scholarly journals Effect of γ-oryzanol on Hepatic Cholesterol Biosynthesis and Fecal Excretion of Cholesterol Metablites

RADIOISOTOPES ◽  
1966 ◽  
Vol 15 (6) ◽  
pp. 371-374 ◽  
Author(s):  
Haruo NAKAMURA
2003 ◽  
Vol 73 (1) ◽  
pp. 39-47 ◽  
Author(s):  
A. Berger ◽  
G. Gremaud ◽  
M. Baumgartner ◽  
D. Rein ◽  
I. Monnard ◽  
...  

Amaranth was an important ancient grain and has current nutritional potential, being high in protein, fiber, lysine, magnesium, calcium, and squalene. Limited, inconsistent evidence demonstrates amaranth grain or oil can lower cholesterol in animal models. In the present study, hamsters received hypercholesterolemic diets consisting of a control, 10 or 20% Amaranthus cruentus grain, or 2.5 or 5% crude amaranth oil for four weeks. Amaranth oil (5%) decreased total and non-high-density lipoprotein (HDL) cholesterol by 15 and 22%, respectively, compared to control. Amaranth grain (20%; providing 1.4% amaranth oil) lowered non-HDL cholesterol and raised HDL cholesterol. Amaranth grain and oil decreased very low-density lipoprotein (VLDL) cholesterol by 21–50%; and increased fecal excretion of particular neutral sterols and the bile acid ursodeoxycholate. Amaranth oil (5%) additionally increased the cholesterol synthesis rate, possibly due to compensatory mechanisms; and decreased hepatic cholesterol ester, indicating reduced cholesterol ester availability for VLDL secretion and consistency with reduced VLDL cholesterol. Amaranth thus affected absorption of cholesterol and bile acids, cholesterol lipoprotein distribution, hepatic cholesterol content, and cholesterol biosynthesis. Amaranth grain and oil did not affect these pathways identically.


1966 ◽  
Vol 7 (5) ◽  
pp. 698-707
Author(s):  
R. Gordon Gould ◽  
E.A. Swyryd

1959 ◽  
Vol 196 (6) ◽  
pp. 1231-1237 ◽  
Author(s):  
R. Gordon Gould ◽  
Virginia L. Bell ◽  
Edith H. Lilly

Whole body x-irradiation resulted in an increased cholesterol biosynthesis in rat liver and adrenal glands, as measured by the rate of incorporation of either acetate-1-C14 or H3OH in intact animals. The effect was significant 24 hours postirradiation but was much larger at 48 hours, and was proportional to dosage over the range 300–2400 r. In liver the increase in rate was about 100%/100 r. Intestine showed no effect and carcass only a slight increase. Mice showed a small increase in hepatic cholesterol biosynthesis but rabbits and guinea pigs no significant change. Rats injected with both acetate-1-C14 and H3OH gave reasonably constant ratios of C14 and H3 in liver and carcass cholesterol in control and irradiated animals, supporting the hypothesis that the use of acetate-1-C14 in whole animals under standard conditions is a reliable measure of cholesterol biosynthetic rate. The proximate cause of the increased rate of cholesterol synthesis is postulated to be the decreased concentration; in liver a decrease of 0.12 mg/gm was correlated with a doubling of the synthetic rate.


1982 ◽  
Vol 65 (12) ◽  
pp. 2274-2280 ◽  
Author(s):  
Nancy L. Keim ◽  
Judith A. Marlett ◽  
Clyde H. Amundson ◽  
Linda D. Hagemann

Cell Research ◽  
2018 ◽  
Vol 29 (2) ◽  
pp. 151-166 ◽  
Author(s):  
Yanjing Guo ◽  
Meng Zhao ◽  
Tao Bo ◽  
Shizhan Ma ◽  
Zhongshang Yuan ◽  
...  

Steroids ◽  
1971 ◽  
Vol 17 (1-5) ◽  
pp. 541-557 ◽  
Author(s):  
Richard A. Jungmann ◽  
John S. Schweppe

1984 ◽  
Vol 4 (1) ◽  
pp. 137-144 ◽  
Author(s):  
Dana B. Ott ◽  
Paul A. Lachance

Author(s):  
Eva Gatineau ◽  
Gertrude Arthur ◽  
Audrey Poupeau ◽  
Kellea Nichols ◽  
Brett Spear ◽  
...  

Obesity is associated with alterations in hepatic lipid metabolism. We previously identified the prorenin receptor (PRR) as a potential contributor to liver steatosis. Therefore, we aimed to determine the relative contribution of PRR and its soluble form, sPRR, to lipid homeostasis. PRR-floxed male mice were treated with an adeno-associated virus with thyroxine-binding globulin promoter driven Cre to delete specifically PRR in hepatocytes (Liver PRR KO mice). Hepatic PRR deletion did not change the body weight but increased liver weights. Liver PRR KO mice exhibited higher plasma cholesterol levels and lower hepatic LDLR protein than control mice. Surprisingly, hepatic PRR deletion elevated hepatic cholesterol, and up-regulated hepatic SREBP2 and HMG CoA-R genes. In addition, the plasma levels of sPRR were significantly higher in Liver PRR KO mice compared with controls. In vitro studies in Hep-G2 cells demonstrated that sPRR treatment up-regulated SREBP2 suggesting that sPRR could contribute to hepatic cholesterol biosynthesis. Interestingly, PRR and total sPRR were elevated in the adipose tissue of Liver PRR KO mice suggesting that adipose tissue could contribute to the circulating pool of sPRR. Overall, this work supports previous works and open new area of investigation concerning the function of sPRR in lipid metabolism and adipose tissue - liver crosstalk.


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