The role of Cydonia oblonga, Portulaca oleracea, and Artemisia dracunculus on hypoxia

سال انتشار: 1402
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 69

فایل این مقاله در 7 صفحه با فرمت PDF قابل دریافت می باشد

استخراج به نرم افزارهای پژوهشی:

لینک ثابت به این مقاله:

شناسه ملی سند علمی:

JR_JKMU-30-4_008

تاریخ نمایه سازی: 3 مهر 1402

چکیده مقاله:

Background:Hypoxia exists in some malignancies and is a prognostic risk factor contributing to tumor growth and metastasis. Anti-hypoxic compounds may improve this situation and be considered anti-cancer agents. In previous reports, Cydonia oblonga, Portulaca oleracea, and Artemisia dracunculus showed anti-cancer activity. So, we investigated the anti-hypoxic activities of C. oblonga, P. oleracea, and A. dracunculus to evaluate the possible mechanism of the plant's effectiveness in treating cancer.Methods:Total phenolic and flavonoid contents and HPLC analysis were performed on C. oblonga leaves, P. oleracea, and A. dracunculus aerial parts extract. Anti-hypoxic activities were evaluated in asphyctic, haemic, and circulatory hypoxia models.Results:A. dracunculus extract (at ۲۵۰ mg/kg) significantly improved the survival time compared to the normal saline (P < ۰.۰۰۰۱) in asphyctic hypoxia, even its effect was significantly better than phenytoin in this dose (P = ۰.۰۰۰۵). Although the extracts increased the survival time in other doses, their effects were not significant (P > ۰.۰۵). In haemic hypoxia, the extracts were ineffective at any dose (P > ۰.۰۵). At ۲۵۰ mg/kg, P. oleracea and A. dracunculus significantly increased the survival time (P < ۰.۰۰۱ and P < ۰.۰۵, respectively) in circulatory hypoxia. Their effects were similar to propranolol (P > ۰.۰۵).Conclusions:The anti-cancer effects of C. oblonga are not dependent on the anti-hypoxic effects. P. oleracea and A. dracunculus have anti-hypoxic effects only in high doses, indicating their extracts' weak anti-hypoxic ability or the presence of potent anti-hypoxic compounds with low concentrations in them.

کلیدواژه ها:

نویسندگان

Mohammad Hossein Hosseinzadeh

Pharmaceutical Sciences Research Center, Hemoglobinopathy Institute, Mazandaran University of Medical Sciences, Sari, Iran.

Mohammad Eghbali

Pharmaceutical Sciences Research Center, Hemoglobinopathy Institute, Mazandaran University of Medical Sciences, Sari, Iran.

Zahra Hashemi

Department of Medicinal Chemistry, Faculty of Pharmacy, Ayatollah Amoli Branch, Islamic Azad University, Amol, Iran.

Narges Naserirad

Ramsar International Campus, Pardis School of Pharmacy, Mazandaran University of Medical Sciences, Ramsar, Iran.

Mahbube Shirdel

Ramsar International Campus, Pardis School of Pharmacy, Mazandaran University of Medical Sciences, Ramsar, Iran.

Melika Rafizadeh

Ramsar International Campus, Pardis School of Pharmacy, Mazandaran University of Medical Sciences, Ramsar, Iran.

Davood Farzin

Pharmaceutical Sciences Research Center, Hemoglobinopathy Institute, Mazandaran University of Medical Sciences, Sari, Iran.

Mohammad Ali Ebrahimzadeh

Pharmaceutical Sciences Research Center, Hemoglobinopathy Institute, Mazandaran University of Medical Sciences, Sari, Iran.