Lewis D S, Oren S, Wang X, Moyer M L, Beitz D C, Knight T J, Mott G E
Department of Food Science and Human Nutrition, Iowa State University, Ames 50011, USA.
J Anim Sci. 2000 Apr;78(4):943-51. doi: 10.2527/2000.784943x.
Hepatic cholesterol 7alpha-hydroxylase (CYP7A) and sterol 27 hydroxylase activities were measured in fetal, newborn, suckling, and weaned piglets from 76 d into gestation to 49 d of age. Hepatic CYP7A activity was not detected in fetal microsomes, but it increased to 6.8 +/- 2.6 pmol/min x mg(-1) protein in suckling piglets at 21 d of age and to 18.2 +/- 2.5 in weaned piglets at 49 d of age. Hepatic CYP7A activity was not different between 49-d-old piglets weaned at 21 d and piglets suckled for 49 d (18.9 +/- 2.6 and 18.2 +/- 2.5 pmol/min x mg protein, respectively). Fasting for 14 h decreased CYP7A activity by 86% in both suckled and weaned piglets. Cholesterol 7alpha-hydroxylase activity remained decreased for at least 5 h after refeeding. Sterol 27-hydroxylase activity was also undetectable near birth, but was detectable by 21 d of age. Postnatally, sterol 27-hydroxylase activity was not influenced by age or suckling and weaning, as was CYP7A. Sterol 27-hydroxylase was decreased by 80% in piglets deprived of feed compared with piglets given free access. In contrast to CYP7A activity, 27-hydroxylase activity returned within 5 h after refeeding to levels observed in piglets given ad libitum access to feed. Similar to CYP7A enzyme activity, hepatic CYP7A mRNA was not detected in newborn piglets, but increased from 2.7 +/- 1.7 pg mRNA/microg RNA in suckling piglets at 21 d to 13.7 +/- 1.2 in 49-d-old piglets weaned at 21 d. As with enzyme activity, feed deprivation decreased CYP7A mRNA to barely detectable levels (< .5 pg/microg RNA), and which remained decreased for at least 5 h following refeeding (.6 +/- .3 and 2.67 +/- .4 pg mRNA/microg RNA for suckled and weaned piglets, respectively). In piglets allowed free access to feed, CYP7A mRNA concentrations were associated positively (P = .001) with enzyme activity. These results suggest that developmental regulation of CYP7A activity is the result of a pretranslational mechanism.
在妊娠76天至49日龄的胎儿、新生仔猪、哺乳仔猪和断奶仔猪中,测定了肝脏胆固醇7α-羟化酶(CYP7A)和甾醇27-羟化酶的活性。在胎儿微粒体中未检测到肝脏CYP7A活性,但在21日龄的哺乳仔猪中增加到6.8±2.6 pmol/分钟×毫克(-1)蛋白质,在49日龄的断奶仔猪中增加到18.2±2.5。在21日龄断奶的49日龄仔猪和哺乳49天的仔猪之间,肝脏CYP7A活性没有差异(分别为18.9±2.6和18.2±2.5 pmol/分钟×毫克蛋白质)。禁食14小时使哺乳仔猪和断奶仔猪的CYP7A活性均降低86%。再喂食后,胆固醇7α-羟化酶活性至少5小时仍保持降低。甾醇27-羟化酶活性在出生时也未检测到,但在21日龄时可检测到。出生后,甾醇27-羟化酶活性不受年龄、哺乳和断奶的影响,CYP7A也是如此。与自由采食的仔猪相比,禁食仔猪的甾醇27-羟化酶降低了80%。与CYP7A活性相反,再喂食后5小时内,27-羟化酶活性恢复到自由采食仔猪中观察到的水平。与CYP7A酶活性相似,新生仔猪肝脏中未检测到CYP7A mRNA,但在21日龄的哺乳仔猪中从2.7±1.7 pg mRNA/微克RNA增加到21日龄断奶的49日龄仔猪中的13.7±1.2。与酶活性一样,饲料剥夺使CYP7A mRNA降低到几乎检测不到的水平(<0.5 pg/微克RNA),再喂食后至少5小时仍保持降低(哺乳仔猪和断奶仔猪分别为0.6±0.3和2.67±0.4 pg mRNA/微克RNA)。在自由采食的仔猪中,CYP7A mRNA浓度与酶活性呈正相关(P = 0.001)。这些结果表明,CYP7A活性的发育调节是翻译前机制的结果。