Author/Authors :
Mortada, Yassar Department of Pharmacology - Schoolof Medicine - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Joharchi, Khojasteh Department of Pharmacology - Schoolof Medicine - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Zarei, Malek Department of Pharmacology - Schoolof Medicine - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Mansouri, Ardalan Cellular and Molecular Biology Research Center & Department of Pharmacology - school of Medicine - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Jorjani, Masoumeh Department of Pharmacology - Schoolof Medicine - Shahid Beheshti University of Medical Sciences, Tehran, Iran
Abstract :
Neuropathic pain is a complication of inflammation, infection or some diseases such as
diabetes. Opioids are used as a salvage therapy for neuropathic pain but tolerance restricts
their use. In our previous study, we have observed an increase of Nitric Oxide in diabetes and
in morphine tolerance. This study was performed to clarify the role of inducible nitric oxide
synthase, iNOS, and cationic amino acid transporter-2, CAT-2, in these conditions.
Thus male rats were divided into four groups: control, diabetic, morphine tolerated, and
diabetic morphine tolerated. For evaluating tolerance Hot-Plate test was achieved. Molecular
study was performed by real time PCR and Western blotting techniques to compare gene and
protein expressions.
Our findings showed that in diabetic animals, morphine tolerance occurred prior to nondiabetic
rats. In molecular study, the expression of iNOS was increased in the spinal cord
whereas the CAT-2 did not change in diabetic morphine tolerated rats.
It seems that the nitric oxide elevation in diabetic morphine tolerated state is mostly due to
the increase of iNOS in male rats.
Keywords :
Male Rat , Cationic Amino Acid Transporter-2 , Nitric Oxide Synthase , Morphine tolerance , Diabetes