![The Impact of beta, beta-Carotene - 9',10'- Oxygenase2 (BCO2) on Mitochondrial Function and Hypothalamic Metabolism için kapak resmi The Impact of beta, beta-Carotene - 9',10'- Oxygenase2 (BCO2) on Mitochondrial Function and Hypothalamic Metabolism için kapak resmi](/client/assets/d79c3e4af2b6d196/ctx/images/no_image.png)
The Impact of beta, beta-Carotene - 9',10'- Oxygenase2 (BCO2) on Mitochondrial Function and Hypothalamic Metabolism
Başlık:
The Impact of beta, beta-Carotene - 9',10'- Oxygenase2 (BCO2) on Mitochondrial Function and Hypothalamic Metabolism
Yazar:
Guo, Xin, author.
ISBN:
9780438076013
Yazar Ek Girişi:
Fiziksel Tanımlama:
1 electronic resource (89 pages)
Genel Not:
Source: Masters Abstracts International, Volume: 57-06M(E).
Advisors: Dingbo Lin Committee members: Winyoo Chowanadisai; Stephen Clarke; Edralin Lucas.
Özet:
beta,beta-carotene-9',10'-oxygenase2 (BCO2) is a carotenoid cleavage enzyme localized to the inner membrane of mitochondria. Hypothalamus is the key brain region that regulates energy homeostasis through nutrient sensing and signal integration from central and peripheral pathways. The aim of this study is to explore the impact of BCO2 on maintaining mitochondrial function and hypothalamic metabolism, as well as the mechanism of why BCO2 -/- mice exhibit orexigenic phenotype. Using 129S6 wild type (WT) and BCO2 -/- mice model, we measured metabolic profiling differences in hypothalamus caused by the deletion of the BCO2 gene. Mitochondrial proteomic and functional analyses were also conducted to evaluate the impact of BCO2 on mitochondria. Metabolomics results revealed striking metabolic changes between genotypes. The top ranking metabolites in distinguishing WT and BCO2 -/- mice suggested key differences in transport of long chain fatty acids into mitochondria, biosynthesis of bile acids; metabolism of sulfur-containing amino acids; and markers of inflammation. The significantly lower long chain fatty acids and glucose in the hypothalamus may regulate energy homeostasis by altering nutrient sensing. Within the mitochondria, altered pathways including the proteins involved in Krebs cycle, electron transport chain and fatty acids beta-oxidation were observed in hypothalamic mitochondria of BCO2 -/- mice. The deletion of BCO2 also led to the significantly decreased capacity of complex II of electron transport chain. In conclusion, the absence of BCO2 may be closely associated with hypothalamic metabolism disorder and mitochondrial dysfunction caused by the perturbed energy utilization. The significantly lower leptin level and lower hypothalamic glucose and lipids sensing may be the major contributor to the enhanced appetite in BCO2-/- mice.
Notlar:
School code: 0664
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Yer Numarası | Demirbaş Numarası | Shelf Location | Lokasyon / Statüsü / İade Tarihi |
---|---|---|---|
XX(687593.1) | 687593-1001 | Proquest E-Tez Koleksiyonu | Arıyor... |
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