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1.
Eur J Nutr ; 59(4): 1463-1472, 2020 Jun.
Article in English | MEDLINE | ID: mdl-31119400

ABSTRACT

PURPOSE: Aim of this study was to identify a possible relationship among dietary fatty acids (FA) intake, FA adipose tissue (AT) profile and cancer condition in lean vs obese subjects affected or not by colorectal cancer (CRC). Actually, inadequate dietary habits together with physical inactivity are primary determinants of obesity and cancer risk. Changes in lipid metabolism play a crucial role in different types of cancer and key enzymes involved in lipid-metabolic pathways, such as stearoyl-coA-desaturase 1 (SCD-1), are differentially expressed in normal and cancer tissues. METHODS: Food frequency questionnaires (FFQ) were analyzed by Winfood software. FA were assessed by gas-liquid chromatography in visceral AT samples. Estimated desaturase activities were calculated as precursor FA/product FA ratio. Desaturase gene expressions were evaluated by RT-qPCR. RESULTS: Lean and obese CRC subjects showed inadequate dietary habits. In particular, lean CRC subjects showed increase in the intake of saturated FA, specifically palmitic (p = 0.0042) and stearic acid (p = 0.0091), and a corresponding reduction of monounsaturated FA consumption, in particular oleic acid (p = 0.002) with respect to lean without CRC. Estimated SCD-1 activity in AT was increased in all the groups vs lean without CRC (pANOVA = 0.029). CONCLUSIONS: Unhealthy eating habits, characterizing obese and CRC subjects, may influence the visceral AT profile and contribute to the alteration of the metabolic pathways. The quality of the diet, other than the quantity, can have a main role in the establishment of inflammatory microenvironment and in metabolic changes favouring CRC.


Subject(s)
Colorectal Neoplasms/blood , Diet/adverse effects , Diet/methods , Fatty Acids/blood , Intra-Abdominal Fat/metabolism , Obesity/blood , Adult , Aged , Female , Humans , Male , Middle Aged
2.
J Endocrinol Invest ; 39(11): 1295-1301, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27344308

ABSTRACT

AIM: Phenolic compounds naturally contained in extra-virgin olive oil (EVOO) have demonstrated anti-inflammatory and antioxidant properties. The present study aimed at evaluating the effects of a polyphenol-rich extra-virgin olive oil (EVOO) (high-polyphenol EVOO, HP-EVOO) on the metabolic control and the production of specific pro-/anti-inflammatory adipokines in overweight patients with type 2 diabetes mellitus (T2D). METHODS: Eleven overweight T2D patients not in treatment with insulin were invited to follow their habitual diet for a total of 8 weeks. During the first 4 weeks (wash-out period), they were asked to consume refined olive oil (ROO, polyphenols not detectable) and then to replace ROO with HP-EVOO (25 mL/day, 577 mg of phenolic compounds/kg) for the remaining 4 weeks. Anthropometric parameters, fasting glycaemia, glycated haemoglobin (HbA1c), high-sensitive C-reactive protein, plasma lipid profile, liver function and serum levels of TNF-α, IL-6, adiponectin, visfatin and apelin were assessed at the end of each 4-week period. RESULTS: HP-EVOO consumption significantly reduced fasting plasma glucose (P = 0.023) and HbA1c (P = 0.039) levels as well as BMI (P = 0.012) and body weight (P = 0.012). HP-EVOO ingestion determined a reduction in serum level of aspartate aminotransferase (AST, P = 0.0056) and alanine aminotransferase (ALT, P = 0.024). Serum visfatin levels strongly decreased after HP-EVOO ingestion (P = 0.0021). CONCLUSIONS: Daily consumption of polyphenol-rich EVOO might improve metabolic control and circulating inflammatory adipokines profile in overweight T2D patients.


Subject(s)
Biomarkers/blood , Diabetes Mellitus, Type 2/metabolism , Nicotinamide Phosphoribosyltransferase/blood , Olive Oil/chemistry , Phenols/administration & dosage , Administration, Oral , Cytokines/blood , Diabetes Mellitus, Type 2/drug therapy , Diabetes Mellitus, Type 2/etiology , Female , Humans , Male , Middle Aged , Overweight/complications
3.
Curr Med Chem ; 19(18): 2901-17, 2012.
Article in English | MEDLINE | ID: mdl-22519395

ABSTRACT

Epidemiological evidence has shown that a high dietary intake of vegetables and fruit rich in polyphenols is associated with a reduction of cancer incidence and mortality from coronary heart disease. The healthy effects associated with polyphenol consumption have made the study of the mechanisms of action a matter of great importance. In particular, the hydroxybenzoic acid protocatechuic acid (PCA) has been eliciting a growing interest for several reasons. Firstly, PCA is one of the main metabolites of complex polyphenols such as anthocyanins and procyanidins that are normally found at high concentrations in vegetables and fruit, and are absorbed by animals and humans. Since the daily intake of anthocyanins has been estimated to be much higher than that of other polyphenols, the nutritional value of PCA is increasingly recognized. Secondly, a growing body of evidence supports the concept that PCA can exert a variety of biological effects by acting on different molecular targets. It has been shown that PCA possesses antioxidant, anti-inflammatory as well as antihyperglycemic and neuroprotective activities. Furthermore, PCA seems to have chemopreventive potential because it inhibits the in vitro chemical carcinogenesis and exerts pro-apoptotic and anti-proliferative effects in different tissues. This review is aimed at providing an up-dated and comprehensive report on PCA giving a special emphasis on its biological activities and the molecular mechanisms of action most likely responsible for a beneficial role in human disease prevention.


Subject(s)
Anti-Infective Agents/pharmacology , Anti-Inflammatory Agents/pharmacology , Antioxidants/pharmacology , Hydroxybenzoates/pharmacology , Animals , Anti-Infective Agents/pharmacokinetics , Anti-Inflammatory Agents/pharmacokinetics , Antioxidants/pharmacokinetics , Apoptosis/drug effects , Diet , Humans , Hydroxybenzoates/pharmacokinetics
4.
J Endocrinol Invest ; 34(5): e110-4, 2011 May.
Article in English | MEDLINE | ID: mdl-20926921

ABSTRACT

BACKGROUND: Fasting and post-prandial abnormalities of adipose tissue (AT) lipoprotein lipase (LPL) and hormone- sensitive lipase (HSL) activities may have pathophysiological relevance in insulin-resistant conditions. AIM: The aim of this study was to evaluate activity and gene expression of AT LPL and HSL at fasting and 6 h after meal in two insulin-resistant groups - obese with Type 2 diabetes and obese without diabetes - and in non-diabetic normal-weight controls. MATERIAL/SUBJECTS AND METHODS: Nine obese subjects with diabetes, 10 with obesity alone, and 9 controls underwent measurements of plasma levels of glucose, insulin, and triglycerides before and after a standard fat-rich meal. Fasting and post-prandial (6 h) LPL and HSL activities and gene expressions were determined in abdominal subcutaneous AT needle biopsies. RESULTS: The diabetic obese subjects had significantly lower fasting and post-prandial AT heparin-releasable LPL activity than only obese and control subjects (p<0.05) as well as lower mRNA LPL levels. HSL activity was significantly reduced in the 2 groups of obese subjects compared to controls in both fasting condition and 6 h after the meal (p<0.05), while HSL mRNA levels were not different. There were no significant changes between fasting and 6 h after meal measurements in either LPL or HSL activities and gene expressions. CONCLUSIONS: Lipolytic activities in AT are differently altered in obesity and Type 2 diabetes being HSL alteration associated with both insulin-resistant conditions and LPL with diabetes per se. These abnormalities are similarly observed in the fasting condition and after a fat-rich meal.


Subject(s)
Adipose Tissue/enzymology , Diabetes Mellitus, Type 2/enzymology , Fasting , Lipoprotein Lipase/metabolism , Obesity/enzymology , Postprandial Period , Sterol Esterase/metabolism , Adipose Tissue/physiology , Blood Glucose/metabolism , Body Mass Index , Diabetes Mellitus, Type 2/physiopathology , Humans , Insulin/blood , Insulin Resistance/physiology , Lipoprotein Lipase/genetics , Obesity/physiopathology , RNA, Messenger/metabolism , Sterol Esterase/genetics , Triglycerides/blood
6.
J Am Dent Assoc ; 132(3): 361-7, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11258093

ABSTRACT

BACKGROUND: Serving as a forensic consultant or medical expert witness is a professional duty and social responsibility. While objectivity is a hallmark of ethical health care evaluation, conflict arises when medical experts exhibit bias and serve the hiring party's interests instead of the public's. METHODS: The authors define different types of expert witnesses and examine the means for improving the quality of testimony. They evaluate professional association codes of ethics, health care education, neutral medical experts and the field of bioethics. RESULTS: Incorporating case-based analysis of medical expert testimony in the education of health care professionals may elevate the caliber of testimony. Court-appointed neutral experts may overcome some of the problems inherent in professional and product liability litigation. Neutral bioethicists may play a constructive role in mediating medicolegal disputes. Adopting strong professional association codes of ethics requires the consent of all members, and loss of membership for ethics violations may not be a powerful enough deterrent to biased testimony. CONCLUSION: Biased testimony contributes to scientifically unfounded liability verdicts. The public ultimately pays for huge monetary settlements via higher costs for all goods and services. Financial incentives in the current professional and product liability system will make it difficult to institute court-appointed neutral expert panels on a widespread basis. PRACTICE IMPLICATIONS: Dentists should view themselves as clinicians and evaluators. Rendering expert opinions on forensic matters is an ethical part of dental practice. By doing so with honesty and objectivity, dentists serve as a bridge to justice and fulfill a social responsibility.


Subject(s)
Ethics, Dental , Expert Testimony , Bioethics , Conflict of Interest , Education, Dental , Expert Testimony/standards , Forensic Dentistry/classification , Forensic Dentistry/education , Forensic Dentistry/standards , Humans , Liability, Legal/economics , Prejudice , Professional Competence/legislation & jurisprudence , Professional Competence/standards , Public Opinion , Social Justice , Social Responsibility
7.
Clin Sci (Lond) ; 100(2): 191-8, 2001 Feb.
Article in English | MEDLINE | ID: mdl-11171288

ABSTRACT

Several studies have suggested that the oxidative modification of low-density lipoprotein (LDL) could play a key role in the early stages of atherosclerosis. The susceptibility of LDL to oxidation has been found to be greater in patients with coronary heart disease. Familial hypercholesterolaemia (FH) is a powerful clinical model in which to study the predictive role of LDL in atherogenesis. LDL-apheresis is a treatment that is able to decrease lipid levels in plasma. This study was aimed at investigating the reducing capacity of erythrocytes and the in vitro susceptibility to oxidation of LDL isolated from patients with homozygous, heterozygous and double-heterozygous FH, who were treated fortnightly with LDL-apheresis or left untreated. In 14 FH patients, at baseline and after a cycle of treatment, the susceptibility of LDL to oxidative modification was analysed by studying the kinetics of conjugate diene formation. Plasma hydroperoxides, polyunsaturated fatty acid content, LDL electrophoretic mobility on agarose, the titre of auto-antibodies against oxidized LDL and serum paraoxonase activity were also measured. Furthermore, in order to evaluate a potential relationship between LDL oxidation and redox status, erythrocyte GSH and ATP levels were determined in FH patients treated regularly or never treated previously by LDL-apheresis. Unlike in the control group, the oxidative status of LDL in all FH patients was modified by LDL-apheresis, as revealed by the higher negative charge and the increase in levels of hydroperoxides and antibodies against oxidized LDL in the plasma. Our findings suggest both an acute effect and a long-term effect of LDL-apheresis in FH patients treated with dextran sulphate cellulose apheresis. The acute effect of LDL-apheresis on the susceptibility to oxidation of plasma and LDL was demonstrated by significant decreases in plasma hydroperoxide content, total LDL concentration and polyunsaturated fatty acid content. The increased resistance of LDL to oxidation was shown by prolongation of the lag time (P<0.05) in samples after a single cycle of treatment. The long-term effect of LDL-apheresis was demonstrated by the comparable values for lag phases (obtained from the kinetics of conjugate diene formation) in patients under active treatment and controls. Compared with healthy controls and untreated patients, the erythrocyte GSH content was significantly higher (P

Subject(s)
Erythrocytes/physiology , Hyperlipoproteinemia Type II/therapy , Lipoproteins, LDL/blood , Plasmapheresis , Adenosine Triphosphate/blood , Adolescent , Adult , Child , Child, Preschool , Electrophoresis, Agar Gel , Erythrocytes/metabolism , Fatty Acids, Unsaturated/blood , Female , Glutathione/blood , Humans , Hyperlipoproteinemia Type II/blood , Lipid Peroxides/blood , Lipoproteins, LDL/physiology , Male , Middle Aged , Oxidation-Reduction
8.
Immunology ; 104(4): 431-8, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11899429

ABSTRACT

This study investigates the in vitro effects of oxidized low-density lipoproteins (ox-LDL), 'physiological' pro-oxidants, N-acetylcysteine (NAC), a free radical scavenger and glutathione precursor, and their combination on human peripheral blood mononuclear cell functions. We found that treatment with ox-LDL induced a significant down-regulation of proliferative response to mitogens, antigens and interleukin-2. Lipid extracts from ox-LDL were able to reproduce the same effect as the lipoprotein. On the other hand, NAC exposure induced a significant up-regulation of proliferative responses to all the stimuli used. Moreover, we showed that natural killer (NK) cell-mediated cytotoxic activity was significantly down-regulated by ox-LDL while treatment with NAC induced a significant up-regulation of NK-cell activity. Finally, we found that ox-LDL and NAC exerted opposite effects on the cytokine network, interfering both at the protein secretion level and the messenger RNA synthesis level. More importantly, when NAC was used in combination with ox-LDL the proliferative responses, NK-cell-mediated cytotoxic activity and cytokine production were restored to values comparable to controls. These data indicate that ox-LDL and NAC modulate immune functions, exerting opposite effects reflecting their pro-oxidant and antioxidant behaviours. Our results add new insights to the key role played by redox imbalance as a modulator of immune system homeostasis and suggest that an antioxidant drug such as NAC could be useful against pathologies associated with an increase in lipid peroxidation.


Subject(s)
Acetylcysteine/pharmacology , Free Radical Scavengers/pharmacology , Leukocytes, Mononuclear/drug effects , Lipoproteins, LDL/pharmacology , Oxidative Stress/immunology , Cell Division/drug effects , Cells, Cultured , Cytokines/biosynthesis , Cytotoxicity, Immunologic/drug effects , Down-Regulation/drug effects , Humans , Killer Cells, Natural/drug effects , Killer Cells, Natural/immunology , Leukocytes, Mononuclear/immunology , Lymphocyte Activation/drug effects , Mitogens/immunology , Oxidation-Reduction , Up-Regulation/drug effects
9.
Todays FDA ; 13(2): 24-5, 2001 Feb.
Article in English | MEDLINE | ID: mdl-15025038

ABSTRACT

The remodeling of the PDL and alveolar bone that occurs during orthodontic tooth movement (OTM) has long been associated with an inflammatory process. The vascular and cellular changes that occur have been well documented, and several inflammatory mediators, growth factors and neuropeptides have been found in increased levels in the periodontal supporting tissues during orthodontic tooth movement. It recently was found that peripheral nerve fibers participate in the inflammatory process (neurogenic inflammation) by releasing various neuropeptides. Calcitonin gene-related peptide (CGRP) and substance P (SP), two PDL neuropeptides, play a role in inflammation by serving as vasodilators and inducing increased vascular permeability. They also stimulate plasma extravasation and proliferation of endothelial cells and fibroblasts; upregulate the expression of endothelial cell adhesion molecules; and act as neurotransmitters. The increase in concentration of these PDL neuropeptides during OTM indicates their importance to the process. This paper will review the current research and summarize the roles and proposed mechanism of these two main PDL neurotransmitters in OTM.


Subject(s)
Calcitonin Gene-Related Peptide/physiology , Periodontal Ligament/physiology , Substance P/physiology , Tooth Movement Techniques , Humans , Inflammation/physiopathology , Periodontal Ligament/innervation
10.
Lipids ; 36(11): 1195-202, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11795851

ABSTRACT

The aim of this study was to assess the effects of the dietary intake of extra virgin olive oil on the oxidative susceptibility of low density lipoproteins (LDL) isolated from the plasma of hyperlipidemic patients. Ten patients with combined hyperlipidemia (mean plasma cholesterol 281 mg/dL, triglycerides 283 mg/dL) consumed a low-fat, low-cholesterol diet, with olive oil (20 g/d) as the only added fat, with no drug or vitamin supplementation for 6 wk. Then they were asked to replace the olive oil they usually consumed with extra virgin olive oil for 4 wk. LDL were isolated at the beginning, and after the 4 wk of dietary treatment. LDL susceptibility to CuSO4-mediated oxidation was evaluated by measuring the extent of lipid peroxidation. We also determined fatty acid composition and vitamin E in plasma and LDL and plasma phenolic content. Extra virgin olive oil intake did not affect fatty acid composition of LDL but significantly reduced the copper-induced formation of LDL hydroperoxides and lipoperoxidation end products as well as the depletion of LDL linoleic and arachidonic acid. A significant increase in the lag phase of conjugated diene formation was observed after dietary treatment. These differences are statistically correlated with the increase in plasma phenolic content observed at the end of the treatment with extra virgin olive oil; they are not correlated with LDL fatty acid composition or vitamin E content, which both remained unmodified after the added fat change. This report suggests that the daily intake of extra virgin olive oil in hyperlipidemic patients could reduce the susceptibility of LDL to oxidation, not only because of its high monounsaturated fatty acid content but probably also because of the antioxidative activity of its phenolic compounds.


Subject(s)
Hyperlipidemias/blood , Lipoproteins, LDL/metabolism , Plant Oils/pharmacology , Adult , Aged , Diet , Fatty Acids/analysis , Female , Humans , Hyperlipidemias/drug therapy , Lipoproteins, LDL/chemistry , Lipoproteins, LDL/drug effects , Male , Middle Aged , Olive Oil , Oxidation-Reduction , Vitamin E/blood
13.
Biochem Biophys Res Commun ; 273(3): 899-901, 2000 Jul 14.
Article in English | MEDLINE | ID: mdl-10891344

ABSTRACT

Fanconi's anemia (FA) is a clinically and genetically heterogeneous disease which has been hypothesized to be defective in the detoxification of reactive oxygen species. In this work we report the results obtained by morphometric analyses on the red blood cells (RBCs) from FA patients and their parents. We found that a high rate of erythrocytes from both homozygous and heterozygous subjects was significantly altered. RBCs underwent in fact cytoskeleton-dependent modifications, in particular of spectrin molecule, leading to cell shrinking and blebbing. We hypothesize that these changes may be the result of an oxidative imbalance that probably lead to alterations of RBC plasticity- and deformation-associated functions. Moreover, our results also suggest the possibility to identify FA carriers by the existence of RBC abnormalities.


Subject(s)
Erythrocytes/metabolism , Fanconi Anemia/blood , Spectrin/metabolism , Adolescent , Adult , Child , Child, Preschool , Fanconi Anemia/genetics , Heterozygote , Humans , Phenotype
14.
Lipids ; 35(1): 45-54, 2000 Jan.
Article in English | MEDLINE | ID: mdl-10695923

ABSTRACT

On the basis of the results obtained with pilot studies conducted in vitro on human low density lipoprotein (LDL) and on cell cultures (Caco-2), which had indicated the ability of certain molecules present in olive oil to inhibit prooxidative processes, an in vivo study was made of laboratory rabbits fed special diets. Three different diets were prepared: a standard diet for rabbits (diet A), a standard diet for rabbits modified by the addition of 10% (w/w) extra virgin olive oil (diet B), a modified standard diet for rabbits (diet C) differing from diet B only in the addition of 7 mg kg(-1) of oleuropein. A series of biochemical parameters was therefore identified, both in the rabbit plasma and the related isolated LDL, before and after Cu-induced oxidation. The following, in particular, were selected: (i) biophenols, vitamins E and C, uric acid, and total, free, and ester cholesterol in the plasma; (ii) proteins, triglycerides, phospholipids, and total, free, and ester cholesterol in the native LDL (for the latter, the dimensions were also measured); (iii) lipid hydroperoxides, aldehydes, conjugated dienes, and relative electrophoretic mobility (REM) in the oxidized LDL (ox-LDL). In an attempt to summarize the results obtained, it can be said that this investigation has not only verified the antioxidant efficacy of extra virgin olive oil biophenols and, in particular, of oleuropein, but has also revealed a series of thus far unknown effects of the latter on the plasmatic lipid situation. In fact, the addition of oleuropein in diet C increased the ability of LDL to resist oxidation (less conjugated diene formation) and, at the same time, reduced the plasmatic levels of total, free, and ester cholesterol (-15, -12, and -17%, respectively), giving rise to a redistribution of the lipidic components of LDL (greater phospholipid and cholesterol amounts) with an indirect effect on their dimensions (bigger by about 12%).


Subject(s)
Lipoproteins, LDL/blood , Pyrans/pharmacology , Animals , Ascorbic Acid/blood , Cholesterol/blood , Chromatography, High Pressure Liquid , Copper/pharmacology , Dietary Fats/administration & dosage , Female , Iridoid Glucosides , Iridoids , Lipid Peroxidation/drug effects , Olive Oil , Plant Oils/administration & dosage , Rabbits , Triglycerides/blood , Uric Acid/blood , Vitamin E/blood
15.
FEBS Lett ; 468(2-3): 125-8, 2000 Feb 25.
Article in English | MEDLINE | ID: mdl-10692571

ABSTRACT

Fanconi's anemia (FA) is a very rare genetically heterogeneous disease which has been hypothesized to be defective in the detoxification of reactive oxygen species. In this work we report the results obtained by morphometric and biochemical analyses on the red blood cells (RBCs) from FA patients. With respect to RBCs from healthy donors the following changes have been detected: (i) a variety of ultrastructural alterations, mainly surface blebbing typical of acanthocytes and stomatocytes; (ii) a significant quantitative increase of these altered forms; (iii) modifications of spectrin cytoskeleton network; (iv) an altered redox balance, e.g. a decreased catalase activity and significant variations in the GSSG/GSH ratio. We hypothesize that remodeling of the redox state occurring in FA patients results in cytoskeleton-associated alterations of red blood cell integrity and function.


Subject(s)
Cytoskeleton/ultrastructure , Erythrocyte Membrane/ultrastructure , Erythrocytes/metabolism , Erythrocytes/ultrastructure , Fanconi Anemia/blood , Adolescent , Adult , Catalase/blood , Child , Child, Preschool , Glutathione/blood , Glutathione Disulfide/blood , Humans , Microscopy, Electron, Scanning , Reference Values , Spectrin/ultrastructure , Superoxide Dismutase/blood , Superoxides/blood , Zinc/blood
16.
Photochem Photobiol ; 71(1): 97-102, 2000 Jan.
Article in English | MEDLINE | ID: mdl-10649896

ABSTRACT

Oxidized LDL (ox-LDL) have been involved in the pathogenesis of several human diseases including dermatological pathologies. Oxidative modification of low-density lipoproteins (LDL) is accompanied by both extensive degradation of its polyunsaturated fatty acids and production of lipoperoxides. These highly reactive products induce an intracellular oxidative stress with a variety of cytotoxic effects. In order to evaluate cellular damage induced by oxidative stress in epidermal cells, a human epidermoid carcinoma cell line in culture (A 431) was used as experimental model. Cell treatment with UV-oxidized LDL resulted in cytostatic and cytotoxic effects characterized by morphological and functional alterations: inhibition of cell proliferation, modifications of cytoskeleton network, microtubular derangement, loss of cell-cell and cell-substrate contacts, cell detachment and cell death by apoptosis. The ox-LDL-induced alterations were almost completely prevented by pre-incubating cells with alpha-tocopherol. The results presented here could be of relevance for a better comprehension of the pathogenic mechanisms of several human diseases, including dermatological pathologies, and could indicate that antioxidants such as alpha-tocopherol could represent an important therapeutic challenge in the maintenance of cell and tissue homeostasis in the long run.


Subject(s)
Lipoproteins, LDL/physiology , Vitamin E/pharmacology , Epithelial Cells/drug effects , Epithelial Cells/metabolism , Epithelial Cells/ultrastructure , Humans , Lipoproteins, LDL/radiation effects , Microscopy, Electron, Scanning , Oxidative Stress , Subcellular Fractions/drug effects , Subcellular Fractions/metabolism , Tumor Cells, Cultured , Ultraviolet Rays
17.
Mol Genet Metab ; 71(4): 651-5, 2000 Dec.
Article in English | MEDLINE | ID: mdl-11136559

ABSTRACT

This paper shows for the first time the higher oxidizability of low-density lipoprotein (LDL) in plasma from adrenoleukodystrophy (ALD) patients compared to that of control subjects. LDL oxidation susceptibility was assessed by conjugate diene formation, hydroperoxide and lipoperoxide formation, and electrophoretic mobility. Simvastatin therapy, an HMG-CoA reductase inhibitor, seems to be a protective pharmacological agent against the higher oxidizability of LDL in plasma from ALD patients.


Subject(s)
Adrenoleukodystrophy/drug therapy , Adrenoleukodystrophy/metabolism , Lipid Peroxidation/drug effects , Lipoproteins, LDL/metabolism , Simvastatin/pharmacology , Simvastatin/therapeutic use , Adrenoleukodystrophy/blood , Humans , Hydrogen Peroxide/metabolism , Hydroxymethylglutaryl-CoA Reductase Inhibitors/pharmacology , Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use , Hypolipidemic Agents/pharmacology , Hypolipidemic Agents/therapeutic use , Kinetics , Lipid Peroxides/metabolism , Lipoproteins, LDL/blood , Male , Oxidation-Reduction/drug effects , Oxidative Stress/drug effects , Phenotype
18.
Redox Rep ; 4(3): 113-21, 1999.
Article in English | MEDLINE | ID: mdl-10496414

ABSTRACT

Olive oil contains several phenolic compounds with antioxidant activity, whose levels depend strongly on the kind of cultivar grown, fruit ripening effects and the oil extraction process. Therefore, the beneficial effects exerted by olive oil consumption on the resistance of low density lipoproteins (LDLs) to oxidation depend not only on an increased intake of mono-unsaturated fatty acids (e.g. oleate) which are less prone to oxidation, but also phenolic antioxidants. The aim of this study was to analyze in vitro effects exerted on the oxidative modification of Cu-stimulated human LDL by two olive oil biophenols, i.e. 3,4-dihydroxyphenylethanol-elenolic acid (3,4-DHPEA-EA) and protocatecuic acid. These compounds have not been investigated in as much detail as the better-known olive oil biophenols - such as tyrosol (p-HPEA), o-coumaric acid, vanillic acid, caffeic acid, oleuropein and 3,4-dihydroxyphenylethanol (3,4-DHPEA). Modification of LDL was tested by measuring the formation of intermediate and end products of lipid peroxidation such as conjugated dienes, lipid hydroperoxides, cholesterol and cholesteryl ester oxides, as well as studying the decrease in oxidizable substrates like polyunsaturated fatty acids. In addition, the increase in LDL negative charges was evaluated. The results demonstrate the two-tested olive oil biophenols show high antioxidant activities. In particular, protocatecuic acid and 3,4-DHPEA-EA show an antioxidant activity comparable with that of caffeic acid, oleuropein and 3,4-DHPEA. They are not only able to retard lipid peroxidation, but also to reduce the extent of its activity.


Subject(s)
Antioxidants/pharmacology , Hydroxybenzoates/pharmacology , Lipid Peroxides/analysis , Lipoproteins, LDL/blood , Phenols/pharmacology , Plant Oils/chemistry , Pyrans/pharmacology , Antioxidants/isolation & purification , Arachidonic Acid/analysis , Cholesterol/analysis , Fatty Acids/analysis , Humans , Hydroxybenzoates/isolation & purification , Linoleic Acid/analysis , Lipoproteins, LDL/drug effects , Lipoproteins, LDL/isolation & purification , Olive Oil , Phenols/isolation & purification , Plant Oils/pharmacology , Pyrans/isolation & purification
19.
J Nutr ; 129(7): 1269-77, 1999 Jul.
Article in English | MEDLINE | ID: mdl-10395586

ABSTRACT

Experimental and clinical evidence suggest that oxidative stress causes cellular damage, leading to functional alterations of the tissue. Free radicals may thus play an important role in the pathogenesis of a number of human diseases. Among pro-oxidant agents, oxidized LDL lead to the production of cytotoxic reactive species, e.g., lipoperoxides, causing tissue injury and various subsequent pathologies including intestinal diseases. Thus, to analyze the oxidative damage induced by oxidized LDL to intestinal mucosa, we evaluated morphological and functional changes induced in the human colon adenocarcinoma cell line, Caco-2. In addition, we examined the protective effects exerted by tyrosol, 2-(4-hydroxyphenyl)ethanol, the major phenolic compound present in olive oil. Caco-2 cell treatment (24 and/or 48 h) with oxidized LDL (0.2 g/L) resulted in cytostatic and cytotoxic effects characterized by a series of morphological and functional alterations: membrane damage, modifications of cytoskeleton network, microtubular disorganization, loss of cell-cell and cell-substrate contacts, cell detachment and cell death. The oxidized LDL-induced alterations in Caco-2 cells were almost completely prevented by tyrosol which was added 2 h before and present during the treatments. Our results suggest that some biophenols, such as those contained in olive oil, may counteract the reactive oxygen metabolite-mediated cellular damage and related diseases, by improving in vivo antioxidant defenses.


Subject(s)
Antioxidants/pharmacology , Caco-2 Cells/drug effects , Intestinal Mucosa/drug effects , Lipoproteins, LDL/drug effects , Oxidative Stress/drug effects , Phenylethyl Alcohol/analogs & derivatives , Analysis of Variance , Antioxidants/therapeutic use , Caco-2 Cells/metabolism , Caco-2 Cells/ultrastructure , Humans , Intestinal Mucosa/metabolism , L-Lactate Dehydrogenase/metabolism , Oxidation-Reduction/drug effects , Phenylethyl Alcohol/pharmacology , Phenylethyl Alcohol/therapeutic use , Reactive Oxygen Species/metabolism
20.
Exp Gerontol ; 34(1): 47-57, 1999 Jan.
Article in English | MEDLINE | ID: mdl-10197727

ABSTRACT

Successful aging, characterized by little or no loss in physiological functions, should be the usual aging process in centenarians. It is known that well-preserved physiological functions depend on the proper functioning of cell systems. In this article we focus on cell membrane integrity and study the red blood cell membrane to evaluate the effect of physiological aging in centenarians. Fifteen healthy, self-sufficient centenarians, mean age 103 years, were examined by assessing hemocytometric values and some relevant characteristics of the erythrocyte membrane, i.e., the cholesterol/phospholipid molar ratio, the distribution of phospholipid classes and their fatty acid composition, the integral and skeletal protein profiles. The centenarians showed a significant decrease in the red blood cell count (p < 0.0002), hemoglobin (p < 0.0002), and hematocrit (p < 0.0005). The red blood cell membrane showed a significantly increased cholesterol/phospholipid molar ratio (p < 0.01), with a concomitant increase in polyunsaturated fatty acids in phosphatidylcholine (p < 0.001) and, to a lesser extent, in phosphatidylethanolamine. The electrophoretic pattern of membrane proteins was qualitatively normal compared to controls but the densitometric analysis showed a significant increase in the integral protein band 4.2 (p < 0.05) and in the skeletal protein actin (p < 0.001). Extreme longevity seems to be associated with a substantial integrity of the erythrocyte membrane. Moreover, the evident increase in polyunsaturated fatty acids and in actin are likely to improve the membrane fluidity and to strengthen the membrane structure.


Subject(s)
Aging/blood , Erythrocyte Membrane/chemistry , Aged , Aged, 80 and over , Female , Humans , Longevity , Male , Membrane Lipids/blood , Membrane Proteins/blood
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