nociception
D Le Bars, M Gozariu, SW Cadden - Pharmacological reviews, 2001 - Elsevier
The study of pain in awake animals raises ethical, philosophical, and technical problems.
We review the ethical standards for studying pain in animals and emphasize that there are …
We review the ethical standards for studying pain in animals and emphasize that there are …
A summary of mechanistic hypotheses of gabapentin pharmacology
CP Taylor, NS Gee, TZ Su, JD Kocsis, DF Welty… - Epilepsy research, 1998 - Elsevier
Although the cellular mechanisms of pharmacological actions of gabapentin (Neurontin®)
remain incompletely described, several hypotheses have been proposed. It is possible that …
remain incompletely described, several hypotheses have been proposed. It is possible that …
Nociceptive-specific activation of ERK in spinal neurons contributes to pain hypersensitivity
We investigated the involvement of extracellular signal-regulated protein kinases (ERK)
within spinal neurons in producing pain hypersensitivity. Within a minute of an intense …
within spinal neurons in producing pain hypersensitivity. Within a minute of an intense …
Adenosine in the spinal cord and periphery: release and regulation of pain
J Sawynok, XJ Liu - Progress in neurobiology, 2003 - Elsevier
In the central nervous system (CNS), adenosine is an important neuromodulator and
regulates neuronal and non-neuronal cellular function (eg microglia) by actions on …
regulates neuronal and non-neuronal cellular function (eg microglia) by actions on …
Chloride regulation in the pain pathway
Melzack and Wall's Gate Control Theory of Pain laid the theoretical groundwork for a role of
spinal inhibition in endogenous pain control. While the Gate Control Theory was based on …
spinal inhibition in endogenous pain control. While the Gate Control Theory was based on …
The major role of peripheral release of histamine and 5-hydroxytryptamine in formalin-induced nociception
Formalin injected subcutaneously into the paw is a widely used model of pain. This
procedure evokes a short-lasting period of flinching (phase 1) and a long-lasting period of …
procedure evokes a short-lasting period of flinching (phase 1) and a long-lasting period of …
Gabapentin (neurontin) and S‐(+)‐3‐isobutylgaba represent a novel class of selective antihyperalgesic agents
MJ Field, RJ Oles, AS Lewis, S McCleary… - British journal of …, 1997 - Wiley Online Library
1 Gabapentin (neurontin) is a novel antiepileptic agent that binds to the α2δ subunit of
voltage‐dependent calcium channels. The only other compound known to possess affinity …
voltage‐dependent calcium channels. The only other compound known to possess affinity …
d-Methadone blocks morphine tolerance and N-methyl-D-aspartate-induced hyperalgesia
AM Davis, CE Inturrisi - The Journal of Pharmacology and Experimental …, 1999 - Elsevier
Previous in vitro and in vivo studies have determined that the d isomer of methadone has N-
methyl-d-aspartate (NMDA) receptor antagonist activity. The present studies examined the …
methyl-d-aspartate (NMDA) receptor antagonist activity. The present studies examined the …
Peripheral group I metabotropic glutamate receptors modulate nociception in mice
G Bhave, F Karim, SM Carlton, RW Gereau Iv - Nature neuroscience, 2001 - nature.com
The metabotropic glutamate receptors (mGluRs) are found throughout the central nervous
system, where they modulate neuronal excitability and synaptic transmission. Here we …
system, where they modulate neuronal excitability and synaptic transmission. Here we …
Predictive validity of behavioural animal models for chronic pain
OG Berge - British journal of pharmacology, 2011 - Wiley Online Library
Rodent models of chronic pain may elucidate pathophysiological mechanisms and identify
potential drug targets, but whether they predict clinical efficacy of novel compounds is …
potential drug targets, but whether they predict clinical efficacy of novel compounds is …