کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5508369 | 1537687 | 2017 | 56 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Phytol-induced pathology in 2-hydroxyacyl-CoA lyase (HACL1) deficient mice. Evidence for a second non-HACL1-related lyase
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کلمات کلیدی
SCPxTPPPBDMEFMFPORODEXAARDPPARPTSα-Oxidation - α-اکسیداسیونω-Oxidation - ω اکسیداسیونperoxisome biogenesis disorder - اختلال بیوژنز پراکسسیومPhytanic acid - اسید فیتانیکWAT, White adipose tissue - بافت چربی سفید، بافت ادیپوز سفیدThiamine pyrophosphate - تیامین پری فسفاتThiamine - تیامین، ویتامین B1dual energy X-ray absorptiometry - جذب سنجی اشعه ایکس انرژی دوگانهCNS - دستگاه عصبی مرکزیOil red O - روغن قرمز Ocentral nervous system - سیستم عصبی مرکزیperoxisome targeting signal - سیگنال هدف قرار دادن پراکسیومendoplasmic reticulum - شبکه آندوپلاسمی Mass spectrometry - طیف سنجی جرمیMouse model - مدل موشmouse embryonic fibroblasts - موش فیبروبلاست جنینیknockout - ناکاوتPeroxisomes - پراکسیوم هاMultifunctional protein - پروتئین چند منظورهWAT - چیliquid chromatography - کروماتوگرافی مایعGas chromatography - کروماتوگرافی گازیPeroxisome proliferator activated receptor - گیرنده فعال فعال پروکسیوم
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
زیست شیمی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
2-Hydroxyacyl-CoA lyase (HACL1) is a key enzyme of the peroxisomal α-oxidation of phytanic acid. To better understand its role in health and disease, a mouse model lacking HACL1 was investigated. Under normal conditions, these mice did not display a particular phenotype. However, upon dietary administration of phytol, phytanic acid accumulated in tissues, mainly in liver and serum of KO mice. As a consequence of phytanic acid (or a metabolite) toxicity, KO mice displayed a significant weight loss, absence of abdominal white adipose tissue, enlarged and mottled liver and reduced hepatic glycogen and triglycerides. In addition, hepatic PPARα was activated. The central nervous system of the phytol-treated mice was apparently not affected. In addition, 2OH-FA did not accumulate in the central nervous system of HACL1 deficient mice, likely due to the presence in the endoplasmic reticulum of an alternate HACL1-unrelated lyase. The latter may serve as a backup system in certain tissues and account for the formation of pristanic acid in the phytol-fed KO mice. As the degradation of pristanic acid is also impaired, both phytanoyl- and pristanoyl-CoA levels are increased in liver, and the Ï-oxidized metabolites are excreted in urine. In conclusion, HACL1 deficiency is not associated with a severe phenotype, but in combination with phytanic acid intake, the normal situation in man, it might present with phytanic acid elevation and resemble a Refsum like disorder.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids - Volume 1862, Issue 9, September 2017, Pages 972-990
Journal: Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids - Volume 1862, Issue 9, September 2017, Pages 972-990
نویسندگان
Serena Mezzar, Evelyn De Schryver, Stanny Asselberghs, Els Meyhi, Petruta L. Morvay, Myriam Baes, Paul P. Van Veldhoven,