نتایج جستجو برای: morphine potency

تعداد نتایج: 40586  

Journal: :The Journal of pharmacology and experimental therapeutics 2006
Shinjae Chung Sigrun Pohl Joanne Zeng Olivier Civelli Rainer K Reinscheid

The neuropeptide orphanin FQ/nociceptin (OFQ/N) has been shown to counteract several effects of endogenous and exogenous opioids, and it has been proposed as an opioid-modulating agent involved in the development of morphine tolerance and dependence. However, conflicting results have been obtained from animal models using different protocols to induce morphine tolerance. Here, we report that bo...

Journal: :Pain management 2017
Sedigheh Nadri Hormoz Mahmoudvand Sepideh Vahabi

AIM This research was carried out to compare magnesium sulfate (MgSO4) with isotonic saline in terms of pain control after herniorrhaphy. PATIENTS & METHODS A randomized double-blind study, in which the patients were blind to all. A total of 100 patients who were candidates of herniorrhaphy were randomized into two groups: experimental and control (50 patients in each). Anesthesia was induced...

Journal: :The Journal of pharmacology and experimental therapeutics 2006
Jan Rodriguez Parkitna Ilona Obara Agnieszka Wawrzczak-Bargiela Wioletta Makuch Barbara Przewlocka Ryszard Przewlocki

Repeated administration of morphine is associated with the development of tolerance, yet the mechanism underlying this phenomenon is still poorly understood. Recent evidence implicating glycogen synthase kinase 3 (GSK3) in opioid receptor signaling pathways has prompted us to investigate its role in morphine tolerance. Administration of 10 mg/kg morphine i.p. to Wistar rats twice daily for 8 da...

Journal: :Anesthesiology 2000
M M Puig W Warner O Pol

BACKGROUND Morphine and clonidine show synergy or antagonism inhibiting gastrointestinal transit depending on their proportion and level of effect. Their interaction during morphine tolerance and intestinal inflammation were assessed. METHODS Gastrointestinal transit in mice was evaluated with charcoal and antitransit effects expressed as percent mean values +/- SEM. Tolerance was induced wit...

Journal: :AANA journal 1983
J Yanulevich

Nalbuphine hydrochloride is a relatively new agonist-antagonist drug structurally related to the potent narcotic, oxymorphone (Numorphan®), and the potent narcotic antagonist, naloxone (Narcan®). (Figure 1.) Nalbuphine has a potency equivalent to morphine sulphate and meperidine (10 mg morphine sulphate and 75 mg meperidine being equivalent to 20 mg nalbuphine), 1 with an abuse potential which ...

Bagheri, Seyyed Majid, Dashti-R, Mohammad Hossein , Nazemian Yazdu, Mohammadreza, Qane, Mohammad Davud , Shefaie, Farzane,

Backgrounds and Aims: Cinnamomum Zeylanicum is a medicinal herb used in Iranian traditional medicine as an analgesic spice, which its analgesic effect has been experimentally confirmed. Thus, this study was conducted to compare the antinociceptive effect of cinnamon essential oil (CEO) with those of Morphine and Diclofenac in mice. Materials and Methods: 80 male albino mice were selected and...

Journal: :Indian journal of physiology and pharmacology 1997
A S Mahajan K Chakrabarty T K Mishra A S Chakrabarty

There are controversial reports on the effect of diabetes on the pain threshold. We used male Wistar rats to see the effect of streptozotocin induced diabetes on the tail flick, vocalisation and vocalisation after discharge responses. These represent the spinal, lower brain stem and hypothalamic responses respectively. The effect of morphine in these parameters was studied for both the control ...

Journal: :مجله بین المللی علوم آزمایشگاهی 0
mohammad hossein dashti-r mohammad davud qane farzane shefaie mohammadreza nazemian yazdu seyyed majid bagheri

backgrounds and aims: cinnamomum zeylanicum is a medicinal herb used in iranian traditional medicine as an analgesic spice, which its analgesic effect has been experimentally confirmed. thus, this study was conducted to compare the antinociceptive effect of cinnamon essential oil (ceo) with those of morphine and diclofenac in mice. materials and methods: 80 male albino mice were selected and ra...

Journal: :The Journal of pharmacology and experimental therapeutics 2006
M C Holden Ko Mary F Divin Heeseung Lee James H Woods John R Traynor

6beta-Naltrexol is the major metabolite of the opioid receptor antagonist, naltrexone, in humans. However, there are no functional studies of 6beta-naltrexol in primates. The aim of this study was to compare the in vitro and in vivo potencies of naltrexone and 6beta-naltrexol in rhesus monkeys. Affinity and potency were determined using radioligand displacement and stimulation of 5'-O-(3-[(35)S...

Journal: :American journal of physiology. Regulatory, integrative and comparative physiology 2006
Xiaoya Wang Richard J Traub Anne Z Murphy

Central or systemic administration of agonists directed at the mu or delta opiate receptors generally produce a greater degree of analgesia in males than in females. To date, most studies examining sex-based differences in opioid analgesia have used acute noxious stimuli (i.e., tail-flick and hot plate test); thus the potential dimorphic response of centrally acting opiates in the alleviation o...

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