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:

293
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:

1

Information Journal Paper

Title

INDUCTION OF APOPTOSIS AND CYTOTOXIC ACTIVITIES OF IRANIAN ORTHODOX BLACK TEA EXTRACT (BTE) USING IN VITRO MODELS

Pages

  255-260

Abstract

 Purpose: Plant-derivate therapeutic agents can perform cancer chemotherapeutic activity through triggering apoptotic cell death. Our aim was to investigate the CYTOTOXIC effects, induction of APOPTOSIS, and the mechanism of cell death of IRANIAN ORTHODOX BLACK TEA EXTRACTs (BTEs) and hydro methanolic purified fractions (40, 60, 80 and 100%) in KB cells (oral squamous cell carcinoma).Methods: In order to analyze the CYTOTOXIC activity of the BTEs, MTT (3- (4, 5- dimetylthiazol-2-yl) -2, 5 diphenyltetrazolium bromide) and Trypan-blue assays were performed in ORAL SQUAMOUS CELL CARCINOMA (KB). Furthermore, the APOPTOSIS inducing action of the extracts was determined by TUNEL, DNA fragmentation and cell death detection analysis.Results: Dichloromethane BTE and hydro methanol fractions (40 and 60%) extract showed no CYTOTOXIC effects; however, hydro methanol crude and hydro methanol fractions of BTE (80 and 100%) significantly inhibited cell growth and viability in a dose and time dependent manner. In addition, Cell death assay, TUNEL, and DNA fragmentation indicated induction of APOPTOSIS by hydro methanol 80 and 100% fractions of BTE in KB cells. Statistical significance was determined by analysis of variance (ANOVA), followed by Duncan test and p value ≤0.05 was considered significant.Conclusion: The results from the present study suggests that the hydro methanol crude and hydro methanol fractions of BTE (80 and 100%) are significant source of compounds with the anti proliferative and CYTOTOXIC activities, and this may be useful for developing potential chemo preventive substances.

Cites

References

  • No record.
  • Cite

    APA: Copy

    AGHBALI, AMIRALA, MORADI ABBASABADI, FARANAK, DELAZAR, ABBAS, VOSOUGH HOSSEINI, SEPIDEH, ZARE SHAHNEH, FATEMEH, BARADARAN, BEHZAD, & JANANI, MARYAM. (2014). INDUCTION OF APOPTOSIS AND CYTOTOXIC ACTIVITIES OF IRANIAN ORTHODOX BLACK TEA EXTRACT (BTE) USING IN VITRO MODELS. ADVANCED PHARMACEUTICAL BULLETIN, 4(3), 255-260. SID. https://sid.ir/paper/331761/en

    Vancouver: Copy

    AGHBALI AMIRALA, MORADI ABBASABADI FARANAK, DELAZAR ABBAS, VOSOUGH HOSSEINI SEPIDEH, ZARE SHAHNEH FATEMEH, BARADARAN BEHZAD, JANANI MARYAM. INDUCTION OF APOPTOSIS AND CYTOTOXIC ACTIVITIES OF IRANIAN ORTHODOX BLACK TEA EXTRACT (BTE) USING IN VITRO MODELS. ADVANCED PHARMACEUTICAL BULLETIN[Internet]. 2014;4(3):255-260. Available from: https://sid.ir/paper/331761/en

    IEEE: Copy

    AMIRALA AGHBALI, FARANAK MORADI ABBASABADI, ABBAS DELAZAR, SEPIDEH VOSOUGH HOSSEINI, FATEMEH ZARE SHAHNEH, BEHZAD BARADARAN, and MARYAM JANANI, “INDUCTION OF APOPTOSIS AND CYTOTOXIC ACTIVITIES OF IRANIAN ORTHODOX BLACK TEA EXTRACT (BTE) USING IN VITRO MODELS,” ADVANCED PHARMACEUTICAL BULLETIN, vol. 4, no. 3, pp. 255–260, 2014, [Online]. Available: https://sid.ir/paper/331761/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