RESUMO
Prostate cancer cells derived from transgenic mice with adenocarcinoma of the prostate (TRAMP cells) were treated with the HMG-CoA reductase inhibitor, lovastatin. This caused inactivation of the small GTPase RhoA, actin stress fiber disassembly, cell rounding, growth arrest in the G1 phase of the cell cycle, cell detachment and apoptosis. Addition of geranylgeraniol (GGOL) in the presence of lovastatin, to stimulate protein geranylgeranylation, prevented lovastatin's effects. That is, RhoA was activated, actin stress fibers were assembled, the cells assumed a flat morphology and cell growth resumed. The following observations support an essential role for RhoA in TRAMP cell growth: (1) TRAMP cells expressing dominant-negative RhoA (T19N) mutant protein displayed few actin stress fibers and grew at a slower rate than controls (35 h doubling time for cells expressing RhoA (T19N) vs 20 h for untransfected cells); (2) TRAMP cells expressing constitutively active RhoA (Q63L) mutant protein displayed a contractile phenotype and grew faster than controls (13 h doubling time). Interestingly, addition of farnesol (FOL) with lovastatin, to stimulate protein farnesylation, prevented lovastatin-induced cell rounding, cell detachment and apoptosis, and stimulated cell spreading to a spindle shaped morphology. However, RhoA remained inactive and growth arrest persisted. The morphological effects of FOL addition were prevented in TRAMP cells expressing dominant-negative H-Ras (T17N) mutant protein. Thus, it appears that H-Ras is capable of inducing cell spreading, but incapable of supporting cell proliferation, in the absence of geranylgeranylated proteins like RhoA.
Assuntos
Adenocarcinoma/patologia , Alquil e Aril Transferases/fisiologia , Antineoplásicos/farmacologia , Proteínas de Ligação ao GTP/fisiologia , Inibidores de Hidroximetilglutaril-CoA Redutases/farmacologia , Lovastatina/farmacologia , Neoplasias da Próstata/patologia , Processamento de Proteína Pós-Traducional/efeitos dos fármacos , Citoesqueleto de Actina/efeitos dos fármacos , Citoesqueleto de Actina/metabolismo , Adenocarcinoma/genética , Adenocarcinoma/metabolismo , Alquil e Aril Transferases/genética , Animais , Apoptose , Adesão Celular , Divisão Celular/efeitos dos fármacos , Tamanho Celular , Diterpenos/farmacologia , Interações Medicamentosas , Ativação Enzimática , Farneseno Álcool/farmacologia , Fase G1 , Proteínas de Ligação ao GTP/genética , Proteínas de Ligação ao GTP/metabolismo , Genes ras , Guanosina Trifosfato/fisiologia , Masculino , Ácido Mevalônico/metabolismo , Camundongos , Camundongos Transgênicos , Fosfatos de Poli-Isoprenil/metabolismo , Neoplasias da Próstata/genética , Neoplasias da Próstata/metabolismo , Prenilação de Proteína/efeitos dos fármacos , Proteínas Proto-Oncogênicas p21(ras)/metabolismo , Sesquiterpenos , Células Tumorais Cultivadas/efeitos dos fármacos , Proteínas rac de Ligação ao GTP , Proteína rhoA de Ligação ao GTPRESUMO
We analyzed the effects of dietary cholesterol, type of dietary fat, sex and sire progeny family on lecithin-cholesterol acyltransferase activity in 80 adult baboons. The animals were the progeny of 80 dams and 6 sires and were randomly assigned at birth to breast feeding or to one of three formulas containing 0.02, 0.30 or 0.60 mg cholesterol/ml. After weaning at 4 months of age the animals were fed one of four diets that were either high or low in cholesterol with 40% of the calories from either saturated or unsaturated fat. The fractional and molar rates of lecithin-cholesterol acyltransferase activity were measured at 7-8 years of age by an HPLC method. Infant diet (breast vs. formula feeding or level of cholesterol in formula had no effect on enzyme activity later in life. The adult diets that were high in cholesterol decreased the fractional lecithin-cholesterol acyltransferase rate by 20% / compared to diets low in cholesterol (7.89 vs. 9.84%/h, P less than 0.002), but dietary cholesterol did not affect the molar activity. Animals fed the high cholesterol diets had higher unesterified cholesterol concentrations compared to those fed the low cholesterol diets (38.1 mg/dl vs. 31.6 mg/dl, P less than 0.0001). The molar lecithin-cholesterol acyltransferase rate was increased 13% by saturated compared to unsaturated fat (83.3 vs. 73.6 nmol/h per ml plasma, P less than 0.07), but no effect of dietary fat was observed on the fractional enzyme activity. Females compared to males had significantly higher fractional (10.9 vs. 7.14%/h, P less than 0.0001) and molar lecithin-cholesterol acyltransferase activities (99.3 vs. 61.7 nmol/h per ml plasma, P less than 0.0001). After adjustment for the effects of diet and sex we observed differences in the fractional activity (range, 7.2-10.8%/h, P less than 0.04) and in the molar rate (range, 63.6-99.8 nmol/h per ml plasma, P less than 0.07) among the six sire progeny groups. The differences among sire progeny groups are evidence for genetic differences in lecithin-cholesterol acyltransferase activities among the baboon families.
Assuntos
Colesterol na Dieta/farmacologia , Gorduras na Dieta/farmacologia , Fosfatidilcolina-Esterol O-Aciltransferase/sangue , Animais , Colesterol/sangue , Cromatografia Líquida de Alta Pressão , Feminino , Masculino , Papio , Fosfatidilcolina-Esterol O-Aciltransferase/genética , Fatores SexuaisRESUMO
We tested the hypothesis that breast and formula feeding differentially affect hepatic mRNA concentrations for LDL receptor (LDL-R) and apolipoproteins A-I, B and E in infant baboons during the preweaning period. The mRNA concentrations were measured in liver biopsies obtained prior to weaning at 14 weeks from 43 baboons that were either breast-fed (n = 17) or fed formulas with a high (n = 12) or low (n = 14) polyunsaturated/saturated (P:S) fat ratio. Breast-fed baboons had 99% higher LDL-R mRNA concentrations compared with infants fed formulas, but there were no differences among breast and formula-fed baboons in mRNA concentrations of apolipoproteins A-I, B or E. The fatty acid P:S ratio of the formulas did not affect hepatic LDL-R or apolipoprotein mRNA concentrations. These results suggest that breast-feeding increases LDL-R gene expression even though breast milk is higher in cholesterol and saturated fat compared with formulas.
Assuntos
Apolipoproteínas/análise , Aleitamento Materno , Gorduras na Dieta/administração & dosagem , Alimentos Formulados , Fígado/metabolismo , Receptores de LDL/análise , Animais , Animais Recém-Nascidos , Apolipoproteínas/genética , Colesterol/sangue , Feminino , Expressão Gênica , Lipoproteínas/sangue , Masculino , Papio , RNA Mensageiro/análise , Receptores de LDL/genética , DesmameRESUMO
26-Hydroxycholesterol (26OHC), a major oxysterol in human blood, is believed to play an important role in reverse cholesterol transport, bile acid formation, and regulation of various cellular processes. Using isotope dilution mass spectrometry, we measured plasma 26OHC concentrations in baboons fed either a high cholesterol/saturated fat (HC-SF) or normal chow diet. Plasma 26OHC levels in baboons were comparable to those reported for humans and were positively correlated with plasma cholesterol concentrations. Animals on the HC-SF diet had significantly higher 26OHC levels (0.274+/-0.058 microM, mean+/-S.D.) than those on the chow diet (0.156+/-0.046 microM). In separate experiments, [(3)H]26OHC was injected into four tethered baboons, and multiple blood samples drawn over a 1-h period were analyzed for [(3)H]26OHC and 26OHC. Fitting the specific radioactivity data to a two-pool compartmental model indicated a rapidly turning over plasma compartment (t(1/2) 2.9-6.0 min) and a second compartment with slow turnover (t(1/2) 76-333 min). The calculated 26OHC production rate was 2.5 micromol/kg body weight/day. Assuming all 26OHC is converted to bile acids, the 26OHC production rate corresponds to about 10% of total bile acid production in adult baboons. These results indicate that rapid turnover of plasma 26OHC at submicromolar concentrations could significantly contribute to bile acid synthesis.
Assuntos
Hidroxicolesteróis/sangue , Animais , Colesterol/sangue , Feminino , Cinética , Masculino , PapioRESUMO
Lovastatin, an inhibitor of protein prenylation, was reported to inhibit DNA synthesis and induce apoptosis in cultured cells. This report describes the morphological consequences of lovastatin treatment. Lovastatin (50 microM) induced mesangial cell rounding and disassembly of actin stress fibers within 24 to 48 h. After 48 to 72 h of lovastatin treatment, the cells detached from the substratum and underwent apoptotic cell death as evidenced by condensed nuclear chromatin, nuclear fragmentation, cell blebbing and decrease in cell size. Time lapse cinematography revealed that lovastatin caused cell rounding by either inhibiting cytokinesis or cell spreading following cytokinesis. Lovastatin-induced cell rounding, detachment, and apoptosis were dependent upon cell proliferation. These effects were prevented by serum deprivation to inhibit cell proliferation or by plating cells at densities which resulted in contact inhibition of cell growth. Lovastatin-induced mesangial cell rounding and apoptosis were also prevented by the inclusion of the isoprenoids all-trans-farnesol or all-trans-geranylgeraniol in the incubation medium. These results indicate that the effects of lovastatin were mediated by inhibition of protein isoprenylation because exogenous all-trans-geranylgeraniol can be used only in protein prenylation. The small GTP-binding protein RhoA, which may be important for cell spreading and cytokinesis, accumulated in the cytosol following treatment with lovastatin, suggestive of its inactivation. This effect was also prevented by the inclusion of either farnesol or geranylgeraniol in the incubation medium. Thus, lovastatin-induced apoptosis in mesangial cells occurs by interfering with prenylation dependent mitotic and post-mitotic events.
Assuntos
Apoptose/efeitos dos fármacos , Mesângio Glomerular/efeitos dos fármacos , Lovastatina/farmacologia , Mitose/efeitos dos fármacos , Actinas/metabolismo , Actinas/ultraestrutura , Animais , Bromodesoxiuridina/farmacologia , Contagem de Células/efeitos dos fármacos , Divisão Celular/efeitos dos fármacos , Movimento Celular/efeitos dos fármacos , Tamanho Celular/efeitos dos fármacos , Células Cultivadas , Diterpenos/farmacologia , Farneseno Álcool/farmacologia , Proteínas de Ligação ao GTP/metabolismo , Mesângio Glomerular/citologia , Microscopia Eletrônica , Microscopia de Vídeo , Prenilação de Proteína/efeitos dos fármacos , Ratos , Proteína rhoA de Ligação ao GTPRESUMO
Atherosclerosis and coronary heart disease are promoted by elevated serum low density lipoprotein cholesterol (LDL-C) and are retarded by increased high density lipoprotein cholesterol (HDL-C). Considerable variability in these lipoproteins has been observed in studies of captive animals subjected to extensive experimental manipulations, or by epidemiological studies of human beings. We have examined these variables in wild male baboons living undisturbed in their natural habitat in the Serengeti Ecosystem of East Africa. Among socially subordinate males, HDL-C and apolipoprotein A-I concentrations were significantly reduced by 31% and 25%, respectively, compared to concentrations in dominant individuals. There were no social rank differences in VLDL + LDL-C or its apolipoprotein (Apo B). Differences in age, sex hormone concentrations, rank-related diet, body weight, or gene pools were unlikely to explain this rank-related pattern. However, diminished HDL-C concentrations were associated with elevated basal cortisol concentrations, suggesting that exposure of subordinate individuals to elevated levels of social stressors could cause lower HDL-C concentrations.
Assuntos
HDL-Colesterol/sangue , Dominação-Subordinação , Papio/fisiologia , Predomínio Social , Estresse Psicológico/sangue , Envelhecimento , Animais , Animais Selvagens , Dexametasona/farmacologia , Masculino , Metirapona/farmacologia , Maturidade SexualRESUMO
We previously reported that female baboons overfed during infancy were not fatter at weaning, but developed hypertrophic obesity after puberty. To clarify the mechanisms of this dietary effect on adipocyte hypertrophy, we determined the effects of infant overfeeding on preweaning plasma hormone and triglyceride levels and their relationship with fat cell volume at weaning (19 weeks of age). Newborn female baboons from 3 sires and 24 dams were fed either 280 kilojoules (normally fed; n = 12) or 395 kilojoules (overfed; n = 10) per 100 g Similac formula for 18 weeks. Both formulas contained 9.2%, 43.1%, and 48.5% of calories as protein, carbohydrate, and fat, respectively. During the first 9 weeks, overfed infants had significantly higher fasting and postprandial insulin, total T3, and free T3 concentrations; lower cortisol levels; and lower excretion of urinary 17-hydroxycorticosteroids (17-OHCS) than normally fed infants. These effects were no longer significant at 17-18 weeks. Infant diet did not influence fasting and postprandial plasma triglyceride levels, and fat cell volume was not influenced by energy intake. However, fat cell volume was positively associated with postprandial triglyceride concentrations and inversely associated with postmeal nadir cortisol levels. These results demonstrate that infant overfeeding initiates early alterations in insulin, T3, free T3, and cortisol, but these effects persist only as long as there is a significant increase in energy intake.
Assuntos
Animais Recém-Nascidos/sangue , Metabolismo Energético/fisiologia , Alimentos Formulados , Hidrocortisona/sangue , Insulina/sangue , Papio/sangue , Hormônios Tireóideos/sangue , Triglicerídeos/sangue , 17-Hidroxicorticosteroides/urina , Animais , Estatura/efeitos dos fármacos , FemininoRESUMO
We measured the effects of dietary cholesterol (0.24 vs 0.0024 mg/kJ), type of dietary fat [saturated, a ratio of polyunsaturated to saturated fatty acids (P:S) of 0.37, vs unsaturated (P:S of 2.2)], and sex on biliary lipid and bile acid conjugate composition of 80 adult pedigreed baboons. From these data we calculated the bile cholesterol saturation index and the bile acid hydrophobicity index. Dietary cholesterol significantly increased the bile cholesterol concentration by 25% and the bile cholesterol saturation index by 15%, but did not significantly affect the bile acid conjugate composition or the bile acid hydrophobicity index. Diets high in saturated fatty acid compared with unsaturated fatty acid significantly decreased the bile cholesterol concentrations by 26% and the saturation index by 23%. Saturated fatty acid also decreased the proportion of hydrophobic bile acids and lowered the bile hydrophobicity index. Male baboons had a higher cholesterol saturation index and a lower hydrophobicity index than females. Dietary cholesterol and saturated fatty acid independently influence the bile lipid composition and the cholesterol saturation index.
Assuntos
Bile/química , Gorduras na Dieta/farmacologia , Caracteres Sexuais , Animais , Colesterol/análise , Colesterol na Dieta/administração & dosagem , Colesterol na Dieta/farmacologia , Gorduras na Dieta/administração & dosagem , Ácidos Graxos/farmacologia , Feminino , Masculino , Fosfolipídeos/análiseRESUMO
Genetic effects on serum lipoprotein and apoprotein concentrations were investigated using a paternal half-sib design with 79 progeny of 6 sires. Significant differences (P less than 0.05) were observed among sire progeny groups at 4-6 years of age for serum cholesterol, HDL cholesterol and apoA-I concentrations. A sire effect (P less than 0.10) also was observed for VLDL + LDL cholesterol concentrations, but differences were not observed (P greater than 0.10) among sire progeny groups for apoB concentrations. Estimates of heritability were 0.54 for serum cholesterol, 0.32 for VLDL + LDL cholesterol, 0.78 for HDL cholesterol, 0.56 for apoA-I, and 0.20 for apoB concentration. Genetic (rg) and environmental (re) correlations among serum cholesterol, lipoprotein cholesterol, and apoprotein concentrations were positive except for the negative genetic relationships of apoA-I with apoB (rg = -0.74) and with VLDL + LDL cholesterol (rg = -0.30) concentrations. The phenotypic correlation (rp = 0.31) of VLDL + LDL cholesterol with HDL cholesterol was due entirely to the genetic contribution (0.31) since the environmental contribution was zero. The positive genetic relationship (rg = 0.62) of VLDL + LDL cholesterol and HDL cholesterol may be due to biochemical mechanisms controlling cholesterol turnover since the genetic correlations of VLDL + LDL cholesterol and HDL cholesterol with cholesterol turnover rate were both negative (-0.43 and -0.68, respectively). A strong negative genetic correlation (rg = -0.95) was observed between apoA-I and cholesterol turnover, a finding that suggests a close physiologic relationship between these variables.
Assuntos
Apolipoproteínas/sangue , Colesterol/sangue , Lipoproteínas/sangue , Papio/genética , Animais , Apolipoproteína A-I , Apolipoproteínas B , Papio/sangueRESUMO
We investigated the effects of a polymorphic PvuII site in the gene for lecithin:cholesterol acyltransferase (LCAT) on serum high density lipoprotein cholesterol (HDL-C) and apolipoprotein A-I (apo A-I) concentrations in a population of 750 pedigreed baboons. We also tested for genotype by diet interactions using data on HDL-C and apo A-I concentrations on two diets (chow and high-cholesterol, saturated fat). A significant (P < 0.001) association between the LCAT genotypes and HDL-C levels was observed. On both diets, animals homozygous for the less common allele had HDL-C levels that averaged 18-19% lower than animals homozygous for the more common allele. HDL-C levels of the heterozygotes were intermediate. The LCAT RFLP accounted for approximately 5% of the variation in HDL-C levels on the two diets. We observed no strong evidence for an LCAT genotype by diet interaction effect.
Assuntos
HDL-Colesterol/sangue , DNA/genética , Fosfatidilcolina-Esterol O-Aciltransferase/genética , Polimorfismo Genético , Alelos , Animais , Apolipoproteína A-I/análise , Gorduras na Dieta/administração & dosagem , Feminino , Genótipo , Masculino , Papio , Especificidade da EspécieRESUMO
The long-term effects of infant diet (breast milk or formula containing 2, 30, or 60 mg/dl cholesterol) and subsequent dietary cholesterol (1 mg/kcal) and fat (saturated or unsaturated) on serum lipid and apolipoprotein concentrations were estimated using 82 juvenile baboons 4-6 years of age. A significant interaction of infant diet (breast vs formula) with type of fat (saturated vs unsaturated) at 4-6 years of age was observed on HDL cholesterol and apolipoprotein A-I (apoA-I) concentrations. That is, animals breast-fed as infants had higher HDL cholesterol and apoA-I concentrations when fed unsaturated fat from weaning to 4-6 years of age than those fed saturated fat (77 vs 68 mg/dl). In contrast, animals fed formulas in infancy followed by a diet containing unsaturated fat had lower HDL cholesterol and apoA-I concentrations at 4-6 years of age than did those fed saturated fat (67 vs 78 mg/dl). However, breast feeding or feeding formulas containing various levels of cholesterol for 3 months during infancy did not result in statistically significant differences in total serum cholesterol, VLDL + LDL cholesterol and apolipoprotein B (apoB) concentrations. Dietary cholesterol after infancy significantly increased serum total cholesterol, VLDL + LDL and HDL cholesterol, apoA-I and apoB concentrations. All of these response variables also were higher in animals fed saturated fat compared to those fed unsaturated fat on the same level of cholesterol. At 4-6 years of age, regardless of diet, females had significantly higher serum VLDL + LDL cholesterol (57 vs 43 mg/dl) and apoB concentrations (39 vs 30 mg/dl) than did males.
Assuntos
Envelhecimento , Apolipoproteínas/sangue , Colesterol/sangue , Dieta , Animais , Colesterol na Dieta/administração & dosagem , HDL-Colesterol , LDL-Colesterol , VLDL-Colesterol , Feminino , Alimentos Infantis , Lactação , Lipoproteínas/sangue , Lipoproteínas HDL/sangue , Lipoproteínas LDL/sangue , Lipoproteínas VLDL/sangue , Masculino , Papio , GravidezRESUMO
The effects of 2 different dietary fats (40% of calories from corn oil or coconut oil), in the presence of high-dietary cholesterol (1.7 mg/kcal), on the lipoprotein profiles of baboons (Papio cynocephalus sp) were studied by analytic ultracentrifugation, gradient gel electrophoresis (GGE), and heparin-manganese chloride precipitation. Relative to the corn oil (polyunsaturated fat) diet, the coconut oil (saturated fat) diet significantly increased total serum cholesterol by 43% (P less than 0.001) by increasing non-precipitable cholesterol (HDL-C) 58% (P less than 0.001) and precipitable cholesterol (VLDL + LDL-C) 35% (P less than 0.001). Analytic ultracentrifugal observations indicated that the increase in HDL-C was due to considerable increases in both HDL-I (baboon HDL of size 100-125 A and hydrated density 1.063-1.120 g/ml) and F1.20 degrees 9-28 lipoproteins (material of size 125-220 A and hydrated density 1.03-1.08 g/ml, and containing HDL apolipoproteins and apo E). Concentrations of other HDL subpopulations were unaffected by the dietary saturated rat. The increase in VLDL + LDL-C was due to increased LDL (S degree F 5-12 lipoproteins) and, to some extent, F1.20 degrees 9-28 lipoproteins because the larger, faster floating subspecies of the F1.20 degrees 9-28 lipoproteins were precipitable by heparin-manganese. In contrast, saturated fat (relative to polyunsaturated fat) induced lower concentrations of IDL (SF degree 12-20) and VLDL (SF degree 20-100). Lipoprotein size distributions by GGE indicated 5 HDL subpopulations and 2 or more LDL subpopulations in the sera of most baboons. The type of dietary fat did not affect the particle size range of each of the the HDL or LDL subpopulations. The results indicate that dietary fat markedly modulates the distribution of cholesterol between apo A-I-containing (HDL and F1.20 degrees 9-28) and apo B-containing (IDL and VLDL) lipoproteins without altering the presence of subpopulations based on particle size.
Assuntos
Gorduras na Dieta/farmacologia , Gorduras Insaturadas/farmacologia , Lipoproteínas/sangue , Animais , Colesterol/sangue , HDL-Colesterol/sangue , LDL-Colesterol/sangue , Feminino , Lipoproteínas HDL/sangue , Lipoproteínas IDL , Lipoproteínas LDL/sangue , Lipoproteínas VLDL/sangue , Masculino , Papio , Tamanho da PartículaRESUMO
We examined the results of one generation of selection for serum cholesterol (SC) concentration on low density lipoprotein cholesterol (LDL-C), high density lipoprotein cholesterol (HDL-C), and triglyceride concentrations and weight in baboons (Papio cynocephalus). Parents of two lines (high SC response and low SC response) were chosen based on their SC response to a 4-month challenge with a cholesterol and saturated fat enriched diet. Parents of the control line were chosen without regard for SC levels. Expression of SC, LDL-C, and HDL-C concentrations was moderately influenced by additive genetic effects as evidenced by the direct and correlated responses of the serum lipoprotein concentrations of the juvenile offspring of the three lines. Realized heritability of SC and genetic correlations of SC with LDL-C and HDL-C were moderate to high. Sex and age were important factors influencing expression of SC, LDL-C, HDL-C, triglycerides, and weight in both adult baboons and their offspring.
Assuntos
Colesterol/sangue , Papio/sangue , Animais , Peso Corporal , Colesterol na Dieta/administração & dosagem , HDL-Colesterol/sangue , LDL-Colesterol/sangue , Dieta Aterogênica , Feminino , Masculino , Papio/genética , Seleção Genética , Triglicerídeos/sangueRESUMO
In a series of experiments over the past 20 years, we have demonstrated long-term deferred effects of infant nutrition, particularly breast- as compared with formula-feeding and overfeeding as compared with normal or underfeeding, on serum HDL-cholesterol concentrations, adiposity, and atherosclerosis in the baboon, a large nonhuman primate. Low HDL-cholesterol levels and obesity are associated with accelerated progression of atherosclerosis and with increased risk of coronary heart disease in humans. We have observed other deferred effects of infant nutrition on bile acid metabolism, enzyme activities, and water and electrolyte balance, some of which may be physiologically related to HDL-cholesterol levels or to adiposity. The occurrence of these deferred effects suggests that infant nutrition may program other metabolic systems for life, and that these effects may contribute to other chronic diseases of adults. Although our understanding of the mechanisms by which infant diet regimens affect adult metabolism is meager, it is important to identify these mechanisms because they are likely to provide valuable clues to the causes and ultimately may contribute to the long-range prevention of those diseases.
Assuntos
Doenças Cardiovasculares/etiologia , Fenômenos Fisiológicos da Nutrição do Lactente , Lipídeos/sangue , Lipoproteínas/sangue , Adulto , Animais , Criança , Pré-Escolar , Gorduras na Dieta/administração & dosagem , Feminino , Humanos , Lactente , Masculino , PapioRESUMO
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.