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1.
Br J Nutr ; 131(4): 630-641, 2024 02 28.
Artigo em Inglês | MEDLINE | ID: mdl-37795821

RESUMO

The offspring of women in the poorest socio-economic groups in Western societies have an increased risk of developing non-communicable disease in adult life. Deprivation is closely related to the consumption of a diet with an excess of energy (sugar and fat), salt and a shortage of key vitamins. To test the hypothesis that this diet adversely affects the development and long-term health of the offspring, we have formulated two rodent diets, one with a nutrient profile corresponding to the diet of pregnant women in the poorest socio-economic group (DEP) and a second that incorporated current UK recommendations for the diet in pregnancy (REC). Female rats were fed the experimental diets for the duration of gestation and lactation and the offspring compared with those from a reference group fed the AIN-93G diet. The growth trajectory of DEP and REC offspring was reduced compared with the AIN-93G. The REC offspring diet had a transient increase in adipose reserves at weaning, but by 30 weeks of age the body composition of all three groups was similar. The maternal diet had no effect on the homoeostatic model assessment index or the insulin tolerance of the offspring. Changes in hepatic gene expression in the adult REC offspring were consistent with an increased hepatic utilisation of fatty acids and a reduction in de novo lipogenesis. These results show that despite changes in growth and adiposity maternal metabolic adaptation minimises the adverse consequences of the imbalanced maternal diet on the metabolism of the offspring.


Assuntos
Obesidade , Efeitos Tardios da Exposição Pré-Natal , Humanos , Ratos , Animais , Feminino , Gravidez , Peso Corporal , Obesidade/metabolismo , Dieta , Adiposidade , Fígado/metabolismo , Desmame , Lactação , Dieta Hiperlipídica/efeitos adversos , Fenômenos Fisiológicos da Nutrição Materna , Efeitos Tardios da Exposição Pré-Natal/metabolismo
2.
Microbiome ; 12(1): 89, 2024 May 14.
Artigo em Inglês | MEDLINE | ID: mdl-38745230

RESUMO

BACKGROUND: Non-toxic approaches to enhance radiotherapy outcomes are beneficial, particularly in ageing populations. Based on preclinical findings showing that high-fibre diets sensitised bladder tumours to irradiation by modifying the gut microbiota, along with clinical evidence of prebiotics enhancing anti-cancer immunity, we hypothesised that dietary fibre and its gut microbiota modification can radiosensitise tumours via secretion of metabolites and/or immunomodulation. We investigated the efficacy of high-fibre diets combined with irradiation in immunoproficient C57BL/6 mice bearing bladder cancer flank allografts. RESULT: Psyllium plus inulin significantly decreased tumour size and delayed tumour growth following irradiation compared to 0.2% cellulose and raised intratumoural CD8+ cells. Post-irradiation, tumour control positively correlated with Lachnospiraceae family abundance. Psyllium plus resistant starch radiosensitised the tumours, positively correlating with Bacteroides genus abundance and increased caecal isoferulic acid levels, associated with a favourable response in terms of tumour control. Psyllium plus inulin mitigated the acute radiation injury caused by 14 Gy. Psyllium plus inulin increased caecal acetate, butyrate and propionate levels, and psyllium alone and psyllium plus resistant starch increased acetate levels. Human gut microbiota profiles at the phylum level were generally more like mouse 0.2% cellulose profiles than high fibre profiles. CONCLUSION: These supplements may be useful in combination with radiotherapy in patients with pelvic malignancy. Video Abstract.


Assuntos
Fibras na Dieta , Suplementos Nutricionais , Microbioma Gastrointestinal , Inulina , Camundongos Endogâmicos C57BL , Psyllium , Neoplasias da Bexiga Urinária , Animais , Camundongos , Microbioma Gastrointestinal/efeitos dos fármacos , Inulina/administração & dosagem , Neoplasias da Bexiga Urinária/radioterapia , Neoplasias da Bexiga Urinária/patologia , Humanos , Feminino , Lesões por Radiação/prevenção & controle , Intestinos/microbiologia , Intestinos/efeitos da radiação , Linfócitos T CD8-Positivos
3.
J Nutr ; 141(1): 95-100, 2011 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21106931

RESUMO

Methyl deficiencies have been implicated in metabolic programming during the periods of oocyte and embryo development. Semisynthetic methyl-deficient diets (MD) with no folic acid, 0.05% choline, and approximately one-half the recommended content of methionine were fed to female rats for 3 wk prior to mating and for the first 5 d of gestation. During the period of MD feeding, plasma homocysteine concentrations were approximately twice those of rats fed the complete (CON) diet. From d 5, both groups received a complete semipurified AIN diet until birth. On d 8, plasma homocysteine concentrations did not differ between the 2 groups. Thereafter, dams and offspring were fed a nonpurified diet for the remainder of the experiment. At 6 mo of age, the homeostatic model assessment (HOMA) index of the male MD offspring tended to be 32% higher (P = 0.053) and peak insulin during an oral glucose tolerance test (oGTT) was 39% higher (P < 0.05) compared with the male CON offspring. There was no difference in the response to an oGTT in the female offspring at 6 mo of age. The increased HOMA index of male MD offspring persisted to 12 mo of age. The peak glucose concentration during oGTT was 23% higher (P < 0.05) in MD compared with the CON males despite 39% greater (P < 0.05) peak insulin concentrations. This study shows that in rats, a physiologically relevant methyl-deficient diet fed during the period of oocyte maturation and preimplantation development programs gender-specific changes in glucose handling by the offspring.


Assuntos
Glucose/metabolismo , Homeostase , Desnutrição/metabolismo , Fenômenos Fisiológicos da Nutrição Materna/fisiologia , Animais , Glicemia/análise , Deficiência de Colina/metabolismo , Feminino , Teste de Tolerância a Glucose , Homocisteína/sangue , Insulina/sangue , Masculino , Metilação , Estado Nutricional , Ratos , Caracteres Sexuais
4.
J Dev Orig Health Dis ; 11(3): 264-272, 2020 06.
Artigo em Inglês | MEDLINE | ID: mdl-31543090

RESUMO

Iron deficiency is common in pregnant and lactating women and is associated with reduced cognitive development of the offspring. Since iron affects lipid metabolism, the availability of fatty acids, particularly the polyunsaturated fatty acids required for early neural development, was investigated in the offspring of female rats fed iron-deficient diets during gestation and lactation. Subsequent to the dams giving birth, one group of iron-deficient dams was recuperated by feeding an iron-replete diet. Dams and neonates were killed on postnatal days 1, 3 and 10, and the fatty acid composition of brain and stomach contents was assessed by gas chromatography. Changes in the fatty acid profile on day 3 became more pronounced on day 10 with a decrease in the proportion of saturated fatty acids and a compensatory increase in monounsaturated fatty acids. Long-chain polyunsaturated fatty acids in the n-6 family were reduced, but there was no change in the n-3 family. The fatty acid profiles of neonatal brain and stomach contents were similar, suggesting that the change in milk composition may be related to the changes in the neonatal brain. When the dams were fed an iron-sufficient diet at birth, the effects of iron deficiency on the fatty acid composition of lipids in both dam's milk and neonates' brains were reduced. This study showed an interaction between maternal iron status and fatty acid composition of the offspring's brain and suggests that these effects can be reduced by iron repletion of the dam's diet at birth.


Assuntos
Anemia Ferropriva/complicações , Encéfalo/crescimento & desenvolvimento , Metabolismo dos Lipídeos/fisiologia , Complicações Hematológicas na Gravidez/fisiopatologia , Efeitos Tardios da Exposição Pré-Natal/patologia , Anemia Ferropriva/fisiopatologia , Animais , Animais Recém-Nascidos/metabolismo , Animais Lactentes/metabolismo , Encéfalo/patologia , Química Encefálica/fisiologia , Modelos Animais de Doenças , Ácidos Graxos Ômega-3/análise , Ácidos Graxos Ômega-3/metabolismo , Ácidos Graxos Ômega-6/análise , Ácidos Graxos Ômega-6/metabolismo , Feminino , Humanos , Ferro/sangue , Deficiências de Ferro , Lactação/fisiologia , Masculino , Gravidez , Efeitos Tardios da Exposição Pré-Natal/etiologia , Efeitos Tardios da Exposição Pré-Natal/metabolismo , Ratos
5.
Br J Nutr ; 101(9): 1333-40, 2009 May.
Artigo em Inglês | MEDLINE | ID: mdl-18782463

RESUMO

In humans poor maternal folate status is associated with a decrease in infant birth weight. As low birth weight increases the risk of cardiovascular and metabolic disease in adults, an inadequate supply of folic acid in the mother's diet may increase the susceptibility of the offspring to disease. We have fed laboratory rats diets deficient in folic acid and the related methyl donors methionine and choline to examine the effects on growth, blood pressure and insulin action in the offspring. Poor folate status transiently increased fetal growth but did not produce a long-term change in body weight. There were, however, small changes in the hearts of the female offspring. When folate deficiency was combined with low intakes of methionine and choline, the kidneys of the male offspring were proportionately smaller, probably because of the limited availability of methionine. There was no effect on the blood pressure of either the male or female offspring. The pancreatic insulin content of fetuses from animals fed the folate-deficient diets were higher than those of the controls. Following an oral glucose challenge, there was a weak trend for glucose-stimulated insulin release to be increased in the offspring of dams fed the folate-deficient diet. The changes in insulin concentrations were, however, much smaller than the corresponding changes observed in the offspring of animals fed protein-deficient diets. These results suggest that folate deficiency during gestation causes modest changes to the insulin axis of the fetus.


Assuntos
Pressão Sanguínea/fisiologia , Deficiência de Colina/fisiopatologia , Deficiência de Ácido Fólico/fisiopatologia , Metionina/deficiência , Fenômenos Fisiológicos da Nutrição Pré-Natal/fisiologia , Acetil-CoA Carboxilase/metabolismo , Animais , Carnitina O-Palmitoiltransferase/metabolismo , Deficiência de Colina/metabolismo , Ingestão de Alimentos/fisiologia , Feminino , Desenvolvimento Fetal/fisiologia , Peso Fetal/fisiologia , Deficiência de Ácido Fólico/metabolismo , Teste de Tolerância a Glucose , Crescimento/fisiologia , Insulina/metabolismo , Masculino , Tamanho do Órgão/fisiologia , Pâncreas/embriologia , Pâncreas/metabolismo , Gravidez , Complicações na Gravidez/fisiopatologia , Ratos
6.
Br J Nutr ; 102(10): 1445-52, 2009 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-19566968

RESUMO

Previously we have examined the effects of diets deficient in folic acid ( - F) or folate deficient with low methionine and choline ( - F LM LC) on the relative abundance of soluble proteins in the liver of the pregnant rat. In the present study we report the corresponding changes in the fetal liver at day 21 of gestation. The abundance of eighteen proteins increased when dams were fed the - F diet. When dams were fed the - F LM LC diet, thirty-three proteins increased and eight decreased. Many of the differentially abundant proteins in the fetal liver could be classified into the same functional groups as those previously identified in the maternal liver, namely protein synthesis, metabolism, lipid metabolism and proteins associated with the cytoskeleton and endoplasmic reticulum. The pattern was consistent with reduced cell proliferation in the - F LM LC group but not in the - F group. Metabolic enzymes associated with lipid metabolism changed in both the - F and - F LM LC groups. The mRNA for carnitine palmitoyl transferase were up-regulated and CD36 (fatty acid translocase) down-regulated in the - F group, suggesting increased mitochondrial oxidation of fatty acids as an indirect response to altered maternal lipid metabolism. In the - F LM LC group the mRNA for acetyl CoA carboxylase was down-regulated, suggesting reduced fatty acid synthesis. The mRNA for transcriptional regulators including PPARalpha and sterol response element-binding protein-1c were unchanged. These results suggest that an adequate supply of folic acid and the related methyl donors may benefit fetal development directly by improving lipid metabolism in fetal as well as maternal tissues.


Assuntos
Dieta , Ácido Fólico/farmacologia , Metabolismo dos Lipídeos/fisiologia , Fígado/embriologia , Fígado/metabolismo , Ração Animal , Animais , Feminino , Feto , Deficiência de Ácido Fólico , Regulação da Expressão Gênica/fisiologia , Fenômenos Fisiológicos da Nutrição Materna , Gravidez , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Ratos
7.
Metabolism ; 55(6): 763-70, 2006 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-16713436

RESUMO

The pregnant rat fed a low-protein diet has become widely used as a model system in the study of the prenatal programming of adult metabolism and disease. When pregnant rats of the hooded Lister strain were fed semisynthetic diets containing 18% or 9% casein supplemented with 0.5% dl-methionine, there was significant postnatal mortality in the group fed the low-protein diet. In a second experiment, dams were fed diets containing 9% casein supplemented with varying concentrations of dl-methionine up to 0.4% (w/w) and compared with a group fed a diet containing 18% casein supplemented with 0.5% dl-methionine. At birth, the pups from dams fed the low-protein diets supplemented with 0.2% dl-methionine or greater were significantly smaller than those of the dams fed the diet containing 18% protein. By 25 weeks of age, the body weight of the offspring of dams fed the low-protein diet supplemented with 0.2% or 0.3% dl-methionine were approximately 10% lower than those in the control group of offspring from dams fed 18% protein supplemented with 0.5% dl-methionine. There were corresponding changes in the weights of the major organs. These data suggest that increasing the dl-methionine supplement in the low-protein diet retards the growth of the fetus and affects the mature adult body weight. In contrast to the findings of other studies that used different formulas of the low-protein diet, the glucose tolerance in the offspring was unaffected by the protein content of the maternal diet at all levels of dl-methionine supplementation. These results suggest that the changes in metabolism of the offspring result from interactions between protein, lipids, and carbohydrates in the maternal diet, rather than a consequence of postnatal growth retardation per se and highlight the importance of considering all components of the maternal diet in the programming mechanism.


Assuntos
Dieta , Crescimento/efeitos dos fármacos , Exposição Materna , Metionina/farmacologia , Animais , Pressão Sanguínea , Peso Corporal , Caseínas/administração & dosagem , Caseínas/farmacologia , Proteínas Alimentares/administração & dosagem , Proteínas Alimentares/farmacologia , Feminino , Teste de Tolerância a Glucose , Masculino , Metionina/administração & dosagem , Tamanho do Órgão , Gravidez , Ratos , Ratos Endogâmicos , Fatores Sexuais
8.
Metabolism ; 55(5): 642-9, 2006 May.
Artigo em Inglês | MEDLINE | ID: mdl-16631441

RESUMO

Evidence to support an association between early nutrition and the development of obesity in the rat is equivocal. In this study we have investigated the postnatal growth, glucose tolerance, and adipocyte function of the offspring from pregnant rats fed with diets containing either 20% or 8% protein during gestation. By 25 weeks of age, the female offspring of dams fed with the diet containing 8% protein had a significantly lower adult body weight due in part to a decrease in body fat. The peak concentration of insulin after oral administration of a glucose dose was significantly lower in both the male and female offspring of the dams fed with the diet containing 8% protein. However, the ability of insulin to stimulate lipogenesis or suppress lipolysis in fat cells isolated from the offspring was not influenced by the prenatal diet. Hepatic phosphoenolpyruvate carboxykinase activity was reduced in female offspring of dams fed with the diet containing 8% protein. These results show that adult body composition is determined during the prenatal period as a result of programming of the insulin axis. This metabolic programming influences hepatic metabolism; however, there is no evidence for a programmed change in adipocyte function.


Assuntos
Composição Corporal/efeitos dos fármacos , Proteínas Alimentares/farmacologia , Desenvolvimento Fetal/efeitos dos fármacos , Insulina/metabolismo , Efeitos Tardios da Exposição Pré-Natal , Adipócitos/metabolismo , Animais , Animais Recém-Nascidos , Glicemia/metabolismo , Composição Corporal/fisiologia , Peso Corporal/fisiologia , Proteínas Alimentares/metabolismo , Feminino , Desenvolvimento Fetal/fisiologia , Glucoquinase/metabolismo , Teste de Tolerância a Glucose , Fígado/enzimologia , Fígado/metabolismo , Masculino , Fosfoenolpiruvato Carboxiquinase (ATP)/metabolismo , Gravidez , Ratos , Ratos Long-Evans
9.
Physiol Rep ; 4(21)2016 11.
Artigo em Inglês | MEDLINE | ID: mdl-27905292

RESUMO

Iron is essential for the oxidative metabolism of lipids. Lipid metabolism changes during gestation to meet the requirements of the growing fetus and to prepare for lactation. The temporal effects of iron deficiency during gestation were studied in female rats fed complete or iron-deficient diets. Plasma triglycerides were elevated in the iron-deficient group throughout gestation. There were time-dependent changes in the triglyceride content of the maternal liver, falling at the midpoint of gestation and then increasing on d21.5. Compared to the control, triglycerides in the maternal liver were not different in the iron-deficient group prior to pregnancy and on d12.5, but were markedly reduced by d21.5. The abundance of mRNAs in the maternal liver suggests that lipogenesis is unchanged and beta-oxidation is reduced on d21.5 by iron deficiency. On d21.5 of gestation, the expression of placental lipase was unchanged by iron deficiency, however, the abundance of mRNAs for SREBP-1c, FABP4 were reduced, suggesting that there were changes in fatty acid handling. In the fetal liver, iron deficiency produced a marked decrease in the abundance of the L-CPT-1 mRNA, suggesting that beta-oxidation is reduced. This study shows that the major effect of iron deficiency on maternal lipid metabolism occurs late in gestation and that perturbed lipid metabolism may be a common feature of models of fetal programming.


Assuntos
Desenvolvimento Fetal/fisiologia , Deficiências de Ferro , Ferro/metabolismo , Metabolismo dos Lipídeos/genética , Fígado/metabolismo , Fenômenos Fisiológicos da Nutrição Pré-Natal/genética , Triglicerídeos/sangue , Animais , Proteínas de Ligação a Ácido Graxo/metabolismo , Feminino , Feto/metabolismo , Ferro/efeitos adversos , Lactação/fisiologia , Lipogênese/fisiologia , Fígado/embriologia , Fígado/enzimologia , Placenta/enzimologia , Placenta/metabolismo , Gravidez/metabolismo , RNA Mensageiro/metabolismo , Ratos , Proteína de Ligação a Elemento Regulador de Esterol 1/metabolismo
10.
Genes Nutr ; 9(1): 380, 2014 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-24382649

RESUMO

The mechanisms by which maternal protein deficiency programs insulin action in the offspring are poorly understood. The interpretation of transcriptomics is complicated by homeostatic adaptations, for example, changes in amino acid metabolism, which are potentially unrelated to the programming mechanism. The fatty acid composition of the maternal diet modulates the programming of insulin action, offering a possible strategy to circumvent these complications. Fetal livers harvested on d21 of gestation from pregnant rats fed high-protein (18 % w/w) and low-protein (9 % w/w) diets prepared with either corn or soya oil were screened with rat genome microarrays. Although a low-protein maternal diet altered the abundance of more than one hundred mRNAs in the fetal liver, only 40 were changed by the fatty acid composition of the diet (P < 0.05). One of these mRNAs was identified as lipocalin-2 (Lcn2). This pattern of differential expression was confirmed by qRT-PCR. The expression of Lcn2 was decreased by low-protein diets when the diet contained soya oil, whereas the effect of protein was much smaller in the group fed diets prepared with corn oil. The decrease in Lcn2 expression produced by soya oil persisted into adult life. Levels of the Lcn2 protein were closely correlated to the mRNA abundance. The results suggest a possible involvement of Lcn2 in the programming of hepatic function.

11.
Genes Nutr ; 8(2): 181-90, 2013 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-22907820

RESUMO

A methyl-deficient diet (MD) lacking folic acid and the associated methyl donors choline and methionine, fed to the laboratory rat during the periods of oocyte and embryo development, has been shown to programme glucose metabolism in the offspring. The hepatic proteome of the male offspring of female rats fed MD diets for 3 weeks prior to mating and for the first 5 days of gestation has been examined by 2-dimensional gel electrophoresis. Three groups of differentially abundant proteins associated with energy metabolism, amino acid metabolism and antioxidant defence were identified in the soluble proteins extracted from the liver from the MD offspring at both 6 and 12 months of age. Altered mitochondrial activity in other programming models leads to a similar pattern of differential protein abundance. Two of the differentially abundant proteins were identified as GAPDH and PGK-1 by mass spectrometry. Western blotting showed that there were multiple isoforms of both proteins with similar molecular weights but different isoelectric points. The differentially abundant spots reduced in the MD offspring corresponded to minor isoforms of GAPDH and PGK-1. The levels of PPAR-alpha, SREBP and glucocorticoid receptor mRNAs associated with other models of prenatal programming were unchanged in the MD offspring. The data suggest that a diet deficient in folic acid and associated methyl donors fed during the peri-conception and early preimplantation periods of mammalian development affects mitochondrial function in the offspring and that the posttranslational modification of proteins may be important.

12.
Genes Nutr ; 4(3): 189-94, 2009 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-19484284

RESUMO

Foetal growth is particularly sensitive to the protein content of the mother's diet. Microarray data from the foetal liver of pregnant rats fed normal (HP) or reduced protein diets (LP) were compared by gene set enrichment analysis. Soluble proteins from a second portion of the liver were analysed by two-dimensional gel electrophoresis. Genes associated with progesterone, insulin-like growth factor-1 and vascular endothelial growth factor were upregulated in HP compared to LP, in addition to genes associated with cell differentiation and signalling from the extracellular matrix. In contrast, cytokine signalling was downregulated. Proteomics showed that proteins associated with amino acid metabolism, mitochondrial function and cell motility were differentially abundant in the HP compared to the LP groups. These growth factor and extracellular matrix signalling pathways linked to cell motility may be important mediators of the changes in liver structure that occur in utero and persist into adult life.

13.
Br J Nutr ; 99(2): 262-71, 2008 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-17697402

RESUMO

The importance of folic acid and the methionine cycle in fetal development is well recognised even though the mechanism has not been established. Since the cycle is active in the maternal liver, poor folate status may modify hepatic metabolism. Pregnant rats were fed diets deficient in folic acid (-F) or in three key methyl donors, folic acid, choline and methionine (-FLMLC) and the maternal liver was analysed on day 21 of gestation. Two-dimensional gel electrophoresis of soluble proteins identified differentially abundant proteins, which could be allocated into nine functional groups. Five involved in metabolic processes, namely, folate/methionine cycle, tyrosine metabolism, protein metabolism, energy metabolism and lipid metabolism, and three in cellular processes, namely, endoplasmic reticulum function, bile production and antioxidant defence. The mRNA for sterol regulatory element-binding protein-1c and acetyl-CoA carboxylase-1 (fatty acid synthesis) were decreased by both -F and -FLMLC diets. The mRNA for PPARalpha and PPARgamma and carnitine palmitoyl transferase (fatty acid oxidation) were increased in the animals fed the -FLMLC diets. Changes in the abundance of proteins associated with intracellular lipid transport suggest that folate deficiency interferes with lipid export. Reduced fatty acid synthesis appeared to prevent steatosis in animals fed the -F diet. Even with increased oxidation, TAG concentrations were approximately three-fold higher in animals fed the -FLMLC diet and were associated with an increase in the relative abundance of proteins associated with oxidative stress. Fetal development may be indirectly affected by these changes in hepatic lipid metabolism.


Assuntos
Dieta , Deficiência de Ácido Fólico/metabolismo , Metabolismo dos Lipídeos , Fígado/metabolismo , Gravidez/metabolismo , Fenômenos Fisiológicos da Nutrição Pré-Natal/fisiologia , Animais , Deficiência de Colina/metabolismo , Regulação para Baixo , Feminino , Metionina/deficiência , Biossíntese de Proteínas , Proteômica , RNA Mensageiro/genética , Ratos , Triglicerídeos/metabolismo , Regulação para Cima , Aumento de Peso
14.
Br J Nutr ; 97(6): 1090-8, 2007 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-17433124

RESUMO

The methionine cycle and methyl group metabolism are implicated in the long-term programming of metabolism. Diets deficient in folic acid, methionine and choline have been fed to pregnant rats to examine the effects on amino acid metabolism, choline reserves and DNA methylation in dam and fetuses. Animals were fed folate-deficient, folate-deficient with low methionine, folate-deficient with low choline and folate-deficient, low-methionine, low-choline diets starting 2 weeks before mating. The dams and their fetuses were subsequently killed on day 21 of gestation for analysis. Diets low in methionine reduced fetal and maternal weight. Folate deficiency increased the concentrations of homocysteine, glycine, serine and threonine in the maternal plasma, and this was exacerbated by the low-methionine diets. The changes in the amino acid profile in the fetal serum were similar but less pronounced. This result suggests that fetal metabolism was less perturbed. Folate deficiency increased free choline in the maternal liver at the expense of phosphocholine stores. It has been suggested that a deficiency in methyl donors in the diet during pregnancy may impact on key methylation reactions, including the methylation of DNA. Despite widespread changes in the metabolism of choline and amino acids, there was no change in the global methylation of cytosine in DNA from either maternal or fetal livers. This suggests a more indirect mechanism in which gene-nutrient interactions modify the process of differential methylation during development.


Assuntos
Metilação de DNA , Feto/metabolismo , Deficiência de Ácido Fólico/metabolismo , Complicações na Gravidez/metabolismo , Aminoácidos/sangue , Animais , Colina/metabolismo , Dieta , Feminino , Ácido Fólico/metabolismo , Fígado/embriologia , Fígado/metabolismo , Troca Materno-Fetal/fisiologia , Redes e Vias Metabólicas/fisiologia , Metionina/metabolismo , Fosforilcolina/metabolismo , Gravidez , Ratos , Aumento de Peso
15.
Br J Nutr ; 97(5): 912-20, 2007 May.
Artigo em Inglês | MEDLINE | ID: mdl-17408526

RESUMO

The available evidence suggests that metabolic control mechanisms are programmed early in life. Previous studies of pregnant rats fed low-protein diets have suggested that the vegetable oils used in the experimental diets influence the outcome. The present study investigated the offspring of female rats fed semi-synthetic diets containing either 180 or 90g casein/kg with 70 g/kg (w/w) of either corn oil or soya oil during gestation. During lactation, the dams received stock diet, and the offspring were subsequently weaned onto the stock diet. The offspring of dams fed the low-protein diets were smaller at birth. At 25 weeks of age, the offspring were subjected to an oral glucose tolerance test. In the offspring of dams fed the diet containing soya oil, the area under the insulin curve was affected by the protein content of the maternal diet. There was no effect of protein on the area under the insulin curve in the offspring of dams fed the diet prepared with corn oil. There were no differences in plasma glucose concentrations. The levels of mRNA for acetyl-CoA carboxylase- in the livers of female offspring were affected by the protein and oil content of the maternal diet. The level of carnitine palmitoyl transferase mRNA was affected by the protein content of the maternal diet. The present study suggests that PUFA in the maternal diet can interact with protein metabolism to influence the development of the offspring. This may involve the higher content of alpha-linolenic acid in soya oil compared with corn oil.


Assuntos
Dieta com Restrição de Proteínas/métodos , Gorduras Insaturadas na Dieta/metabolismo , Proteínas Alimentares/metabolismo , Insulina/sangue , Óleos de Plantas/metabolismo , Acetil-CoA Carboxilase/genética , Aminoácidos/análise , Animais , Peso Corporal/fisiologia , Carnitina O-Palmitoiltransferase/genética , Óleo de Milho/administração & dosagem , Óleo de Milho/metabolismo , Gorduras Insaturadas na Dieta/administração & dosagem , Proteínas Alimentares/administração & dosagem , Ingestão de Alimentos/fisiologia , Feminino , Expressão Gênica/genética , Teste de Tolerância a Glucose , Hematócrito , Resistência à Insulina/fisiologia , Masculino , Troca Materno-Fetal/fisiologia , Tamanho do Órgão/fisiologia , Óleos de Plantas/administração & dosagem , Gravidez , Ratos , Ratos Endogâmicos , Fatores Sexuais , Óleo de Soja/administração & dosagem , Óleo de Soja/metabolismo
16.
Reprod Nutr Dev ; 46(3): 227-39, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-16733043

RESUMO

To characterise the effects of dietary protein content on threonine metabolism during pregnancy, rats were fed diets containing 18% or 9% protein and then killed at different stages of gestation. Serum threonine concentrations fell significantly faster in the animals fed the diet containing 9% protein when compared to those fed the diet containing 18% protein. On day 4 of gestation the rate of threonine oxidation was higher in maternal liver homogenates prepared from the animals fed the diet containing 18% protein. The rate of threonine oxidation by liver homogenates fell as gestation proceeded in both diet groups. The activity of threonine dehydrogenase in the maternal liver was unaffected by dietary protein content at all stages of gestation. Serine-threonine dehydratase activity in homogenates of the maternal liver was transiently increased during the early stages of gestation in the animals fed high protein diets but was unchanged in the low protein groups. There was an increase in serine-threonine dehydratase activity in the kidney during the later stages of gestation but this was unaffected by the protein content of the maternal diet. These data show that the changes in free threonine concentrations cannot be accounted for through changes in the oxidation rate and suggest that some other factor influences the unusual metabolism of this amino acid during gestation.


Assuntos
Aminoácidos/metabolismo , Proteínas Alimentares/administração & dosagem , Prenhez/metabolismo , Treonina/metabolismo , Oxirredutases do Álcool/metabolismo , Animais , Relação Dose-Resposta a Droga , Feminino , Idade Gestacional , Rim/enzimologia , Rim/metabolismo , L-Serina Desidratase/metabolismo , Fígado/enzimologia , Fígado/metabolismo , Oxirredução , Gravidez , Distribuição Aleatória , Ratos , Ratos Endogâmicos , Treonina/sangue
17.
Br J Nutr ; 94(1): 12-8, 2005 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-16115327

RESUMO

During fetal life, there are periods of rapid cell proliferation, which are uniquely sensitive to nutritional perturbation. Feeding the pregnant rat a protein-restricted diet alters the growth trajectory of major fetal organs such as the kidney. By day 21 of gestation, the ratio of kidney weight to total body weight is reduced in the fetuses of dams fed a protein-deficient diet. In contrast, the ratio of fetal liver weight to total body weight is unchanged. To investigate the mechanisms underlying this disproportionate change in organ growth in the low-protein group, cell proliferation and differentiation have been assessed in the liver and kidney. The steady-state levels of mRNA for the growth-arrest and DNA-damage gene gadd153/CHOP-10, CCAAT enhancer-binding proteins alpha and beta were unaffected by maternal diet in both fetal liver and kidney. The mRNA for alpha-fetoprotein, albumin and hepatic glucokinase were unchanged in the liver, suggesting that maternal protein deficiency does not alter the state of differentiation. The steady-state levels of the mRNA coding for the cyclin-dependent protein kinase inhibitors (p15(INK4a), p19(INK4d), p21(CIP1), p27(KIP1) and p57(KIP2)) were unchanged in the fetal livers but were significantly increased in the kidneys of fetuses from dams fed the low-protein diet. These results show that the asymmetrical growth of the kidney is associated with increases in mRNA for the Cip/Kip cyclin-dependent kinase inhibitors and that these may reflect specific lesions in organ development.


Assuntos
Dieta com Restrição de Proteínas/métodos , Expressão Gênica/genética , Rim/embriologia , Fígado/embriologia , Animais , Peso Corporal/genética , Proteínas Estimuladoras de Ligação a CCAAT/genética , Diferenciação Celular/genética , Divisão Celular/genética , Quinases Ciclina-Dependentes/antagonistas & inibidores , Quinases Ciclina-Dependentes/genética , Dano ao DNA/genética , Feminino , Genes cdc/fisiologia , Masculino , Tamanho do Órgão , Gravidez , RNA Mensageiro/análise , Ratos , Ratos Endogâmicos , Fator de Transcrição CHOP , Fatores de Transcrição/genética , alfa-Fetoproteínas/genética
18.
J Nutr ; 132(8): 2137-42, 2002 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-12163652

RESUMO

The flow of amino acids to both protein and DNA synthesis is particularly important during periods of rapid cell proliferation such as the fetal stages of life. The changes in mRNA levels caused by the different types of growth arrest were studied in F9 embryonal carcinoma cells. The cells were grown in medium deficient in the amino acid lysine or in one containing phosphonoacetyl L-aspartic acid (PALA), which inhibits the incorporation of aspartic acid into pyrimidine nucleotides. A number of mRNAs known to be elevated in growth arrested cells (gas and gadd) were studied by Northern blotting. Samples of RNA from the cells were also compared by differential display reverse transcription-polymerase chain reaction (DDRT-PCR). The results showed that lysine deficiency increased the steady-state levels of a number of mRNAs by 5- to 40-fold. In contrast, the changes in cells treated with PALA were much smaller and less pronounced. Amino acid deficiency induced the mRNAs coding for gadd153 (CHOP-10), gas5, the mouse doublesex-related gene (Dmrt1) and the polyamine modulated factor (PA-1) as well as a number of unidentified expressed sequence tags (EST). These mRNAs were all induced within 24 h of exposure to amino acid deficiency. These very different transcriptional responses may be important in understanding the interactions between protein quantity and quality in different physiologic situations.


Assuntos
Aminoácidos/deficiência , Perfilação da Expressão Gênica , Regulação da Expressão Gênica , Animais , Sequência de Bases , Carcinoma Embrionário , Camundongos , Camundongos Endogâmicos C57BL , RNA Mensageiro/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Células Tumorais Cultivadas
19.
J Nutr ; 134(6): 1493-9, 2004 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-15173417

RESUMO

Poor development in utero may favor the development of obesity in adulthood. Animal studies showed that embryo manipulation in vitro or nutritional insults during the embryonic and fetal stages of development may lead to obesity in adult life. We studied the in vitro proliferation and differentiation of adipocytes to investigate whether early protein restriction may program cell growth and development. In a series of experiments, 2 different low-protein diet protocols were compared. In both cases, pregnant rats were fed a diet with a high (18-20%) or low (8-9%) protein content during gestation and/or lactation. Preadipocytes were isolated from the fetuses, neonates, and weanling offspring. Moderate protein restriction, imposed during either gestation and/or lactation, did not affect the capacity of preadipose cells to divide or store fat. Because previous studies showed that early protein restriction alters the metabolism of sulfur amino acids, we also investigated the effects of methionine, taurine, and homocysteine on proliferation and differentiation of preadipocytes. The supplementation of the diet with methionine or the addition of homocysteine and taurine to the culture media did not influence the development of preadipocytes. We obtained no evidence for the direct reprogramming of the precursor or stem cells and suggest that the subsequent alteration in fat accretion may therefore reflect a change in the neuroendocrine environment.


Assuntos
Adipócitos/citologia , Dieta com Restrição de Proteínas , Prenhez , Células-Tronco/citologia , Animais , Animais Recém-Nascidos/crescimento & desenvolvimento , Vasos Sanguíneos/citologia , Vasos Sanguíneos/embriologia , Diferenciação Celular , Divisão Celular , Células Cultivadas , Meios de Cultura , Epididimo/citologia , Feminino , Feto/citologia , Homocisteína/administração & dosagem , Rim/citologia , Lactação , Masculino , Metionina/administração & dosagem , Gravidez , Ratos , Ratos Endogâmicos , Células Estromais/citologia , Tela Subcutânea/irrigação sanguínea , Tela Subcutânea/embriologia , Taurina/administração & dosagem , Desmame
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