بررسی اثر کورکومین بر محافظت عصبی در مدل سلولی بیماری پارکینسون القاء شده با سم 6– هیدروکسی دوپامین
محورهای موضوعی : فصلنامه زیست شناسی جانوری
مهدیه آذرشب
1
(گروه زیست شناسی، واحد تهران شمال، دانشگاه آزاد اسلامی، تهران، ایران)
رامین حاجی خانی
2
(گروه زیست شناسی، واحد تهران شمال، دانشگاه آزاد اسلامی، تهران، ایران)
مهدی رهنما
3
(گروه زیست شناسی، واحد زنجان، دانشگاه آزاد اسلامی، زنجان، ایران)
محمدرضا بیگدلی
4
(گروه زیست شناسی، دانشکده علوم زیستی، دانشگاه شهید بهشتی، تهران، ایران)
جلال صولتی
5
(گروه زیست شناسی، واحد کرج، دانشگاه آزاد اسلامی، کرج، ایران)
کلید واژه: کورکومین, پارکینسون, سلول کاتکول آمینرژیک, 6– هیدروکسی دوپامین,
چکیده مقاله :
بیماری پارکینسون یکی از شایع ترین انواع بیماری های نورودژنراتیو است که با اختلالات حرکتی مانند کندی حرکت، فقدان حرکت، سختی عضلانی و لرزش در حال استراحت و کاهش قدرت صدا مشخص می شود. علت اصلی بیماری، تخریب نورون های دوپامینرژیک بخش متراکم جسم سیاه در مغز میانی و کاهش غلظت دوپامین در پایانه های جسم مخطط است. این مطالعه، به منظور بررسی اثر کورکومین بر مدل سلولی بیماری پارکینسون القاء شده با سم 6-هیدروکسی دوپامین با هدف کاهش التهاب سلولی انجام شد. محیط کشت مورد استفاده در این مطالعهFBS+DMEM 10 درصد برای مطالعه سلول های کاتکول آمینرژیک می باشد. برای ایجاد مدل سلولی پارکینسون از سم 6- هیدروکسی دوپامین استفاده شد. از دوزهای20، 25 و 30 میلی گرم بر کیلوگرم کورکومین به عنوان دارو و برای شمارش سلول های زنده از دو روش رنگ آمیزیMTT و BT استفاده شد. نتایج مطالعه حاضر، نشان دادکه مصرف کورکومین می تواند منجربه افزایش توان آنتی اکسیدانتی وحافظت سلول از آسیب های ناشی از بنیان های فعال اکسیژن گردد. درمان باکورکومین به جهت خاصیت ضدالتهابی، با توجه به نتایج آزمون MTT و BT نیز نشان داد که حفاظت سلولی افزایش، مرگ سلول های کاتکول آمینرژیک توسط سم 6 – هیدروکسی دوپامین به صورت معناداری کاهش یافته است. که نشان دهنده اثرات آنتی اکسیدانتی و ضدالتهابی کورکومین، در برابر آسیب های ناشی از بیماری پارکینسون و کاهش پیشرفت علایم بیماری می باشد.
Parkinson's disease is one of the most common types of the neurodegenerative disease, which is characterized by the movement disorders such as slowness, lack of movement, muscle stiffness, and resting tremor, and hypophonic. The main reason of disease is the destruction of dopaminergic neurons in the Substantia Nigra in the midbrain and a decrease in dopamine concentration in the striatum terminals. In this study, used culture medium was DMEM with FBS, and the cells under study were catecholaminergic cells.6-Hydroxy dopamine toxin was used on cells to create a Parkinson cell model. Curcumin was used as a drug, and MTT, and BT methods were used to count the living cells. This research was designed to study the curcumin effect on Parkinson's disease with cellular model induced by 6-Hydroxy dopamine toxin with reduced inflammation. This study's results showed that using curcumin can increase the antioxidant power and protect the cell from damage caused by reactive oxygen species. Due to the results of MTT, and curcumin treatment due to its anti-inflammatory properties BT test also showed that cellular protection had increased, the death of aminergic catechol cells by 6-hydroxy dopamine toxin was significantly reduced. It shows the antioxidant and anti-inflammatory effects of curcumin on the damage caused by Parkinson's disease and reducing the progression of symptoms. Treatment withcurcumin to be anti-inflammatory can reduce the death of catecholaminergic cells by 6-hydroxy dopamine toxin.
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