• ايلاف محمود شهاب
  • Elaf Mahmoud Shehab
  • تدريسي : كلية الصيدلة
  • Teaching : college of Pharmacy
  • ماجستير علم الادوية والسموم
  • msc pharmacology and toxicoloy
  • elaf.mahmood@esraa.edu.iq
  • phelafmahmood86@yahoo.com
  • نشاطات التدريسي

    نشاطات التدريسي

    المقررات المكلف بها

    المقررات المكلف بها

    المقررات المكلف بها - 7
    القسم المرحلة الفصل رمز المقرر الوحدات توصيف المقرر
    كلية الصيدلة المرحلة الثالثة فصل ثاني PHR0931 3 Pharmacology I
    كلية الصيدلة المرحلة الرابعة فصل اول PHR0942 4 Pharmacology II
    كلية الصيدلة المرحلة الرابعة فصل ثاني IPH0941 4 Industrial pharmacy I laboratory
    كلية الصيدلة المرحلة الرابعة فصل ثاني PHR0943 2 Pharmacology III
    كلية الصيدلة المرحلة الخامسة فصل اول 2 Clinical toxicology laboratory
    كلية الصيدلة المرحلة الرابعة فصل اول 2 Pharmacology II laboratory
    كلية الصيدلة المرحلة الرابعة فصل ثاني 2 General toxicology laboratory
    المحاضرات الالكترونية

    المحاضرات الالكترونية

    المحاضرات الالكترونية - 18
    العام المقرر القسم المرحلة المحاضرة
    2022-2023 Pharmacology II كلية الصيدلة المرحلة الرابعة drugs for heart failure
    2022-2023 General toxicology laboratory كلية الصيدلة المرحلة الرابعة Gastrointestinal and antiemetic drugs
    2022-2023 Pharmacology II كلية الصيدلة المرحلة الرابعة Drugs for Hyperlipidemia
    2022-2023 General toxicology laboratory كلية الصيدلة المرحلة الرابعة ANTICOAGULANTS AND ANTIPLATELET AGENTS
    2022-2023 Pharmacology II كلية الصيدلة المرحلة الرابعة drugs for disorders of respiratory system
    2022-2023 General toxicology laboratory كلية الصيدلة المرحلة الرابعة antidepressants
    2022-2023 Pharmacology II كلية الصيدلة المرحلة الرابعة anxiolytic drugs
    2022-2023 General toxicology laboratory كلية الصيدلة المرحلة الرابعة Drugs for Neurodegenerative Diseases
    2022-2023 Pharmacology II كلية الصيدلة المرحلة الرابعة introduction to central nervous system
    2022-2023 Pharmacology II laboratory كلية الصيدلة المرحلة الرابعة DRUGS AND HUMAN EYES
    2022-2023 Pharmacology II laboratory كلية الصيدلة المرحلة الرابعة Barbiturates
    2022-2023 Pharmacology II laboratory كلية الصيدلة المرحلة الرابعة Routes of administrations
    2022-2023 Pharmacology II كلية الصيدلة المرحلة الرابعة anticancer drugs I
    2022-2023 Pharmacology II كلية الصيدلة المرحلة الرابعة estrogens and androgens
    2022-2023 Pharmacology II كلية الصيدلة المرحلة الرابعة Pituitary and Thyroid
    2022-2023 Pharmacology II كلية الصيدلة المرحلة الرابعة osteoporosis
    2022-2023 Pharmacology II كلية الصيدلة المرحلة الرابعة nonsteroidal antiinflamatory drugs part II
    2022-2023 Pharmacology II كلية الصيدلة المرحلة الرابعة nonsteroidal antiinflamatory drugs part I
    البحوث

    البحوث

    2018 Journal of Global Pharma Technology

    2021 Annals of the Romanian Society for Cell Biology
    Autophagy is an adaptive evolutionary machine induced in all eukaryotic cells under different forms of cellular stimuli such as stress, amino acid, starvation and excessive loss in trophic factors and hormones to removes damaged organelles and proteins from cells andkeep the cellular homeostasis. Since various diseases including cancer formed in response to dysregulation of autophagy, wide attention has been developed for understanding the ambiguous roles of autophagy in tumor suppression. Protein kinase A (PKA), 5’-AMP-activated protein kinase (AMPK) and mTOR complex 1 (mTORC1) are the main kinases that regulate this process. Targeting these kinases and other autophagy regulatory genes have been revealed an excellent result in the treatment of many resistance cancer cells such as breast and prostate cancer. This review will focus on the molecular mechanism, the main genes involved in the regulation of each step of autophagy, and how these genes have been targeted as a novel step in cancer therapy.IntroductionAutophagy can be defined as a preserved catabolic machine that is participating in homeostasis in cells which was required to keep the normal cellular physiology under stressed circumstances[1]. Autophagic cell death (ACD) occurs as an adaptive process in all eukaryotic cells as a response to various forms of stimuli including stress, amino acid starvation, excessive falls in trophic factors and hormones [2], lipid malnourishment, and diminished intracellular cholesterol tracking[3]. All these stimuli can induce the function of autophagy and guide to diverse morphological consequences via different signaling pathways. Tumor cells can gain resistance to apoptosis via expressing anti-apoptotic proteins like B-cell lymphoma 2 (BCL-2) or by downregulating pro-apoptotic proteins. Defect in apoptosis has induced cancer and contribute in resistance to chemotherapy, this lead to alteration to
     
    Autophagy is an adaptive evolutionary machine induced in all eukaryotic cells under different forms of cellular stimuli such as stress, amino acid, starvation and excessive loss in trophic factors and hormones to removes damaged organelles and proteins from cells andkeep the cellular homeostasis. Since various diseases including cancer formed in response to dysregulation of autophagy, wide attention has been developed for understanding the ambiguous roles of autophagy in tumor suppression. Protein kinase A (PKA), 5’-AMP-activated protein kinase (AMPK) and mTOR complex 1 (mTORC1) are the main kinases that regulate this process. Targeting these kinases and other autophagy regulatory genes have been revealed an excellent result in the treatment of many resistance cancer cells such as breast and prostate cancer. This review will focus on the molecular mechanism, the main genes involved in the regulation of each step of autophagy, and how these genes have been targeted as a novel step in cancer therapy.IntroductionAutophagy can be defined as a preserved catabolic machine that is participating in homeostasis in cells which was required to keep the normal cellular physiology under stressed circumstances[1]. Autophagic cell death (ACD) occurs as an adaptive process in all eukaryotic cells as a response to various forms of stimuli including stress, amino acid starvation, excessive falls in trophic factors and hormones [2], lipid malnourishment, and diminished intracellular cholesterol tracking[3]. All these stimuli can induce the function of autophagy and guide to diverse morphological consequences via different signaling pathways. Tumor cells can gain resistance to apoptosis via expressing anti-apoptotic proteins like B-cell lymphoma 2 (BCL-2) or by downregulating pro-apoptotic proteins. Defect in apoptosis has induced cancer and contribute in resistance to chemotherapy, this lead to alteration to
     
     

    2021 International Journal of Pharmaceutical Research

    2020 International Journal of Pharmaceutical Research

    2021 Turkish Journal of Physiotherapy and Rehabilitation

    Background: Total knee arthroplasty is a successful procedure for relieving pain and restoring function in cases with severe rheumatoid arthritis and osteoarthritis. Local infiltration analgesia is becoming more commonly used owing to the excellent pain relief, the low frequency of complications, and the antiinflammatory effect. Aim of study: To evaluate the efficacy of local infiltrative analgesia when it’s use in total knee arthroplasty patients for decrease the pain score and increase range of motion in early post-operative rehabilitation. Methods: During the period from October 2016 to September 2018, a comparative prospective study was applied for 36 patients in Medical City, Hospital of Specialized Surgeries and Private Nursing Home Hospital. All patients were indicated for primary total knee arthroplasty which is done by the same surgical team and then followed-up to November 2018. They were divided into two groups, Group A included 16 patients managed with local infiltrative analgesia, while group B included 20 patients managed without local infiltrative analgesia. Patients with a history of deep venous thrombosis or pulmonary embolism or on longterm warfarin therapy, undergoing revision procedure, with a history of allergy or intolerance to 1 of the study drugs, with rheumatoid arthritis, and abnormal liver enzymes were excluded from this study. Assessment of clinical function was based on the range of motion score, straight leg raise pre and postoperatively, and VAS score scale postoperatively during rest and during movement.  Results: In group A, means of ROM score one day and two days postoperatively were decreased than that before operation (105.12 versus 89.37, P= 0.001 and 105.12 versus 87.37, P= 0.001 respectively). In group B, means of this score one day and two days postoperatively were decreased than that before operation (105.75 versus 88.50, P=0.001 and 105.75 versus 82.75, P= 0.001 respectively). During rest, means of VAS score four hours, 12 hours, one day, and two days after operation were significantly decreased in patients managed with LIA (group A) compared to means of patients in group B. (2.70 versus 1.87, P= 0.016; 3.45 versus 2.25, P=0.003; 3.90 versus 3.12, P=0.026; and 4.50 versus 3.50, P=0.002 respectively). During movement, statistically insignificant differences in means of VAS score between study groups four hours, 12 hours, and two days after operation (P= 0.258, 0.057, and 0.284 respectively). While mean of this score one day postoperatively was decreased in patients of group A compared to that in patients of group B and this difference in means was statistically significant (P=0.016).  Conclusion: Local infiltration analgesia effectively reduces pain scores during rest and movement also reduces hospital stay in patients undergoing total knee arthroplasty, and better physiotherapy outcome. 

    2017 International Journal of Pharmaceutical Sciences Review and Research
    المؤلفات

    المؤلفات

    2023 العراق