introduction: previous studies have shown that the basolateral amygdale (bla) is rich of cb1 cannabinoid receptors and involved in cannabinoid-induced antinociception. also, it seems that there are functional interactions between the cannabinoid cb1 and opioid receptors in the process of sensitization to opiates. in the present study, we tried to examine the role of intra-bla cannabinoid recept...

Background and Purpose New remedies are required for the treatment of neuropathic pain due to insufficient efficacy available therapies. This study provides a novel approach develop painkillers chronic treatment. Experimental Approach The rat formalin test spinal nerve ligation model were used evaluate antinociception protopanaxadiol. Primary cell cultures, immunofluorescence staining, gene pro...

BACKGROUND The clinical benefits of opioid drugs are counteracted by the development of tolerance and addiction. We provide in vivo evidence for the involvement of G protein-coupled receptor kinases (GRKs) in opioid dependence in addition to their roles in agonist-selective mu-opioid receptor (MOR) phosphorylation. METHODS In vivo MOR phosphorylation was examined by immunoprecipitation and na...

The amygdala is a forebrain region, which is known as a modulator of pain sensation. The amygdala, particularly the central nucleus, has high concentrations of enkephalins relative to dynorphins and has high concentrations of opioid receptors. We here studied the role of central nuclei of amygdala in morphine antinociception. Methods: In this study, we used 130 male Wistar rats (200- 250g). Bil...

Introduction: The antinociceptive effect of morphine is, in part, mediated through the activation of a descending pathway. One of the major components of this pathway is the nucleus raphe magnus (NRM). Our previous study demonstrated the involvement of NRM in the analgesic effect of morphine microinjected into the nucleus cuneiformis (NCF) in a descending manner. The aim of the current study...

In earlier studies, it was shown that male rats were considerably more sensitive to the antinociceptive properties of morphine than females in several antinociceptive assays. The purpose of our studies was to examine whether these male-female differences might be due to differences in the blood and brain levels of morphine attained after its s.c. injection rather than to intrinsic differences i...

previous studies have shown that the extract of papaver rhoeas reduces morphine dependence, locomotor activity and reward. in present study, the effects of hydro-alcohol extract of papaver rhoeas on the tolerance to analgesic effects of morphine in mice have been investigated using tail flick method. subcutaneous (s.c.) administration of morphine (1, 2, 5 and 10 mg/kg) induced analgesia. howeve...

Opiates are powerful drugs to treat severe pain, and act via mu opioid receptors distributed throughout the nervous system. Their clinical use is hampered by centrally-mediated adverse effects, including nausea or respiratory depression. Here we used a genetic approach to investigate the potential of peripheral mu opioid receptors as targets for pain treatment. We generated conditional knockout...

The possible characteristics of spinal interaction between sildenafil (phosphodiesterase 5 inhibitor) and morphine on formalin-induced nociception in rats was examined. Then the role of the opioid receptor in the effect of sildenafil was further investigated. Catheters were inserted into the intrathecal space of male Sprague-Dawley rats. For induction of pain, 50 microL of 5% formalin solution ...

Several studies have demonstrated that nitric oxide (NO) is involved in hyperalgesia induced by NMDA activity in Morphine tolerance and NO synthase inhibitors can attenuate hyperalgesia in morphine tolerance. In addition, one of the possible mechanisms in morphine tolerance is reduction of GABA inhibitory effect. For this reason, we used GABA agonists (muscimol and baclofen) to investigate the ...