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1.
Am J Physiol Endocrinol Metab ; 320(3): E438-E452, 2021 03 01.
Article in English | MEDLINE | ID: mdl-33427054

ABSTRACT

Obesity is a prevailing problem across the globe. Women who are obese have difficulty initiating and sustaining lactation. However, the impact of genetics and diet on breastfeeding outcomes is understudied. Here we explore the effect of diet and genotype on lactation. We utilized the low-density lipoprotein receptor (Ldlr-KO) transgenic mouse model as an obesity and hypercholesterolemia model. Additionally, we used the tryptophan hydroxylase 1 (Tph1-KO) mouse, recently identified as a potential anti-obesogenic model, to investigate if addition of Tph1-KO could ameliorate negative effects of obesity in Ldlr-KO mice. We created a novel transgenic mouse line by combining the Ldlr and Tph1 [double knockout (DKO)] mice to study the interaction between the two genotypes. Female mice were fed a low-fat diet (LFD; 10% fat) or high-fat diet (HFD; 60% fat) from 3 wk of age through early [lactation day 3 (L3)] or peak lactation [lactation day 11 (L11)]. After 4 wk of consuming either LFD or HFD, female mice were bred. On L2 and L10, dams were milked to investigate the effect of diet and genotype on milk composition. Dams were euthanized on L3 or L11. There was no impact of diet or genotype on milk protein or triglycerides (TGs) on L2; however, by L10, Ldlr-KO and DKO dams had increased TG levels in milk. RNA-sequencing of L11 mammary glands demonstrated Ldlr-KO dams fed HFD displayed enrichment of genes involved in immune system pathways. Interestingly, the DKO may alter vesicle budding and biogenesis during lactation. We also quantified macrophages by immunostaining for F4/80+ cells at L3 and L11. Diet played a significant role on L3 (P = 0.013), but genotype played a role at L11 (P < 0.0001) on numbers of F4/80+ cells. Thus the impact of diet and genotype on lactation differs depending on stage of lactation, illustrating complexities of understanding the intersection of these parameters.NEW & NOTEWORTHY We have created a novel mouse model that is focused on understanding the intersection of diet and genotype on mammary gland function during lactation.


Subject(s)
Diet, High-Fat , Lactation , Mammary Glands, Animal/metabolism , Receptors, LDL/genetics , Tryptophan Hydroxylase/genetics , Animals , Dietary Fats/pharmacology , Female , Gene-Environment Interaction , Genotype , Lactation/drug effects , Lactation/genetics , Mammary Glands, Animal/drug effects , Maternal Nutritional Physiological Phenomena/drug effects , Maternal Nutritional Physiological Phenomena/genetics , Mice , Mice, Knockout , Mice, Obese , Obesity/genetics , Obesity/metabolism
2.
Curr HIV/AIDS Rep ; 17(4): 269-280, 2020 08.
Article in English | MEDLINE | ID: mdl-32507984

ABSTRACT

PURPOSE OF REVIEW: The purpose of this review is to describe and assess the literature on mobile health (mHealth) and other technology-based HIV testing interventions published in the 5-year period from 2015 to 2020. RECENT FINDINGS: We identified 18 published technology-based studies, 6 of which were efficacy trials and the remaining 12 were either pilot randomized controlled trials (RCTs) or quasi-experimental studies. Most (n = 10) interventions were conducted outside the USA, including countries in Sub-Saharan Africa (n = 4), China (n = 3), Latin America (n = 2), and India (n = 1). All efficacy trials showed some evidence of efficacy, although uptake of HIV testing was low among in intervention trials that consisted of a low number of text messages. Most pilot RCTs demonstrated high levels of feasibility and acceptability, as well as some evidence that the intervention participants benefited more than the control group. Many non-randomized trials similarly reported positive appraisal by study participants. Recommendations for future research and practice by the authors of the studies reviewed here are summarized. Technology-assisted HIV testing interventions may be an important strategy to reach national and global targets for HIV status awareness in the general population and for most at-risk groups. Although there appears to be growing evidence of their benefit, questions linger regarding how to leverage existing social media platforms to promote HIV testing, which interventions work for what populations, and best practices for scaling up mHealth and other technology-based interventions.


Subject(s)
Computers, Handheld/statistics & numerical data , HIV Infections/diagnosis , Mass Screening/methods , Smartphone/statistics & numerical data , Telemedicine/methods , China , Humans , Text Messaging
3.
J Assoc Nurses AIDS Care ; 31(3): 279-289, 2020.
Article in English | MEDLINE | ID: mdl-31436599

ABSTRACT

Half of the people living with HIV have cognitive deficits indicative of HIV-associated neurocognitive disorders (HANDs). With few treatment options, informing patients about a HAND diagnosis is a questionable practice. A sample of 139 people living with HIV were administered gold-standard cognitive tests; scores were used to determine whether they met cognitive criteria for HAND. Participants were informed that they met the criteria for HAND and asked 2 open-ended questions about their reactions to learning this information. Participant responses were recorded verbatim and coded into 3 overarching themes: positive, indifferent, and negative. Positive responses contained subthemes of confirmation, gratitude, desire for improvement, and curiosity. Indifferent responses contained nonreactive responses, apathy, and confusion. Negative responses contained surprise, discontentment, fear, and denial. Although most participants responded positively to feedback about HANDs, others experienced distress. Nurse clinicians should be mindful about informing patients if they have HAND while also educating them about brain health.


Subject(s)
Cognitive Dysfunction/psychology , HIV Infections/complications , Neurocognitive Disorders/epidemiology , Neurocognitive Disorders/psychology , Adult , Aged , Cognition/physiology , Cognition Disorders/psychology , Cognitive Dysfunction/epidemiology , Cognitive Dysfunction/etiology , Cognitive Reserve , Female , HIV Infections/epidemiology , HIV Infections/psychology , Humans , Male , Middle Aged , Neurocognitive Disorders/complications , Neurocognitive Disorders/diagnosis , Neuronal Plasticity
4.
J Psychosoc Nurs Ment Health Serv ; 57(12): 48-55, 2019 Dec 01.
Article in English | MEDLINE | ID: mdl-31437282

ABSTRACT

Approximately 50% of persons with HIV (PWH) meet the cognitive criteria for HIV-associated neurocognitive disorder (HAND). Informing PWH they may have HAND raises concerns given the lack of consensus-derived treatment options and overall knowledge about HAND. Thus, the current qualitative descriptive study aimed to describe PWHs' reactions to a possible diagnosis of HAND. Cognitive tests were administered to 135 PWH to determine whether they met the criteria for HAND. From 135 PWH, 109 (80.7%) participants met the cognitive criteria and were informed about their probable HAND diagnosis. Approximately 2 months later, the remaining 85 participants (24 were lost to attrition) were asked about their reactions and concerns to receiving a probable diagnosis of HAND. Their responses were thematically coded. Themes that emerged were Desire to Improve, Confirmation, Not Concerned/No Reaction, Concerned, Unexpected, Anxiety, Knowledge Seeking, and Sadness. Most themes were positive or neutral, whereas fewer negative themes were observed. Thematic/content analysis appeared to show that most PWH reacted well to their probable diagnosis and were open to ways to improve their brain health. Such openness represents a window to provide health education to patients. Implications for practice and research are provided. [Journal of Psychosocial Nursing and Mental Health Services, 57(12), 48-55.].


Subject(s)
Cognitive Dysfunction/diagnosis , HIV Infections/psychology , Neurocognitive Disorders/diagnosis , Adult , Anxiety/psychology , Female , Humans , Male , Middle Aged , Neurocognitive Disorders/psychology , Neuropsychological Tests , Qualitative Research , Surveys and Questionnaires
5.
Front Vet Sci ; 5: 247, 2018.
Article in English | MEDLINE | ID: mdl-30356776

ABSTRACT

The objective of this longitudinal cohort study was to describe the milk microbiota of dairy cow mammary glands based on inflammation status before and after the dry period. Individual mammary quarters were assigned to cohorts based on culture results and somatic cell count (SCC) at dryoff and twice in the first 2 weeks post-calving. Mammary glands that were microbiologically negative and had low SCC (< 100,000 cells/mL) at all 3 sampling periods were classified as Healthy (n = 80). Microbiologically negative mammary glands that had SCC ≥150,000 cells/mL at dryoff and the first post-calving sample were classified as Chronic Culture-Negative Inflammation (CHRON; n = 17). Quarters that did not have both culture-negative milk and SCC ≥ 150,000 cells/mL at dryoff but were culture-negative with SCC ≥ 150,000 at both post-calving sampling periods were classified as Culture-Negative New Inflammation (NEWINF; n = 6). Mammary glands with bacterial growth and SCC ≥ 150,000 cells/mL at all 3 periods were classified as Positive (POS; n = 3). Milk samples were collected from all enrolled quarters until 150 days in milk and subjected to microbiota analysis. Milk samples underwent total DNA extraction, a 40-cycle PCR to amplify the V4 region of the bacterial 16S rRNA gene, and next-generation sequencing. Healthy quarters had the lowest rate of PCR and sequencing success (53, 67, 83, and 67% for Healthy, CHRON, NEWINF, and POS, respectively). Chao richness was greatest in milk collected from Healthy quarters and Shannon diversity was greater in milk from Healthy and CHRON quarters than in milk collected from glands in the NEWINF or POS cohorts. Regardless of cohort, season was associated with both richness and diversity, but stage of lactation was not. The most prevalent OTUs included typical gut- and skin-associated bacteria such as those in the phylum Bacteroidetes and the genera Enhydrobacter and Corynebacterium. The increased sequencing success in quarters with worse health outcomes, combined with the lack of bacterial growth in most samples and the high PCR cycle number required for amplification of bacterial DNA, suggests that the milk microbiota of culture-negative, healthy mammary glands is less abundant than that of culture-negative glands with a history of inflammation.

6.
Psychosomatics ; 57(1): 25-30, 2016.
Article in English | MEDLINE | ID: mdl-26791513

ABSTRACT

BACKGROUND: Although the first medically-reported case of auto-enucleation was described in the mid-19th century, ocular self-gouging has long been depicted in historical legend and mythology. Cases of enucleation have since been identified across various cultures. Though relatively uncommon, this major form of self-mutilation now afflicts approximately 500 individuals per year, and may present more commonly among certain clinical populations. METHODS: We present 2 cases of self-enucleation in patients with psychotic illnesses and review existing literature on the history of enucleation, associated pathology, and management (both medically and psychiatrically) for this serious form of self-injury. RESULTS: Literature review includes a brief historical perspective of auto-enucleation and its context in psychosomatic medicine, with cases to highlight key aspects in the prevention and management of ocular self-injury. Normal eye pathology is described briefly, with a focus on medical care after self-inflicted damage, as pertinent to consultation psychiatrists. Interventions for behavioral and pharmacologic management of agitation and impulsivity are reviewed, including consideration for electroconvulsive therapy, in this particular context. CONCLUSION: Although severe ocular self-injury is uncommon, psychiatrists should be familiar with approaches to prevent and manage auto-enucleation in individuals at risk thereof. Consultation psychiatrists must work closely with ophthalmologists to address affective, behavioral, and cognitive triggers and complications of ocular self-injury.


Subject(s)
Antipsychotic Agents/therapeutic use , Eye Injuries/surgery , Psychotic Disorders/psychology , Schizophrenia/therapy , Schizophrenic Psychology , Self Mutilation/psychology , Adult , Electroconvulsive Therapy/adverse effects , Humans , Intraocular Pressure , Male , Middle Aged , Ocular Hypertension/etiology , Ophthalmologic Surgical Procedures , Psychotic Disorders/therapy , Self Mutilation/therapy
7.
Mol Cell Proteomics ; 12(1): 194-206, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23105009

ABSTRACT

Changes in the actin cytoskeleton, especially the formation of cross-linked actin networks (CLANs) are thought to contribute to the increased intraocular pressure observed in primary open-angle and steroid-induced glaucoma. To better understand the effects of glucocorticoids, we employed a shotgun method to analyze global changes in the cytoskeleton and integrin signaling pathways following dexamethasone (DEX) treatment of human trabecular meshwork (HTM) cells. RNA and cell lysates were obtained from HTM cells incubated with or without DEX. Changes in protein expression were determined by mass spectrometry (MS) following differential centrifugation of cell lysates to enrich for low-abundance cytoskeletal and signaling proteins, proteolytic digestion, and a titanium dioxide column to enrich for phosphopeptides. Results were validated by Western blots. Changes in RNA levels were determined with gene arrays and RT-PCR. Overall, MS identified 318 cytoskeleton associated proteins. Five of these proteins (PDLIM1, FGFR1OP, leiomodin-1, ZO-2 and LRP16A) were only detected in DEX-treated cells by MS. However, only PDLIM1 showed a statistically significant increase at the RNA level. Other proteins with differences at both the RNA and protein levels included ß3 integrin, caveolin-1, Borg2, raftlin1, PI-3 kinase regulatory subunit α, transgelin, and filamin B. By immunofluorescence microscopy filamin B and PDLIM1 showed enhanced expression in human trabecular meshwork cells, but only PDLIM1 demonstrated significant localization within CLANs. Finally, MS showed that some of the cytoskeleton proteins (Borg2, leiomodin-1, LRP16A, raftlin1 and CKAP4) contained phosphorylated residues. This study suggests that DEX affects the expression of cytoskeleton proteins at the transcriptional and translational level and shows that a combined genomic and proteomic approach can be used for rapid analysis of proteins in the TM. It also shows that DEX altered the expression of components (PDLIM1 and ß3 integrins) involved in CLAN formation and provides new findings into the effects of glucocorticoids on the cytoskeleton.


Subject(s)
Actin Cytoskeleton/drug effects , Cytoskeletal Proteins/metabolism , Dexamethasone/pharmacology , Proteome/analysis , Trabecular Meshwork/drug effects , Trabecular Meshwork/metabolism , Actin Cytoskeleton/genetics , Actin Cytoskeleton/metabolism , Adult , Cells, Cultured , Gene Expression , Gene Expression Profiling , Glaucoma/etiology , Glaucoma/metabolism , Glucocorticoids/pharmacology , Humans , Integrins/metabolism , Mass Spectrometry , Phosphopeptides , Proteomics , RNA/analysis , Signal Transduction , Trabecular Meshwork/ultrastructure
8.
J Pediatr Hematol Oncol ; 31(5): 309-12, 2009 May.
Article in English | MEDLINE | ID: mdl-19415007

ABSTRACT

Hepatic iron overload is a serious complication of chronic transfusion therapy in patients with sickle cell disease (SCD). No firm consensus has been reached with regard to correlation between hepatic iron content (HIC) and variables including age, number of transfusions, and serum iron makers. Also, the role of HIC in determining hepatic injury is not well established. There is scarcity of data on chronically transfused children with SCD and no other confounding liver pathology. We aimed to further explore relationships between these variables in a cohort of children with SCD on chronic transfusion therapy naive to chelation. Liver biopsies obtained before starting chelation therapy from 27 children with sickle cell anemia receiving chronic transfusion therapy were evaluated for histologic scoring and determination of HIC. Average serum ferritin and iron saturation values were determined for 6 months before biopsy. Duration and total volume of transfusion were obtained from the medical records. All children were negative for human immunodeficiency virus, hepatitis B virus, and hepatitis C virus infections. Mean age at biopsy was 10.95+/-3.34 years. Mean duration and total volume of transfusions were 50.0+/-26.6 months and 17.4+/-9.6 L, respectively. Pearson product-moment bivariate correlation coefficients indicated significant correlations between HIC and histologic iron score, serum ferritin, iron saturation, age, and transfusion volume. After adjusting for transfusion volume, a significant correlation was only seen between HIC and transfusion volume. Mean HIC was 21.8+/-10.4 mg/g dry weight, with fibrosis observed in 10 patients and lobular inflammation in 9. HIC was higher in biopsies with fibrosis (28.2+/-3.8 mg/g) than biopsies without fibrosis (17.6+/-18.3 mg/g; P=0.012). HIC did not differ between biopsies with lobular inflammation (25.5+/-4.0 mg/g) and biopsies without inflammation (19.9+/-2.5 mg/g; P=0.22). These findings show that transfusion volume provides more insight on hepatic iron overload than serum iron markers.


Subject(s)
Anemia, Sickle Cell/therapy , Erythrocyte Transfusion/adverse effects , Iron Overload/etiology , Iron Overload/pathology , Liver/pathology , Adolescent , Biomarkers , Biopsy , Child , Child, Preschool , Chronic Disease , Cross-Sectional Studies , Female , Hepatitis/etiology , Hepatitis/metabolism , Hepatitis/pathology , Humans , Iron/metabolism , Iron Overload/metabolism , Liver/metabolism , Liver Cirrhosis/etiology , Liver Cirrhosis/metabolism , Liver Cirrhosis/pathology , Male
9.
Biochemistry ; 43(35): 11175-86, 2004 Sep 07.
Article in English | MEDLINE | ID: mdl-15366927

ABSTRACT

Apoptosis-linked gene-2 (ALG-2) encodes a 22 kDa Ca(2+)-binding protein of the penta EF-hand family that is required for programmed cell death in response to various apoptotic agents. Here, we demonstrate that ALG-2 mRNA and protein are down-regulated in human uveal melanoma cells compared to their progenitor cells, normal melanocytes. The down regulation of ALG-2 may provide melanoma cells with a selective advantage. ALG-2 and its putative target molecule, Alix/AIP1, are localized primarily in the cytoplasm of melanocytes and melanoma cells independent of the intracellular Ca(2+) concentration or the activation of apoptosis. Cross-linking and analytical centrifugation studies support a single-species dimer conformation of ALG-2, also independent of Ca(2+) concentration. However, binding of Ca(2+) to both EF-1 and EF-3 is necessary for ALG-2 interaction with Alix/AIP1 as demonstrated using surface plasmon resonance spectroscopy. Mutations in EF-5 result in reduced target interaction without alteration in Ca(2+) affinity. The addition of N-terminal ALG-2 peptides, residues 1-22 or residues 7-17, does not alter the interaction of ALG-2 or an N-terminal deletion mutant of ALG-2 with Alix/AIP1, as might be expected from a model derived from the crystal structure of ALG-2. Fluorescence studies of ALG-2 demonstrate that an increase in surface hydrophobicity is primarily due to Ca(2+) binding to EF-3, while Ca(2+) binding to EF-1 has little effect on surface exposure of hydrophobic residues. Together, these data indicate that gross surface hydrophobicity changes are insufficient for target recognition.


Subject(s)
Apoptosis/genetics , Calcium-Binding Proteins/genetics , Calcium-Binding Proteins/metabolism , Calcium/metabolism , Carrier Proteins/metabolism , EF Hand Motifs , Melanoma/metabolism , Uveal Neoplasms/metabolism , Apoptosis Regulatory Proteins , Binding Sites/genetics , Calcium/physiology , Calcium-Binding Proteins/antagonists & inhibitors , Calcium-Binding Proteins/biosynthesis , Cell Cycle Proteins , Cell Line, Tumor , Cells, Cultured , Dimerization , Down-Regulation/genetics , EF Hand Motifs/genetics , Endosomal Sorting Complexes Required for Transport , Gene Expression Regulation, Neoplastic , Humans , Melanocytes/cytology , Melanocytes/metabolism , Melanoma/genetics , Melanoma/pathology , Mutagenesis, Site-Directed , Peptide Fragments/genetics , Peptide Fragments/metabolism , Protein Conformation , Protein Structure, Tertiary/genetics , Surface Plasmon Resonance , Uveal Neoplasms/genetics , Uveal Neoplasms/pathology
10.
Cancer Res ; 64(1): 128-34, 2004 Jan 01.
Article in English | MEDLINE | ID: mdl-14729616

ABSTRACT

Metastatic tumor cells originating from cancers of a variety of tissues such as breast, skin, and prostate may remain dormant for long periods of time. In the case of uveal melanoma, the principal malignancy of the eye, complete removal of the primary tumor by enucleation can nonetheless be followed by metastatic tumor growth in distant organs months, years, or even decades later. This suggests that tumor cells have already spread to secondary sites at the time of treatment and remain dormant as micrometastases. Identifying factors that govern long-lived survival of metastatic tumor cells is therefore key to decreasing mortality associated with this and other diseases. While investigating factors differentially expressed in melanoma cells and normal melanocytes, we identified the receptor tyrosine kinase Axl and found up-regulation of Axl in uveal melanomas and melanoma cell lines by RNase protection, Western analysis, and immunohistochemistry. Axl has been shown to mediate cell growth and survival through its ligand Gas6 in non-transformed cells. To test whether stimulation of Axl can enhance survival of uveal melanoma cells, we assessed the degree of mitogenesis and cell survival by bromodeoxyuridine incorporation and trypan blue exclusion, respectively, upon stimulation of Mel 290 uveal melanoma cells with Gas6 in vitro. We show that Gas6 mediates mitogenesis and cell survival in Mel 290 cells. We further demonstrate that these effects occur specifically through the Axl receptor by modulating the expression of Axl with an antisense construct. cDNA microarray analysis of 12,687 genes then revealed that Gas6 stimulation of Axl in Mel 290 cells results primarily in the down-regulation of Cyr61, a member of the CCN protein family involved in tumor progression. These data show that the Axl pathway mediates increased survival of uveal melanoma cells, potentially advantageous during cancer dormancy, and that Axl may function in part through regulation of Cyr61.


Subject(s)
Cell Survival/physiology , Melanoma/enzymology , Melanoma/pathology , Oncogene Proteins/genetics , Receptor Protein-Tyrosine Kinases/genetics , Uveal Neoplasms/enzymology , Uveal Neoplasms/pathology , Base Sequence , Cell Division/physiology , Cells, Cultured , DNA Primers , Gene Expression Regulation, Neoplastic , Humans , Intercellular Signaling Peptides and Proteins/genetics , Melanocytes/cytology , Polymerase Chain Reaction/methods , Proto-Oncogene Proteins , Reverse Transcriptase Polymerase Chain Reaction , Transfection , Tumor Cells, Cultured , Axl Receptor Tyrosine Kinase
11.
J Agric Food Chem ; 51(6): 1543-7, 2003 Mar 12.
Article in English | MEDLINE | ID: mdl-12617581

ABSTRACT

Red wine is composed of a complex matrix of compounds that can interfere with analysis. A high-performance liquid chromatography (HPLC) procedure was developed to efficiently analyze organic acids, sugars, glycerol, and ethanol in Cynthiana (Vitis aestivalis) wine. Standard laboratory procedures (pH, titratable acidity, and color attributes) and HPLC were found reproducible for Cynthiana wine. HPLC recovery efficiency was determined by analysis of spiked and unspiked samples (model, Cynthiana, and Syrah (Vitis vinifera) wines). Although recovery of components was greater in the model wine, recovery in Cynthiana and Syrah wine was comparable. The HPLC procedure was further compared to commercial rapid enzyme analysis tests using model, Cynthiana, and Syrah wines. HPLC analyses were more accurate than enzymatic tests for determining components in the model, Cynthiana, and Syrah wines. Considering the complexity of the wines analyzed, reproducibility and recovery of the HPLC procedure was demonstrated and showed improvement and precision when compared to existing methods.


Subject(s)
Chromatography, High Pressure Liquid/methods , Fruit/chemistry , Vitis/chemistry , Wine/analysis , Carbohydrates/analysis , Carboxylic Acids/analysis , Ethanol/analysis , Glycerol/analysis , Reproducibility of Results , Sensitivity and Specificity
12.
Arch Ophthalmol ; 120(12): 1719-25, 2002 Dec.
Article in English | MEDLINE | ID: mdl-12470148

ABSTRACT

OBJECTIVE: To study the expression of angiogenic factors Cyr61 and tissue factor (TF) in uveal melanoma and its correlation with blood vessel density. METHODS: Suppression subtractive hybridization was used to identify genes that are differentially expressed between cell lines of uveal melanoma and normal uveal melanocytes. Expression of these genes was subsequently verified in primary uveal melanomas and correlated with the number of blood vessels in archival specimens by immunohistochemical analysis. RESULTS: Cyr61 and TF are expressed at elevated levels in cell lines of uveal melanoma compared with normal uveal melanocytes. Duplication of a region of chromosome arm 1p, encompassing the genes encoding Cyr61 and TF, was observed in the melanoma cell line used in the initial subtractive hybridization. Both genes are also expressed in primary uveal melanomas, and a correlation was found between expression of TF and the number of blood vessels in archival specimens. CONCLUSIONS: Cyr61 and TF may contribute to the angiogenic phenotype associated with uveal melanoma. A region of chromosome arm 1p also may contain oncogenes or tumor suppressor genes pertinent to the origins of this type of ocular tumor. CLINICAL RELEVANCE: New immunotherapies have been devised for the treatment of cancer based on the expression of TF. Similar approaches may be effective in treating uveal melanoma.


Subject(s)
Immediate-Early Proteins/genetics , Intercellular Signaling Peptides and Proteins/genetics , Melanoma/metabolism , Thromboplastin/genetics , Uveal Neoplasms/metabolism , Blotting, Western , Chromosomes, Human, Pair 1/genetics , Cysteine-Rich Protein 61 , Cytogenetics , Endothelial Growth Factors/metabolism , Humans , Immediate-Early Proteins/metabolism , Immunoenzyme Techniques , In Situ Hybridization, Fluorescence , Intercellular Signaling Peptides and Proteins/metabolism , Lymphokines/metabolism , Melanoma/blood supply , Neovascularization, Pathologic/pathology , RNA, Messenger/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Thromboplastin/metabolism , Tumor Cells, Cultured , Uveal Neoplasms/blood supply , Vascular Endothelial Growth Factor A , Vascular Endothelial Growth Factors
13.
J Agric Food Chem ; 50(22): 6346-52, 2002 Oct 23.
Article in English | MEDLINE | ID: mdl-12381115

ABSTRACT

Membrane and resin ion-exchange technology was used for pH reduction and production of Cynthiana (Vitis aestivalis) wine, which can have high pH and high titratable acidity. Wine attributes were monitored during storage for 6 months at 21 and 38 degrees C. Nonadjusted Cynthiana wine (pH 4.1) was compared to ion-exchange-adjusted wine (pH 3.5). Ion exchange lowered the pH and potassium content and increased the titratable acidity of wine without having detrimental effects on color and phenolics. No trends were found to indicate differences between manufacturers of membranes and resins on pH-adjusted Cynthiana wine. Wine treated with membrane ion exchange was higher in color density and phenolics than resin-treated wine. During storage at both temperatures, the quality of the wine decreased, with greater degradation at 38 degrees C. Ion exchange decreased the pH of Cynthiana wine without negatively affecting wine quality attributes. A panel familiar with characteristics of Cynthiana wine found that the color and flavor of the pH-adjusted wine was improved.


Subject(s)
Food Handling/methods , Vitis/chemistry , Wine/analysis , Wine/standards , Color , Hydrogen-Ion Concentration , Hydroxybenzoates/analysis , Ion Exchange Resins , Membranes, Artificial , Taste , Temperature , Time Factors
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