“Role of the Phosphodiesterase-5 Inhibitor (Tadalafil) In Morphine Induced Analgesia in Rats” Summary

ثبت نشده
چکیده

The current study addressed two important concerns, one pertinent to the impact of PDE-5 inhibitor (tadalafil) on morphine-induced analgesia and the second relevant to its influence on morphine-induced oxidative stress in two different pain models, the the tail-flick test (representing an acute thermal phasic pain model ) and the formalin test (representing an inflammatory tonic pain model ). This study was performed in adult male albino rats treated with morphine in the absence or presence of tadalafil, a PDE-5 inhibitor, L-NAME, a non selective nitric oxide synthase inhibitor and methylene blue, a guanylyl cyclase inhibitor, to investigate the effect of these interventions on morphine-induced analgesia and oxidative stress. The former was evaluated through measurement of tail-flick latencies (represented as MPE) and hind paw flinches (represented as AUC) in both tail flick test and formalin test, respectively. The latter was detected through assessment of various biochemical parameters in the rat liver homogenates including GSH, total GPX activity and MDA.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Low Dose Morphine Enhances Morphine Antinociception Effects in the Animals Pretreated with Selective and Non-Selective Phosphodiestrase Inhibitors

       In this study, we investigated the interactive effects of intraperitoneal (i.p.) injections of three different phosphodiesterase inhibitors (PDEIs) on morphine-induced analgesia in mice using tail-flick method. Subcutaneous administration of morphine (1, 3 and 6 mg/kg) caused significant antinociceptive effects in a dose dependent manner. Administration of pentoxifylline (12.5, 25, 50 an...

متن کامل

Study on the possible similar mechanism of ultra low dose-induced hyperalgesia and development of tolerance to analgesia in male rats: an study based on the role of Gs signaling pathway

Introduction: Ultra low dose (ULD) morphine induces hyperalgesia which is mediated by excitatory Gscoupled opioid receptors. This study was designed to investigate the development of tolerance to hyperalgesic effect of morphine. Also we attempt to seek possible similarity, in view of Gs proteins, between hyperalgesic effect of ULD and hyperalgesic effect after tolerance to HD. Method: Male ...

متن کامل

Possible role for integrins in the development of tolerance to the analgesic effect of morphine in male rats

There is some evidence supporting the reduced activity of integrins following chronic administration of morphine. This reduction might play a role in morphine tolerance development. Manganese binds to the extracellular domain of integrins and makes them to be activated. The effect of integrins activation using manganese on tolerance development to the analgesic effect of morphine was investi...

متن کامل

Morphine-induced analgesia subsequent to formalin injection in female Wistar rat

Background and Objectives: Previous studies have shown the antinociceptive effect of morphine in animal models, but the specific anti-pain consequence of the abuse drug in female animals is unclear. The present research showed the morphine antinociception in female Wistar rats using formalin test. Materials and Methods: Subjects were 40 female Wistar rats purchased from Pasteur Institute of Ir...

متن کامل

Effects of intrathecal administration of genipin on pain and morphine induced analgesia in rats

Introduction: Uncoupling protein 2 (UCP2) in the inner mitochondrial membrane changes the activity of KATP channels and the cell excitability, probably by decreasing the ATP production. Given the expression of UCP2 in primary afferent neurons, and the importance of these channels in morphine-induced analgesia, genipin, an UCP2 inhibitor, may affect these processes, when administrated intrath...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2016