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CystinuriaCleland, Joan Burton. January 1947 (has links) (PDF)
Typewritten copy Includes bibliographical references.
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Maternal green tea epigallocatechin gallate supplementation counteracts high-fat diet-induced metabolic derangements in dams andtheir male offspring: a programming effectLi, Shiying, 李诗盈 January 2012 (has links)
The overall objective of this thesis was to test the hypothesis that through developmental programming maternal overnutrition-induced metabolic derangements in the offspring could be offset by supplementing the maternal diet with green tea epigallocatechin gallate (GTEG).
The obesogenic diet was a high-fat (HF, 30%) diet. Female Sprague-Dawley rats were fed the HF, low-fat (LF, 7%) or HF diet containing 0.75% or 1.0% GTEG (GT1, GT2) from before conception and throughout gestation and lactation. Both doses of GTEG significantly improved metabolic control of the HF-fed lactating dams. The weaned male pups received the HF, GT1 or GT2 diet forming 6 dam/pup groups: LF/HF, HF/HF, HF/GT1, HF/GT2, GT1/HF and GT2/HF. At wk 13 they had similar weight but insulin resistance index (IRI), serum non-esterified fatty acid (NEFA) and liver triglyceride of rats born to GTEG dams was 57, 23 and 26% lower and accompanied by improved gene/protein expressions related to lipid and glucose metabolism compared to HF/HF rats (P < 0.05). Although the HF/GT1 and HF/GT2 rats had lower serum NEFA, their serum insulin and IRI remained comparable with the HF/HF rats.
To determine if there is a critical time period for the actions of GTEG, in the second experiment female rats were fed the LF, HF, or GT1 diet prior to conception and throughout gestation. During lactation, half of the dams had their diet switched from HF to GT1 and vice versa. Pups were weaned to the HF or LF diet, forming the LF/LF/LF, LF/LF/HF, HF/HF/LF, HF/HF/HF, HF/GT1/LF, HF/GT1/HF, GT1/GT1/LF, GT1/GT1/HF, GT1/HF/LF and GT1/HF/HF groups. Metabolic controls of dams given GT1 during gestation or lactation were improved compared with the HF/HF dams (P < 0.05). Three-way ANOVA revealed that 22 wk old offspring born to dams fed the HF diet during gestation had higher serum and muscle triglyceride (TG) concentration and lower ferric reducing ability of plasma (FRAP) (P < 0.05), all of which were reversed by supplementing GT1 to the gestational diet. Oral glucose tolerance at wk 15 was improved in those offspring born to dams given GT1 supplementation during lactation (P < 0.05). The increased serum NEFA concentration and IRI in offspring of dams fed the HF diet during gestation or lactation were reversible upon GT1 supplementation during either time period (P < 0.05). These rats (HF/GT1/HF, GT1/GT1/HF and GT1/HF/HF) had similar level of hepatic insulin receptor gene expression as well as protein abundance for muscle glucose transporter 4 and hepatic sterol regulatory element binding protein-1c but lower protein mass for hepatic glucose-6-phosphatase (P < 0.05) compared with the LF/LF/HF rats.
Hence, maternal overnutrition-induced metabolic derangements in male offspring are reversible through supplementing GTEG to the maternal diet during gestation or lactation and this approach is more effective than giving GTEG to offspring born to overnourished mothers. Offspring metabolism could be programmed via manipulations of the maternal diet. / published_or_final_version / Biological Sciences / Doctoral / Doctor of Philosophy
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Maternal bitter melon supplementation reduces the risk for metabolic defects later in life: effects on lipidhandling, oxidative stress and inflammation in offspring born to damsfed a high fructose dietChing, Hiu-ha., 程曉霞. January 2012 (has links)
The relationship between fructose consumption and metabolic
diseases has drawn substantial attention in recent years. Dietary fructose
consumption has climbed dramatically in the past 40 years, and this trend
coincides with the prevalence of obesity and diabetes worldwide. In
rodents, maternal obesogenic diets are associated with higher risks of
metabolic derangement later in life whereas bitter melon (BM)
supplementation has been shown to improve blood glucose and lipid
profiles. The overall objective of this thesis was to test the hypothesis that
through developmental programming metabolic derangement in offspring
born to rat dams fed a high-fructose (F) diet could be offset by the addition
of BM to the maternal diet.
Virgin female rats received a control (C), F (60%) or BM-supplemented
F (FBM,1%) diet 8 weeks before conception and throughout gestation and
lactation. Weaned male offspring consumed C diet (C/C,F/C,FBM/C) for 11
weeks. The concentrations of serum insulin, triglyceride, free fatty acid
(FFA), and hepatic lipids in FBM/C offspring matched that in C/C offspring
and were significantly lower than F/C offspring. These phenotypic changes
were accompanied with suppressed hepatic lipogenic gene expression but
enhanced expression of lipid oxidation-related genes.
In the second experiment, we extended the earlier findings by
examining whether adding BM to F-fed dams would still benefit offspring if
they continued to consume the F diet postweaning. This simulates the
scenario in affluent societies where fructose overconsumption may occur in
two consecutive generations. The dose-response effect of BM at doses of
0.85% (FBM1) and 1% (FBM2) was also examined. Male offspring born to
dams fed the C, F, FBM1 or FBM2 diet were weaned to C or F diet
(C/C,C/F,F/F,FBM1/F,FBM2/F) for 20 weeks. BM normalized the serum
FFA elevation observed in F/F offspring, although hyperinsulinemia
remained in FBM1/F and FBM2/F offspring. The altered liver lipid profile
and its molecular changes observed in F/F offspring were ameliorated by
maternal BM supplementation. Lower adipose expression of
mesoderm-specific transcript, hormone sensitive lipase, sterol regulatory
element-binding transcription factor 1, and peroxisome
proliferator-activated receptor-gamma (PPARγ) and PPARγ-target genes in
FBM1/F and FBM2/F offspring indicated that BM could reduce adipocyte
size as well as lower lipolysis and lipogenesis.
Since FFA stimulates reactive oxygen species generation that
enhances cellular stress, oxidative stress and inflammation in offspring of
two-generation F exposure with or without maternal BM supplementation
were examined. FBM1/F and FBM2/F offspring showed reduced lipid
peroxidation but enhanced antioxidant capacity in the liver. BM suppressed
the expression of proinflammatory genes and phosphorylation of c-Jun
amino terminal kinase1, as well as promoted insulin receptor substrate 1
protein expression. These BM-mediated antioxidant and anti-inflammatory
effects may be associated with a reduction of circulating FFA.
Taken together, the data support the concept of developmental
programming as maternal fructose clearly induced dyslipidemia, adipocyte
dysfunction, oxidative stress and inflammation in offspring. That these
abnormalities were largely reversed by adding BM to the maternal diet
suggests that perinatal BFC supplementation could alter the course of
maternal malnutrition-induced metabolic defects later in life. / published_or_final_version / Biological Sciences / Doctoral / Doctor of Philosophy
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Perinatal sulfur amino acid toxicity.Knipfel, J. E. January 1973 (has links)
No description available.
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Cross-correctional studies in inborn errors of vitamin B12 metabolismByck, Susan January 1989 (has links)
Human skin fibroblasts derived from patients with all 7 known inborn errors of vitamin B$ sb{12}$ metabolism have been studied for functional integrity of methylmalonyl CoA mutase and methionine synthase. Cocultivation of cblC and cblF fibroblasts in the absence of polyethylene glycol resulted in a twofold increase over the expected in both ($ sp{14}$C) propionate and ($ sp{14}$C) methyltetrahydrofolate incorporation into acid-precipitable material, suggesting that metabolic cooperation between cells occurs. CblD fibroblasts, which are biochemically similar to cblC cells (Goodman et al, 1970; Willard et al, 1977), do not cooperate metabolically when mixed with cblF cells. Partial correction in phenotype was seen in mixtures of cblD and cblG cells, but not cblC and cblG cells. These observations lend further support for the division of cblC and cblD disease into two discrete complementation classes. Cocultivation of cblF fibroblasts with both cblE and cblG cells also resulted in partial correction in phenotype. / ($ sp{14}$C) Propionate incorporation in both cblC and cblF cells exposed to conditioned medium from control cells was increased more than twofold. ($ sp{14}$C) methyltetrahydrofolate incorporation in cblC cells exposed to conditioned medium from cblF cells was increased twofold. This suggests the presence of a diffusible factor correcting the defect in the mutant cell lines.
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Isolation of human BCAD gene and analysis of putative BCAD deficiencyFu, Katherine January 1993 (has links)
The 2-methylbranched chain acyl-CoA dehydrogenase (BCAD) is a mitochondrial enzyme that catalyzes the third reaction in isoleucine and valine metabolism, the oxidation of 2-methylbutyryl-CoA and isobutyryl-CoA, respectively. BCAD deficiency would result in the accumulation of branched chain acyl-CoAs or their derivatives. Three patients with a putative defect in BCAD have been reported. This study consists of a molecular examination of one such patient as well as the characterization of the BCAD gene. In Northern blot analysis of human fibroblast RNA, the BCAD cDNA hybridized to two RNA species of 2.7 and 6.5 kb. The 2.7 kb band corresponds to the size of the BCAD cDNA, which consists of the entire coding region of 1.3 kb and a 3$ sp prime$ untranslated region of 1.4 kb. The coding regions of the BCAD gene span approximately 21 kb and consist of 12 exons and 11 introns. The exons range in size from 39 to 108 bp. In the analysis of the putative BCAD-deficient patient, no significant difference was observed at the level of DNA (Southern), RNA (Northern) or protein (Western) when compared to controls, suggesting that the BCAD gene in this patient did not contain any large insertions or deletions, or a frameshift mutation. The single strand conformation polymorphism (SSCP) technique and sequencing of the entire coding region did not reveal any disease-causing mutations but two polymorphisms were identified: one in exon 6 and the other in exon 10.
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Intragenic complementation in methylmalonyl CoA mutaseFarah, Rita S. January 1994 (has links)
Methylmalonic aciduria (MMA) is an autosomal recessive metabolic disorder with an incidence of 1 in 48,000, which may be due to a defect in the mitochondrial homodimeric enzyme methylmalonyl CoA mutase (mut MMA). mut MMA is subdivided into $mut sp circ$ and $mut sp-$ subclasses on the basis of complementation analysis; $mut sp circ$ cell lines have very low incorporation of ($ sp{14}$C) from propionate into acid precipitable material while incorporation in $mut sp-$ cells is increased when cells are incubated in cobalamin. Intragenic complementation was first observed with WG 1130, a $mut sp circ$ fibroblast line with a homozygous R93H mutation, that is capable of complementing MCM activity when fused with some $mut sp circ$ and some $mut sp-$ cells (1). Extensive intragenic complementation in mut MMA was subsequently observed. Fibroblasts cultured from thirteen unrelated patients (6 $mut sp-$, 7 $mut sp circ$) were fused in all possible pairwise combination and MCM activity was assayed in the heterokaryons by measuring the incorporation of ($ sp{14}$C) from propionate into acid precipitable material. Intragenic complementation, indicated by stimulation of ($ sp{14}$C) -propionate incorporation following cell fusion with polyethylene glycol, was observed in fusions involving twelve of the thirteen strains. Of these thirteen strains, mutations have been identified in six; four have a homozygous mutation (WG 1130 (R93H), WG 1511 (H678R), WG 1610 (G717V), WG 1609 (G630E)), and two cell lines are compound heterozygous (WG 1681 (G623R and G703R), WG 1607 (W105R and A377E)); the remainders are yet to be determined. These intragenic complementations will provide information for grouping the mutations in defined domains in order to correlate structure and function of MCM.
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The molecular characterization of mutations at the methylmalonyl CoA mutase locus involved in interallelic complementation /Qureshi, Amber A. (Amber Ateef) January 1993 (has links)
Methylmalonic aciduria is an autosomal recessive metabolic disorder, which may be due to a defect in the methylmalonyl CoA mutase (MCM) apoenzyme. The mut$ sp circ$ mutation is characterized by undetectable enzyme activity in cell extracts, and by the low incorporation of ($ sp{14}$C) propionate in the presence of hydroxocobalamin in culture. A mut$ sp circ$ fibroblast cell line, WG 1681, from an African-American male infant was shown to complement another mut$ sp circ$ cell line, WG 1130. Subsequent cloning and sequencing of cDNA from WG 1681 identified two previously described homozygous polymorphisms: H532R and V671I(1). In addition, compound heterozygosity was observed for two novel changes at highly conserved sites: G623R and G703R. Hybridization of allele specific oligonucleotides to PCR amplified MCM exons from WG 1681 and family members identified a clinically normal mother, sister and half-brother as carriers of the G703R change in cis with both polymorphisms. The putative father was not identified as a carrier of the G623R change. transfection of each change, singly and in cis with both polymorphisms, into GM1673 cells demonstrated a lack of stimulation of ($ sp{14}$C) propionate uptake in the absence and presence of OH-Cbl, in comparison to controls. Co-transfection of each separate mutation with the previously identified R93H mutation of WG 1130 (2) stimulated propionate uptake. These results indicate that G623R and G703R are novel mutations responsible for deficient MCM activity and the mut$ sp circ$ phenotype in WG 1681, and both mutations are independently capable of complementing the R93H mutation of WG 1130.
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A "new" disorder of isoleucine catabolism /Daum, Robert S. January 1973 (has links)
No description available.
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Relationship between Emotional Competence and Metabolic Control in Adolescents with Insulin Dependent Diabetes Mellitus (IDDM)Nesin, April Erwin January 2004 (has links) (PDF)
No description available.
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