Pro-inflammatory cytokines play a key role in the inflammatory response and contributing to producing local hyperalgesia. It is known that pentoxifylline inhibits inflammatory cytokine production. Therefore, the aim of this study was to find out, using a behavioural test and neuronal Fos expression, if this drug had some antinociceptive effect decreasing nociresponsive neuron activation in the spinal cord after nociceptive inflammation (injection of formalin in the hind paw). Our data showed that formalin induced a great number of Fos-positive neurons in the dorsal horn of the lumbar spinal cord mainly in the ipsilateral I and II laminae. The local pre-treatment with pentoxifylline before the formalin injection, decreased the nociceptive re...
SUMMARY: Oxytocin (OXT) inhibits pain transmission at the spinal cord level by activating oxytocin r...
1 Although previous reports have suggested that the sigma 1 (s1) receptor may be involved in pain s...
Activated glia are a source of substances known to enhance pain, including centrally synthesized pro...
A hind paw subcutaneous injection of dilute formalin (1.25%, 0.1ml), a model of inflammatory pain, w...
Although the formalin test is a widely used model of persistent pain, the primary afferent fiber typ...
Although the formalin test is a widely used model of persistent pain, the primary afferent fiber typ...
The formalin test produces 2 well known acute phases of nociceptive behavior Recently we have shown ...
To determine whether initial nociceptive inputs caused by subcutaneous injection of formalin into th...
The study of neuroplasticity following noxious stimulation has reinforced the clinical concept of pr...
AbstractThe purpose of this study was to investigate the contribution of spinal nitric oxide (NO) to...
T-type Ca2+ channels have been implicated in the induction of long-term potentiation, a synaptic pla...
It is generally accepted that the phospholipase-A(2) -cyclooxygenase-prostanoids-cascade mediates sp...
Palmitoylethanolamide (PEA) is an endogenous cannabinoid-like compound in the central nervous system...
Cannabinoids, such as anandamide, are involved in pain transmission. We evaluated the effects of AM4...
BACKGROUND: The status of neuropathic pain alters the responsiveness to formalin injection in rats. ...
SUMMARY: Oxytocin (OXT) inhibits pain transmission at the spinal cord level by activating oxytocin r...
1 Although previous reports have suggested that the sigma 1 (s1) receptor may be involved in pain s...
Activated glia are a source of substances known to enhance pain, including centrally synthesized pro...
A hind paw subcutaneous injection of dilute formalin (1.25%, 0.1ml), a model of inflammatory pain, w...
Although the formalin test is a widely used model of persistent pain, the primary afferent fiber typ...
Although the formalin test is a widely used model of persistent pain, the primary afferent fiber typ...
The formalin test produces 2 well known acute phases of nociceptive behavior Recently we have shown ...
To determine whether initial nociceptive inputs caused by subcutaneous injection of formalin into th...
The study of neuroplasticity following noxious stimulation has reinforced the clinical concept of pr...
AbstractThe purpose of this study was to investigate the contribution of spinal nitric oxide (NO) to...
T-type Ca2+ channels have been implicated in the induction of long-term potentiation, a synaptic pla...
It is generally accepted that the phospholipase-A(2) -cyclooxygenase-prostanoids-cascade mediates sp...
Palmitoylethanolamide (PEA) is an endogenous cannabinoid-like compound in the central nervous system...
Cannabinoids, such as anandamide, are involved in pain transmission. We evaluated the effects of AM4...
BACKGROUND: The status of neuropathic pain alters the responsiveness to formalin injection in rats. ...
SUMMARY: Oxytocin (OXT) inhibits pain transmission at the spinal cord level by activating oxytocin r...
1 Although previous reports have suggested that the sigma 1 (s1) receptor may be involved in pain s...
Activated glia are a source of substances known to enhance pain, including centrally synthesized pro...