Early oleate deficiency leads to severe defects in fetal rat liver development

Early oleate deficiency leads to severe defects in fetal rat liver development


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نویسندگان: فاطمه محمدزاده , علیرضا علی همتی , عباس پیرپور تازه کند , مسعود دارابی امین , امیر مهدی زاده حقیقی

کلمات کلیدی: Development Embryo Hepatocytes Monounsaturated fatty acids Pregnancy

نشریه: 16525 , 9 , 22 , 2019

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نویسنده ثبت کننده مقاله مسعود دارابی امین
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه بیماری های گوارش و کبد
کد مقاله 68240
عنوان فارسی مقاله Early oleate deficiency leads to severe defects in fetal rat liver development
عنوان لاتین مقاله Early oleate deficiency leads to severe defects in fetal rat liver development
ناشر 5
آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ بلی
عنوان نشریه (خارج از لیست فوق)
نوع مقاله Original Article
نحوه ایندکس شدن مقاله ایندکس شده سطح یک – ISI - Web of Science
آدرس لینک مقاله/ همایش در شبکه اینترنت

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Objective(s): Oleate can be produced through de novo synthesis, which contributes to biological processes and signaling pathways. However, the role of this non-essential fatty acid in hepatic development remains unclear. The current study aimed to evaluate the influence of early oleate deficiency induced by the inhibitor of de novo oleate synthesis MF-438 on fetal rat liver development. Materials and Methods: Female Wistar rats with an average weight of 200±20 g were subjected to this study. After mating, pregnant rats were divided into three groups and gavaged with the vehicle, MF 438 or MF-438 plus oleate from day 3 of pregnancy for five days. Obtained fetuses were sacrificed and the liver tissues were retrieved. Hepatic morphological index, biochemical markers, and gene expression of hepatic development markers were analyzed using Hematoxylin-Eosine, spectrometry, and real-time PCR techniques, respectively. Results: Relatively, deficient morphological indices and hepatic maturation markers were observed in fetus livers of the inhibitor-treated group. In comparison to the other two groups, total hepatic protein and glycogen content were increased with treatment of MF-438 plus oleate. Hepatocyte nuclear factor 1α, alpha fetoprotein, albumin, and cytochrome P450 gene expression were also significantly increased in the group treated with both MF-438 and oleate. Conclusion: Our data indicate that oleate availability during early embryo development is linked with fetal rat liver development.

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نویسنده نفر چندم مقاله
فاطمه محمدزادهاول
علیرضا علی همتیدوم
عباس پیرپور تازه کندسوم
مسعود دارابی امینچهارم
امیر مهدی زاده حقیقیپنجم

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2019 IJBMS Early oleate deficiency leads.pdf1398/05/13601685دانلود