مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

205
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

144
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

Minocycline through attenuation of oxidative stress and inflammatory response reduces the neuropathic pain in a rat model of chronic constriction injury

Pages

  138-144

Abstract

 Objective(s): Several lines of evidence showed that Minocycline possesses antioxidant and anti-inflammatory properties. This study aimed to demonstRate the effects of Minocycline in Rats subjected to chronic constriction injury (CCI). Materials and Methods: In this study four groups (n = 6– 8) of Rats were used as follows: Sham, CCI, CCI + Minocycline (MIN) 10 mg/Kg (IP) and CCI + MIN 30 mg/Kg (IP). On days 3, 7, 14, and 21 post-surgery hot-plate, acetone, and von Frey tests were carried out. Finally, Motor Nerve Conduction Velocity Evaluation (MNCV) assessment was performed and spinal cords were harvested in order to measure tissue concentRations of TNF_α , IL-1β , Glutathione peroxidase (GPx), Superoxide dismutase (SOD) and Malondialdehyde (MDA). Extent of perineural inflammation and damage around the sciatic nerve was histopathologically evaluated. Results: Our results demonstRated that CCI significantly caused hyperalgesia and allodynia twenty-one days after CCI. MIN attenuated heat hyperalgesia, cold and mechanical allodynia and MNCV in animals. MIN also decreased the levels of TNF_α and IL-1β . Antioxidative enzymes (SOD, MDA, and GPx) were restored following MIN treatment. Our findings showed that MIN decreased perineural inflammation around the sciatic nerve. According to the results, the Neuropathic pain reduced in the CCI hyperalgesia model using 30 mg/kg of Minocycline. Conclusion: It is suggested that antinociceptive effects of Minocycline might be mediated through the inhibition of Inflammatory response and attenuation of Oxidative stress.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    ABBASZADEH, ABOLFAZL, DARABI, SAEIDEH, HASANVAND, AMIN, Amini Khoei, Hossein, Abbasnezhad, Amir, CHOGHAKHORI, RAZIEH, & AALIEHPOUR, ASGHAR. (2018). Minocycline through attenuation of oxidative stress and inflammatory response reduces the neuropathic pain in a rat model of chronic constriction injury. IRANIAN JOURNAL OF BASIC MEDICAL SCIENCES, 21(2), 138-144. SID. https://sid.ir/paper/720689/en

    Vancouver: Copy

    ABBASZADEH ABOLFAZL, DARABI SAEIDEH, HASANVAND AMIN, Amini Khoei Hossein, Abbasnezhad Amir, CHOGHAKHORI RAZIEH, AALIEHPOUR ASGHAR. Minocycline through attenuation of oxidative stress and inflammatory response reduces the neuropathic pain in a rat model of chronic constriction injury. IRANIAN JOURNAL OF BASIC MEDICAL SCIENCES[Internet]. 2018;21(2):138-144. Available from: https://sid.ir/paper/720689/en

    IEEE: Copy

    ABOLFAZL ABBASZADEH, SAEIDEH DARABI, AMIN HASANVAND, Hossein Amini Khoei, Amir Abbasnezhad, RAZIEH CHOGHAKHORI, and ASGHAR AALIEHPOUR, “Minocycline through attenuation of oxidative stress and inflammatory response reduces the neuropathic pain in a rat model of chronic constriction injury,” IRANIAN JOURNAL OF BASIC MEDICAL SCIENCES, vol. 21, no. 2, pp. 138–144, 2018, [Online]. Available: https://sid.ir/paper/720689/en

    Related Journal Papers

  • No record.
  • Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button