کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5559519 1403288 2016 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Developmental expression of paraoxonase 2
ترجمه فارسی عنوان
بیان رشد پاراکسوناز 2
کلمات کلیدی
پاراکسوناز 2، توسعه، مغز، کبد، استرس اکسیداتیو، پاراکسوناز 1، پاراکسوناز 3،
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست بهداشت، سم شناسی و جهش زایی
چکیده انگلیسی


- Paraoxonase 2 (PON2) is differentially expressed in brain of male and female mice and non-human primates.
- PON2 protein and mRNA increase then decrease during development in brain from mice and non-human primates.
- PON2 protein and mRNA, similarly to PON1 and PON3, increase with age in mice.

Paraoxonase 2 (PON2) is a member of the paraoxonase gene family also comprising PON1 and PON3. PON2 functions as a lactonase and exhibits anti-bacterial as well as antioxidant properties. At the cellular level, PON2 localizes to the mitochondrial and endoplasmic reticulum membranes where it scavenges reactive oxygen species. PON2 is of particular interest as it is the only paraoxonase expressed in brain tissue and appears to play a critical role in mitigating oxidative stress in the brain. The aim of this study was to investigate the expression of PON2 at the protein and mRNA level in the brain and liver of mice through development to identify potential age windows of susceptibility to oxidative stress, as well as to compare expression of hepatic PON2 to expression of PON1 and PON3. Overall, PON2 expression in the brain was lower in neonatal mice and increased with age up to postnatal day (PND) 21, with a significant decrease observed at PND 30 and 60. In contrast, the liver showed continuously increasing levels of PON2 with age, similar to the patterns of PON1 and PON3. PON2 protein levels were also investigated in brain samples from non-human primates, with PON2 increasing with age up to the infant stage and decreasing at the juvenile stage, mirroring the results observed in the mouse brain. These variable expression levels of PON2 suggest that neonatal and young adult animals may be more susceptible to neurological insult by oxidants due to lower levels of PON2 in the brain.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Chemico-Biological Interactions - Volume 259, Part B, 25 November 2016, Pages 168-174
نویسندگان
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