語系:
繁體中文
English
說明(常見問題)
回圖書館首頁
手機版館藏查詢
登入
回首頁
切換:
標籤
|
MARC模式
|
ISBD
Effects of high sucrose diet on hepa...
~
Peters, Leandra Patricia.
FindBook
Google Book
Amazon
博客來
Effects of high sucrose diet on hepatic enzymes: Function and expression.
紀錄類型:
書目-語言資料,印刷品 : Monograph/item
正題名/作者:
Effects of high sucrose diet on hepatic enzymes: Function and expression./
作者:
Peters, Leandra Patricia.
面頁冊數:
116 p.
附註:
Chair: Robert W. Teel.
Contained By:
Dissertation Abstracts International63-08B.
標題:
Biology, Animal Physiology. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3063264
ISBN:
0493821244
Effects of high sucrose diet on hepatic enzymes: Function and expression.
Peters, Leandra Patricia.
Effects of high sucrose diet on hepatic enzymes: Function and expression.
- 116 p.
Chair: Robert W. Teel.
Thesis (Ph.D.)--Loma Linda University, 2002.
The physiological effects of dietary sucrose include hyperglycemia, and hepatic and peripheral insulin resistance. In this study Fisher 344 male weanling rats were fed a diet of either 65% sucrose (HSD) or standard lab chow (0% sucrose) for 90 days. We examined the effects of chronic HSD on hepatic enzymes, their quantity, function and activity.
ISBN: 0493821244Subjects--Topical Terms:
1017835
Biology, Animal Physiology.
Effects of high sucrose diet on hepatic enzymes: Function and expression.
LDR
:03460nam 2200337 a 45
001
929397
005
20110427
008
110427s2002 eng d
020
$a
0493821244
035
$a
(UnM)AAI3063264
035
$a
AAI3063264
040
$a
UnM
$c
UnM
100
1
$a
Peters, Leandra Patricia.
$3
1252882
245
1 0
$a
Effects of high sucrose diet on hepatic enzymes: Function and expression.
300
$a
116 p.
500
$a
Chair: Robert W. Teel.
500
$a
Source: Dissertation Abstracts International, Volume: 63-08, Section: B, page: 3538.
502
$a
Thesis (Ph.D.)--Loma Linda University, 2002.
520
$a
The physiological effects of dietary sucrose include hyperglycemia, and hepatic and peripheral insulin resistance. In this study Fisher 344 male weanling rats were fed a diet of either 65% sucrose (HSD) or standard lab chow (0% sucrose) for 90 days. We examined the effects of chronic HSD on hepatic enzymes, their quantity, function and activity.
520
$a
Growth and liver weight to body weight ratios, were significantly decreased in rats fed HSD compared to those fed 0% sucrose diet. Total hepatic microsomal cytochrome P450 (CYP450) content was unaltered by HSD. Cytochrome P450 1A1 and 3A2 isoforms were significantly decreased in quantity in the sucrose fed rats while CYP1A2, 2B1,2 isoforms were not. The percentage of the total P450 accounted for by CYP1A1,2, 2B1,2 and 3A2 was significantly decreased in rats maintained on the HSD.
520
$a
The activities of CYP1A1, 1A2 and 2B1,2 as determined by O-dealkylation of alkoxyresorufins were significantly decreased in the liver microsomes of HSD animals compared to those on standard lab chow. These decreases in activity of hepatic cytochromes suggest that HSD may also decrease the metabolism of xenobiotics that are substrates for these CYP450 isoforms. The activity of CYP3A2, was not significantly decreased in rats fed a HSD.
520
$a
CYP1A2 is implicated in the microsomal-dependent mutagenesis of heterocyclic amines (HCAs). Aflatoxin B<sub>1</sub> (AFB<sub>1</sub>) is a fungal toxin and food contaminant, and is implicated in human liver carcinogenesis. It is activated by CYP450 3A2, 1A2, and 2B1,2 isoforms. When liver microsomes were incubated with either of two HCAs (2-amino-3,8-dimethyl-imidazo[4,5-<italic> f</italic>]quinoxaline (MeIQx) and 2-amino-3-methyl-imidazo[4,5-<italic>f </italic>]quinoline (IQ), there was a significant decrease in mutagenesis evidenced by the number of His<super>+</super> revertants in <italic>Salmonella typhymurium</italic> TA98. There was a statistically significant increase in the number of <italic>S. typhimurium</italic> His<super>+</super> revertants induced by AFB<sub>1</sub> in the presence of hepatic microsomes from rats fed a HSD.
520
$a
Glutathione-S-transferase (GST) enzymatic activity is essential for the elimination of products of the metabolism of xenobiotics and is found in the cytosol conjugating glutathione to other moieties rendering them more hydrophilic and excretable. In the sucrose fed rats the activity of GSTs was significantly decreased, suggesting that a HSD may alter the elimination of metabolites.
590
$a
School code: 0106.
650
4
$a
Biology, Animal Physiology.
$3
1017835
650
4
$a
Health Sciences, Nutrition.
$3
1017801
650
4
$a
Health Sciences, Pharmacology.
$3
1017717
690
$a
0419
690
$a
0433
690
$a
0570
710
2 0
$a
Loma Linda University.
$3
1020166
773
0
$t
Dissertation Abstracts International
$g
63-08B.
790
$a
0106
790
1 0
$a
Teel, Robert W.,
$e
advisor
791
$a
Ph.D.
792
$a
2002
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3063264
筆 0 讀者評論
館藏地:
全部
電子資源
出版年:
卷號:
館藏
1 筆 • 頁數 1 •
1
條碼號
典藏地名稱
館藏流通類別
資料類型
索書號
使用類型
借閱狀態
預約狀態
備註欄
附件
W9100701
電子資源
11.線上閱覽_V
電子書
EB W9100701
一般使用(Normal)
在架
0
1 筆 • 頁數 1 •
1
多媒體
評論
新增評論
分享你的心得
Export
取書館
處理中
...
變更密碼
登入