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:

347
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

125
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

A POSSIBLE NON-GENOMIC EPILEPTOGENIC PROPERTIES OF ESTRADIOL ATTENUATED BY MK801 AND DNQX IN AMYGDALA KINDLED RATS

Pages

  987-993

Abstract

 Although the epileptogenic properties of estrogens have been widely demonstrated in several models and species, the mechanism (s) by which estrogens can acutely change SEIZURE parameters including after discharge and SEIZURE durationremains to be determined. In the present study, we examined the role of NMDA (N-methyl-D-aspartate), non-NMDA andestrogen receptors in ESTRADIOL BENZOATE (EB) effects on kindled SEIZURE parameters.Different groups of fully kindled MALE RATS received either EB (30 mg /Kg); EB plus MK801 (2 mg/Kg, as NMDA antagonist); DNQX (7.5 mg/Kg); tamoxifen (TAM, 0.1 mg/Kg, as non- NMDA antagonist) or intra-amygdala injection of anisomycine (30 mmol/mL, a protein synthesis inhibitor). Kindled SEIZURE parameters including after discharge duration (ADD) and stage 5 duration (S5D) were determined at 0.25 and 3 h post sesame oil (EB solvent) or EB treatment.While pretreatment with either MK801 or DNQX could block the ADD prolongation induced by EB at 0.25 h, they had no effect on S5D prolongation at 3 h. Moreover, application of anisomycine or TAM had no effect on estradiol induced ADD and S5D prolongation. These results indicate that both NMDA and non-NMDA receptors could be involved in EB induced ADD prolongation. The observed short termnon-estrogenic receptor or protein synthesis dependent effects of EB may provide a non-genomic mechanism for the stimulatory effects of the steroid on SEIZURE activity.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    SABERI, MEHDI, SABERI, FATEMEH, & VESALI MAHMOUD, ROSHANAK. (2014). A POSSIBLE NON-GENOMIC EPILEPTOGENIC PROPERTIES OF ESTRADIOL ATTENUATED BY MK801 AND DNQX IN AMYGDALA KINDLED RATS. IRANIAN JOURNAL OF PHARMACEUTICAL RESEARCH (IJPR), 13(3), 987-993. SID. https://sid.ir/paper/288266/en

    Vancouver: Copy

    SABERI MEHDI, SABERI FATEMEH, VESALI MAHMOUD ROSHANAK. A POSSIBLE NON-GENOMIC EPILEPTOGENIC PROPERTIES OF ESTRADIOL ATTENUATED BY MK801 AND DNQX IN AMYGDALA KINDLED RATS. IRANIAN JOURNAL OF PHARMACEUTICAL RESEARCH (IJPR)[Internet]. 2014;13(3):987-993. Available from: https://sid.ir/paper/288266/en

    IEEE: Copy

    MEHDI SABERI, FATEMEH SABERI, and ROSHANAK VESALI MAHMOUD, “A POSSIBLE NON-GENOMIC EPILEPTOGENIC PROPERTIES OF ESTRADIOL ATTENUATED BY MK801 AND DNQX IN AMYGDALA KINDLED RATS,” IRANIAN JOURNAL OF PHARMACEUTICAL RESEARCH (IJPR), vol. 13, no. 3, pp. 987–993, 2014, [Online]. Available: https://sid.ir/paper/288266/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