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1.
Menopause ; 17(4): 766-71, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20386345

ABSTRACT

OBJECTIVE: The aim of this study was to evaluate the effect of 17beta-estradiol, raloxifene, and 1-alpha,25-dihydroxycholecalciferol or calcitriol on bone and lipid metabolism in chronic kidney disease and estrogen insufficiency. METHODS: Six-month-old female Sprague-Dawley rats (n = 48) were ovariectomized and nephrectomized (seven eighths). One week after surgery, the rats were divided into six groups and treated with (1) placebo, (2) 17beta-estradiol 10 microg kg day, (3) raloxifene 1 mg kg day, (4) calcitriol 10 ng kg day, (5) 17beta-estradiol + calcitriol, and (6) raloxifene + calcitriol. A group of untreated animals with chronic kidney disease and normal ovarian function was used as a control group (n = 5). The rats were killed after 8 weeks of treatment. Blood samples were drawn for serum analyses; the right tibia was removed to perform histomorphometric analyses, uteri were used as tissue markers of estrogen replacement, and paraffin-embedded sections of the uterus and the fourth breast were used for histopathologic evaluation. RESULTS: Raloxifene, alone or combined with calcitriol, and 17beta-estradiol combined with calcitriol significantly diminished total cholesterol level compared with placebo. Qualitative histological and histomorphometric analyses showed that both the single treatments and their combinations were able to increase the trabecular connectivity compared with placebo. The less beneficial results were obtained with 17beta-estradiol alone, whereas the more beneficial results were obtained with the combined treatments, particularly with raloxifene and calcitriol. CONCLUSIONS: In summary, this experimental study demonstrates the advantages of replacing both hormonal deficiencies together. The combination of calcitriol and raloxifene, a selective estrogen receptor modulator, showed a better lipid, uterus, and bone profile.


Subject(s)
Cholesterol/blood , Estradiol/pharmacology , Estrogens/deficiency , Kidney Diseases/complications , Raloxifene Hydrochloride/pharmacology , Tibia/metabolism , Animals , Atrophy , Bone Density Conservation Agents/pharmacology , Calcitriol/pharmacology , Calcium/blood , Chronic Disease , Estrogens/pharmacology , Female , Hyperplasia , Mammary Glands, Animal/pathology , Organ Size , Parathyroid Hormone/blood , Phosphorus/blood , Rats , Rats, Sprague-Dawley , Selective Estrogen Receptor Modulators/pharmacology , Tibia/pathology , Uterus/pathology
2.
Can J Appl Physiol ; 30(1): 18-32, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15855680

ABSTRACT

The aim of this study was to assess the food habits and nutritional status of high level adolescent soccer players (N = 33; ages 14-16 yrs) living in their home environment. Body composition (height, mass, skinfolds), biochemical and hematological parameters, performance in soccer-specific tests (sprinting, jumping, intermittent endurance), and dietary intake (weighed food intake method) and related behaviors (nutrient supplement use, daily activity profile) were assessed. Daily energy expenditure and energy intake were 12.5 MJ and 12.6 MJ, respectively. Protein (16% of energy intake; 1.9 g/kg of body mass), lipid (38%), and cholesterol (385 mg) intake were above recommendations, while carbohydrates (45%) were below. The food intake of these adolescents was based on cereals and derivates; meat, fish, and eggs; milk and dairy products; biscuits and confectionery; and oil, butter and margarine, which provided 78% of total energy intake, 85% of proteins, 64% of carbohydrates, 90% of lipids, and 47% of fiber. Although diet provided sufficient iron, 48% of individuals showed iron deficiency without anemia. Based on these results, a well designed nutrition intervention would be advisable for optimizing performance, and especially for promoting healthy eating habits in adolescent soccer players.


Subject(s)
Feeding Behavior , Nutrition Assessment , Nutritional Status , Soccer , Adolescent , Body Composition , Body Height , Body Mass Index , Cholesterol, Dietary/administration & dosage , Dietary Carbohydrates/administration & dosage , Dietary Fats/administration & dosage , Dietary Fiber/administration & dosage , Dietary Proteins/administration & dosage , Dietary Supplements , Energy Intake , Energy Metabolism/physiology , Humans , Male , Motor Activity/physiology , Physical Endurance/physiology , Psychomotor Performance/physiology , Running/physiology , Skinfold Thickness , Soccer/physiology
3.
Pediatr Nephrol ; 18(2): 110-4, 2003 Feb.
Article in English | MEDLINE | ID: mdl-12579398

ABSTRACT

The purpose of the study was to determine whether DNA polymorphisms at the renin-angiotensin-aldosterone (RAS) genes were associated with evolution to renal scar formation and, consequently, with reflux nephropathy (RN) in patients with vesicoureteral reflux (VUR). Some authors have suggested that the DD genotype of the angiotensin-converting enzyme (ACE) gene would be an adverse renal prognosis factor. We recruited 246 patients (aged 3 months to 22 years) from four Spanish hospitals. These included 69 patients with VUR, 110 with RN (determined by absence/presence of renal scarring on dimercaptosuccinc acid scan), 27 with chronic renal failure due to RN, and 40 patients (control group) with urinary tract infection and normal findings on renal ultrasonography and voiding cystoureterogram. The ACE I/D, angiotensin II type 1 receptor AT1 A1166C, angiotensin II type 2 receptor A3123C AT2, and angiotensinogen AGT M235T polymorphisms were determined on the basis of polymerase chain reaction amplification. ACE serum levels were determined by spectrophotometric methods. We found no statistical differences in the distribution of RAS polymorphisms between the different groups. The ACE D allele was linked to higher ACE serum levels. We found no association between ACE I/D polymorphism and presence of hypertension, proteinuria, grade of VUR, or unilateral/bilateral VUR. Patients with the DD genotype had a lower incidence of febrile urinary tract infection as a first symptom of VUR/RN (P<0.05). We conclude that genetic polymorphisms of RAS components are not independent prognostic indicators of renal scarring in patients with VUR.


Subject(s)
Kidney Diseases/genetics , Renin-Angiotensin System/genetics , Vesico-Ureteral Reflux/genetics , Adolescent , Adult , Child , Child, Preschool , Gene Deletion , Humans , Infant , Kidney Failure, Chronic/genetics , Male , Mutagenesis, Insertional , Peptidyl-Dipeptidase A/genetics , Polymorphism, Genetic , Urinary Tract Infections/genetics
4.
J Trace Elem Med Biol ; 17(3): 171-6, 2003.
Article in English | MEDLINE | ID: mdl-14968929

ABSTRACT

Epidemiological evidence has raised concern that a moderate elevation in body iron stores may increase oxidative stress and risk of heart disease. We examined the cross-sectional association between plasma iron and factors that could affect its levels (antioxidant enzymes, diet), with the concentration of plasma malondialdehyde (MDA) as a marker of lipid peroxidation. Participants were 162 non-smoking institutionalised elderly. Our results show that those in the highest tertile of plasma iron were at least twice as likely to have higher plasma MDA levels. Among the factors affecting plasma iron levels, we found that the upper tertile of erythrocyte-superoxide dismutase (E-SOD) was inversely associated with higher plasma iron, and potato intake explained a sizeable proportion of the variation in plasma iron levels. In addition to potatoes, eggs, wine, fruit in men and green vegetables in women showed a positive association with plasma iron levels. Only potatoes in both sexes, wine in men and eggs in women had an independent effect on plasma MDA. Potatoes, wine, plasma lycopene and plasma iron accounted for 43% of the variability in plasma MDA for males, and E-SOD, potatoes, eggs, plasma lycopene and plasma iron explained 45% for women. A longitudinal study should confirm, whether these MDA levels are related to morbidity and mortality.


Subject(s)
Iron/blood , Lipid Peroxidation , Malondialdehyde/analysis , Malondialdehyde/blood , Aged , Female , Humans , Male , Odds Ratio , Regression Analysis
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