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1.
Am J Physiol ; 273(1 Pt 1): E17-27, 1997 Jul.
Article in English | MEDLINE | ID: mdl-9252475

ABSTRACT

To understand the mechanism of hepatic glycogen depletion found in uremia and under sucrose feeding, we examined net hepatic glycogenolysis-associated active enzymes and metabolites during fasting. Liver was taken 2, 7, and 18 h after food removal in uremic and pair-fed control rats fed either a sucrose or cornstarch diet for 21 days. Other uremic and control rats fasted for 18 h were refed a sucrose meal to measure glycogen increment. Glycogen storage in uremia was normal, suggesting effective glycogen synthesis. During a short fast, sucrose feeding and uremia enhanced net glycogenolysis through different but additive mechanisms. Under sucrose feeding, there were high phosphorylase alpha levels associated with hepatic insulin resistance. In uremia, phosphorylase alpha levels were low, but the enzyme was probably activated in vivo by a fall of inhibitors (ATP, alpha-glycerophosphate, fructose-1,6-diphosphate, and glucose) and a rise of Pi, as verified in vitro. Enhanced gluconeogenesis was also suggested, but excessive hepatic glucose production was unlikely in uremia. During fasting, hypoglycemia occurred in uremia due to reduced glycogenolysis, inefficient hepatic gluconeogenesis, and impaired renal gluconeogenesis. This may be relevant to poor fasting tolerance in uremia, which could be aggravated under excessive sucrose intake.


Subject(s)
Dietary Sucrose/pharmacology , Liver Glycogen/metabolism , Liver/metabolism , Phosphorylase a/metabolism , Uremia/metabolism , Animals , Blood Glucose/metabolism , Creatinine/blood , Dietary Carbohydrates , Glycogen Synthase/metabolism , Kidney/physiology , Kidney/physiopathology , Liver/anatomy & histology , Liver/drug effects , Male , Organ Size , Rats , Rats, Sprague-Dawley , Reference Values , Starch , Time Factors , Urea/blood , Weight Gain
2.
Kidney Int ; 52(6): 1550-60, 1997 Dec.
Article in English | MEDLINE | ID: mdl-9407500

ABSTRACT

Few studies have examined tubular function after subtotal nephrectomy (Nx) and conservative treatments. The effects of 70% and 80% Nx (associated with dietary phosphate restriction in the latter case) on the apical brush border membrane (BBM) enzymes 5'-nucleotidase, gamma glutamyl-transferase and alkaline-phosphatase, and one BBM Na-phosphate cotransporter (NaPi-2) were studied in rats after a six week period. Changes in activity and mRNA abundance of the BBM enzymes and in NaPi-2 protein and mRNA abundance were compared with changes in the distal markers of Na,K-ATPase activity and epidermal growth factor (EGF) production. The activity, but not the mRNA of BBM enzymes, was moderately reduced by the 70% Nx. Both the mRNA and activity of gamma glutamyl-transferase and alkaline-phosphatase were decreased in the 80% Nx, and the NaPi-2 mRNA, protein and Na,K-ATPase activities were also reduced. These effects (except for 5'nucleotidase and Na,K-ATPase) were partly reversed by phosphate restriction. Overproduction of EGF occurred after the 70% Nx, was blunted in the 80% Nx, and then partially restored by phosphate restriction. Aggravation of tubular alteration was associated with enhanced renal hyperplasia (increased DNA mass), reduced GFR and hyperphosphatemia, and high PTH levels, but reduced cAMP excretion. Improvement following phosphate restriction was associated with reduced hyperplasia and lowering of phosphatemia and PTH levels. These data demonstrate that Nx selectively affected BBM function through transcriptional changes that were partially reversed by phosphate restriction. Regulatory factors involved in these changes may include intracellular phosphate content and growth factors, but not the PTH effects that are impaired in chronic renal failure.


Subject(s)
Kidney Tubules/physiology , Kidney Tubules/surgery , Nephrectomy , Phosphorus, Dietary/pharmacology , Symporters , 5'-Nucleotidase/genetics , 5'-Nucleotidase/metabolism , Animals , Calcium/blood , Carrier Proteins/genetics , Carrier Proteins/metabolism , Cholecalciferol/blood , Epidermal Growth Factor/biosynthesis , Epidermal Growth Factor/metabolism , Gene Expression Regulation, Enzymologic/drug effects , Kidney Function Tests , Male , Membrane Proteins/metabolism , Microvilli/chemistry , Microvilli/drug effects , Microvilli/enzymology , Organ Size , Organ Specificity , Parathyroid Hormone/blood , Phosphates/blood , Phosphates/urine , RNA, Messenger/analysis , Rats , Rats, Sprague-Dawley , Sodium-Phosphate Cotransporter Proteins , Sodium-Potassium-Exchanging ATPase/metabolism , gamma-Glutamyltransferase/genetics , gamma-Glutamyltransferase/metabolism
3.
Clin Nephrol ; 46(1): 72-6, 1996 Jul.
Article in English | MEDLINE | ID: mdl-8832158

ABSTRACT

The effects of rhGH (H) daily injection (2 IU/d) and of vehicle (V) during two weeks were studied in young (60 g) growing rats. Experiment I was performed in uremic rats (mean plasma creatinine: 65-71 mumol/l) either acidotic (mean HCO3-:11.5 mmol/l: UAH, n = 20; UAV, n = 18), or with corrected acidosis by addition of NaHCO3 in the diet (mean HCO3-:26 mmol/l: UBH, n = 25; UBV, n = 23). Experiment II used rats with normal renal function (plasma creatinine: 25 mumol/l), either non-acidotic but food restricted to the dietary intake of uremic rats (CRH: n = 18, CRV: n = 18), or rendered acidotic by NH4Cl (CAH: n = 16, CAV: n = 16). GH induced an augmentation of body weight and length gains in non-acidotic uremic rats (+33% and +41%: p < 0.01), and in non-acidotic food restricted rats (+13% and 42%: p < 0.05 and p < 0.0001). This was associated with increased protein synthesis rate in muscle and with little change of food intake as well as of plasma IGF 1. Plasma IGF 1 kept the same relationship to food intake, regardless of treatment, but length gain for each level of plasma IGF 1 was enhanced by GH in GH responding groups. In both acidotic rat groups, GH altered none of the parameters studied. Thus: 1) the presence of severe metabolic acidosis blunts the response to GH in uremic and non-uremic rats. 2) The increment of growth rate does not depend on a rise of plasma IGF 1.


Subject(s)
Acidosis/drug therapy , Carbohydrates/blood , Human Growth Hormone/therapeutic use , Muscle Proteins/biosynthesis , Uremia/drug therapy , Acidosis/metabolism , Animals , Creatinine/blood , Diet , Disease Models, Animal , Hydrogen-Ion Concentration , Insulin-Like Growth Factor I/metabolism , Male , Rats , Rats, Sprague-Dawley , Recombinant Proteins , Urea/blood , Uremia/metabolism
4.
Am J Physiol ; 270(6 Pt 2): F997-1003, 1996 Jun.
Article in English | MEDLINE | ID: mdl-8764319

ABSTRACT

Tubular overwork is thought to be a promoter of the tubular hypertrophy and renal failure that occur in response to renal mass reduction. Because Na-K-adenosinetriphosphatase (Na-K-ATPase) is an index of tubular work, we evaluated the effects of subtotal nephrectomy and of enalapril therapy, which delays the evolution of renal lesions, on tubular hypertrophy and Na-K-ATPase activity along the rat nephron. Within 6 wk, 70% reduction of renal mass engendered hypertrophy of the proximal convoluted tubule (PCT), thick ascending limb (TAL), and collecting duct (CD), as well as parallel increments in Na-K-ATPase activity per millimeter tubule length (Na-K-ATPase activity per unit surface area was not modified by subtotal nephrectomy). Chronic enalapril therapy prevented part of the hypertrophy (but not Na-K-ATPase stimulation) of the PCT and the whole stimulation of Na-K-ATPase (but not hypertrophy) in the CD, whereas it had no effect on the TAL. Enalapril effect on Na-K-ATPase in CD might result from reduced bradykinin metabolism, as the reduction in urinary excretion of bradykinin observed in subtotally nephrectomized rats was prevented by enalapril therapy.


Subject(s)
Enalapril/pharmacology , Nephrectomy , Nephrons/enzymology , Sodium-Potassium-Exchanging ATPase/metabolism , Aldosterone/blood , Animals , Bradykinin/urine , Hypertrophy/prevention & control , Kidney Tubules/drug effects , Kidney Tubules/enzymology , Kidney Tubules/pathology , Male , Rats , Rats, Wistar
5.
Pediatr Nephrol ; 10(3): 256-60, 1996 Jun.
Article in English | MEDLINE | ID: mdl-8792385

ABSTRACT

The effects of 2 weeks of a daily injection (2 IU/day) of recombinant human growth hormone (GH) were studied in young (60-g) growing rats in two experiments. Experiment 1 was performed in uremic animals (mean plasma creatinine 65-71 mumol/l) who were either acidotic (mean bicarbonate 11.5 mmol/l) or had acidosis corrected (mean bicarbonate 26 mmol/l) by addition of sodium bicarbonate to the diet. Experiment 2 used rats with normal renal function (plasma creatinine 25 mumol/l) who were either non-acidotic but restricted to the dietary intake of uremic rats or rendered acidotic by ammonium chloride. GH induced an increase in body weight and length in non-acidotic uremic (+33% and +41%) and in non-acidotic food-restricted (+13% and +42%) rats, associated with an increased rate of protein synthesis and little change in plasma insulin-like growth factor 1 (IGF 1). In both acidotic rat groups, GH altered none of the parameters studied. Thus: (1) the presence of severe metabolic acidosis blunts the response to GH in uremic and non-uremic rats and (2) the increment of growth rate does not depend on a rise in plasma IGF 1.


Subject(s)
Acidosis/physiopathology , Growth Hormone/pharmacology , Growth/physiology , Uremia/physiopathology , Acidosis/complications , Ammonium Chloride/pharmacology , Animals , Carbon Dioxide/blood , Diet , Growth/drug effects , Humans , Insulin-Like Growth Factor I/metabolism , Male , Nephrectomy , Oxygen/blood , Rats , Rats, Sprague-Dawley , Sodium Bicarbonate/pharmacology , Uremia/complications
6.
Miner Electrolyte Metab ; 22(1-3): 88-91, 1996.
Article in English | MEDLINE | ID: mdl-8676834

ABSTRACT

Because of constant uremia-induced anorexia, food restriction of normal rats is generally used to study the consequences of uremia. The effects of a normal food supply in uremic rats has never been tested, since no author has succeeded in providing normal intakes. Uremic rats either fed ad lib (U rats, n = 12) or force-fed through a gastric catheter (UF rats, n = 10), and sham-operated rats (C rats, n = 10) were compared from days 7 to 21 after surgery. U rats had lower food intake (13.8 vs. 17 g/day), weight gain (5.16 vs. 6.23 g/day), length gain (4 vs. 5 mm/day), nitrogen balance (228 vs. 279 mg/day) and muscle fractional protein synthesis rate (9.5 vs. 10.6%) measured in vivo by 3H-phenylalanine injection (p < 0.05 for all). All parameters were restored to normal values in UF rats, possibly due to correction of underhydration in addition to undernutrition. Such continuous enteral feeding may provide a model for normal nutritional supply in uremia.


Subject(s)
Enteral Nutrition , Uremia/physiopathology , Animals , Anorexia/etiology , Bicarbonates/blood , Blood Proteins/metabolism , Calcium/blood , Creatinine/blood , Feeding Behavior , Male , Muscle, Skeletal/metabolism , Phosphates/blood , Protein Biosynthesis , Rats , Rats, Sprague-Dawley , Reference Values , Sodium/blood , Urea/blood , Uremia/blood , Uremia/therapy , Weight Gain
8.
Am J Physiol ; 268(5 Pt 2): F793-801, 1995 May.
Article in English | MEDLINE | ID: mdl-7539585

ABSTRACT

It is generally accepted that renal compensatory growth after unilateral nephrectomy (Uni) is due to prominent hypertrophy with no involvement of protooncogenes. Neither the balance between hypertrophy and hyperplasia nor the expression of the early-growth-related genes has been studied after subtotal nephrectomy (Nx). The occurrence of cystic tubular dilatations after Nx may suggest an excessive cell proliferation in this model. We measured DNA, RNA, and protein content, number of nuclei per tubular section, as well as c-fos, c-jun, c-myc, c-H-ras, c-sis, and c-erb-B2 protooncogene expression in kidneys taken at time of surgery and 2, 7, and 14 days after sham operation (control rats), Uni, or Nx. After Uni, hyperplasia was greater than expected (+79% for DNA at day 14) and was associated with moderate hypertrophy (+11% for protein/DNA ratio). After Nx, compensatory growth was due only to hyperplasia (+117% for DNA at day 14), with unchanged protein/DNA ratio (vs. Uni, P < 0.02). The greater hyperplasia after Nx was confirmed by nuclei counting. The protooncogene mRNA expression was constantly absent in control and Uni rats, whereas that of c-fos and c-jun genes was detected in Nx rats at day 14 with a 2- to 12-fold increment. The c-fos and c-jun protein levels were also increased at that time in Nx rats. This suggests the following: 1) the cellular events following Uni and Nx are not the same, and 2) the late protooncogene expression in Nx exclusively could favor a particular type of cell proliferation possibly more related with cystic formation than with actual compensatory growth.


Subject(s)
Gene Expression , Kidney/pathology , Kidney/physiopathology , Nephrectomy/methods , Proto-Oncogenes , Adaptation, Physiological , Animals , DNA/metabolism , Hyperplasia , Male , Proto-Oncogene Proteins/metabolism , RNA/metabolism , RNA, Messenger/metabolism , Rats , Rats, Wistar
9.
Nephrologie ; 16(2): 203-8, 1995.
Article in French | MEDLINE | ID: mdl-7753304

ABSTRACT

Children with chronic renal failure (CRF) show a reduced appetite for sweet foods. Sensory responses to sweet stimuli were investigated in 45 children with CRF, 39 dialyzed patients (HD) and 25 controls(C). Two familiar foods were prepared in 5 sucrose concentrations: 1, 5, 10, 15, 20% for soft white cheese (SWC): 10, 20, 30, 40, 60% for apple sauce (AS). When identifying the sweeter of two SWC samples, CRF(15%) and HD (18%) made more mistakes than C (5%). When testing AS, mistakes were comparable between groups (25, 21, 19%). Preferences differed according to diagnosis group. The sweetest SWC was preferred by 40% of CRF and C and by only 22% HD; the least sweet SWC was preferred by 5% of C, 10% of CRF and 16% of HD. In AS, the highest concentrations were preferred by CRF and C, median concentration by HD. Plasma zinc had no clear effect on taste. Altered preferences for sweet foods in patients suggest post-ingestive adverse effects of sucrose resulting from an altered sucrose metabolism.


Subject(s)
Food Preferences , Kidney Failure, Chronic/physiopathology , Sucrose , Taste , Adolescent , Child , Child, Preschool , Female , Humans , Male , Renal Dialysis , Zinc/blood
11.
Kidney Int ; 46(6): 1705-12, 1994 Dec.
Article in English | MEDLINE | ID: mdl-7700030

ABSTRACT

Chronic metabolic acidosis (CMA) is a major cause of growth defect, implying disturbances of protein metabolism. Previously, in vivo studies performed in the fasting state showed enhanced whole body protein turnover, whereas in vitro studies showed unchanged muscle protein synthesis. The present study is the first to determine the effects of CMA on muscle protein synthesis and degradation in vivo. Two studies were performed in 60 g male rats fed a 30% casein diet. In study I, one group was sham-operated (C rats), and two groups underwent subtotal nephrectomy. One of them developed acidosis (UA rats) which was corrected in the other by NaHCO3 in the diet (UNA rats). Study II compared sham-operated rats rendered acidotic by NH4Cl in the drinking water (CA rats) and normal pair-fed (CNA) rats. Fractional protein synthesis rate (FSR) was determined in gastrocnemius muscle after injection of 3H-phenylalanine. Fractional protein degradation rate (FDR) was calculated as FSR minus fractional rate of muscle growth (FGR). In study I, UA rats had lower growth and N balance (163 +/- 12 vs. 216 +/- 11 mg N/day; P < 0.001) than UNA rats, despite identical food intake (11 g/day). This was associated with identical FSR (10.4 +/- 0.5 vs. 10.9 +/- 0.5%/day), but enhanced protein degradation (6.30 +/- 0.99 vs. 5.10 +/- 0.71%/day; P < 0.05). Plasma insulin, C peptide, PTH and corticosterone did not differ in UA and UNA rats, whereas plasma IGF-I was markedly reduced (147 +/- 21 vs. 283 +/- 27 ng/ml; P < 0.01) in UA rats.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Acidosis/metabolism , Muscle Proteins/biosynthesis , Acidosis/etiology , Animals , Chronic Disease , Corticosterone/blood , Disease Models, Animal , Growth Disorders/etiology , Insulin/blood , Insulin-Like Growth Factor I/metabolism , Kinetics , Male , Rats , Rats, Sprague-Dawley , Uremia/complications
12.
Am J Physiol ; 266(5 Pt 2): F746-55, 1994 May.
Article in English | MEDLINE | ID: mdl-8203558

ABSTRACT

Inulin clearance (CIn) was measured in the presence of varying degrees of renal excision (NX, 0-85% of renal mass by weight), in anesthetized rats fed on high-protein (HP, 30%), median-protein (MP, 10%), or low-protein (LP, 7%) diets, before and during amino acid (AA) infusion or before and after an intragastric protein load. CIn was higher in rats fed HP than in rats fed LP in controls (3.4 vs. 2.1 ml/min) and in rats with NX up to 70% after feeding for 3 wk (1.4 vs. 0.7 ml/min) or 4 days (1.5 vs. 1.1 ml/min). The difference decreased from 0% to 70% NX, and disappeared when NX exceeded 70%. Acute AA infusion and intragastric loads always increased CIn with wide individual variations. The increase was greater in rats fed HP than in rats fed MP and LP (+1.4 vs. 0.8 and 1.1 ml/min for 0% NX), diminished with greater NX (0.7 vs. 0.2 and 0.4 ml/min for 70% NX), and was very small for NX above 70%. However, when expressed as the percent of baseline values, the mean CIn increment after acute stimulation remained constant (30-45%), regardless of renal ablation and of diet. Thus preexisting hyperfiltration resulting from diet or from renal ablation does not suppress the glomerular response to an acute protein load, and acute loads afford no advantages over baseline glomerular filtration rate (GFR) measurements. By contrast, chronic protein feeding increases GFR only when nephron loss is not too severe.


Subject(s)
Amino Acids/pharmacology , Dietary Proteins , Glomerular Filtration Rate , Kidney Glomerulus/physiology , Nephrons/physiology , Amino Acids/administration & dosage , Animals , Blood Pressure , Creatinine/blood , Glomerular Filtration Rate/drug effects , Hematocrit , Infusions, Intravenous , Inulin , Kidney Glomerulus/drug effects , Male , Nephrons/drug effects , Rats , Rats, Sprague-Dawley , Reference Values
13.
Metabolism ; 43(4): 403-12, 1994 Apr.
Article in English | MEDLINE | ID: mdl-8159094

ABSTRACT

A high-sucrose (S) diet accentuates anorexia and stunts growth in uremic (U) rats, and an oral S load induces a greater hyperfructosemia in U rats than in control (C) rats. Four studies were performed to determine the roles of S feeding and an acute S load on liver carbohydrate (CHO) metabolism in U and C rats (eight to 10 rats per group). We also examined the plasma responses to either water or a S load. Levels of the main metabolites of glycolysis, gluconeogenesis, and glycogenesis were measured under basal conditions (7 hours' postmeal) in U and C rats fed either a cornstarch diet (study I) or S diet (study II) and at 30 and 60 minutes after an intragastric S load (studies III and IV) in s-fed U and C rats. The weight gain, food intake, and plasma creatinine and urea levels of the rats in the four studies were comparable. Weight gain and liver weight (g/100 g body weight) were lower in U than in C rats. In the plasma, baseline levels of lactate were decreased by uremia and S feeding and those of glucose (G) were increased by S feeding. The increases in plasma G and fructose (F) levels after a S load were greater in U rats than in C rats, whereas those of plasma lactate were comparable. In the liver under basal conditions, uremia markedly decreased levels of glycogen, F-1,6-diphosphate (F-1,6-diP), F-2,6-diP, 3-glycero-phosphate (3-glycero-P), dihydroxyacetone phosphate (DHAP), pyruvate, lactate, and adenosine triphosphate (ATP), and the phosphorylation state (ATP/adenosine diphosphate [ADP] x inorganic phosphorus [PI]), increased phosphoenolpyruvate (PEP), ADP, and Pi levels, but did not affect the cytosolic redox state (pyruvate/lactate). In addition to uremia, S feeding further decreased levels of glycogen, F-2,6-diP, 3-glycero-P, and ATP. After S loading, liver F levels increased more in U than in C rats, but glycogen and 3-glycero-P levels increased less in U than in C rats. Liver lactate and pyruvate levels increased more in U than in C rats, and the pyruvate/lactate and DHAP/3-glycero-P ratios were higher in U than in C rats after a S load. The ATP level and the phosphorylation state in U rats increased 30 minutes later in U than in C rats. Our findings indicate that uremia causes a depletion in liver glycogen, which is enhanced by S feeding and could be partially attributed to decreased glycogen synthesis.(ABSTRACT TRUNCATED AT 400 WORDS)


Subject(s)
Carbohydrate Metabolism , Glucose/metabolism , Liver/metabolism , Sucrose/pharmacology , Uremia/metabolism , Animals , Kidney/metabolism , Nutritional Status , Rats , Sucrose/administration & dosage , Uremia/blood
14.
Nat Genet ; 3(4): 342-5, 1993 Apr.
Article in English | MEDLINE | ID: mdl-7981755

ABSTRACT

Familial juvenile nephronophthisis (NPH) is a chronic autosomal recessive kidney disease responsible for 15% of end stage renal failure in children. NPH is frequently (16% of cases) associated with Leber amaurosis (termed Senior-Løken syndrome, SLS). Linkage analyses, performed in 22 multiplex NPH families (18 without and 4 with ocular abnormalities), have localized the gene to a region between D2S48 and D2S51 on chromosome 2p. This was confirmed using adjacent microsatellite markers, one of which (AFM220ze3 at the D2S160 locus) gave a lod score of 4.78 at theta = 0.05 in the 18 families with isolated NPH, whereas the same marker excluded linkage with SLS. These results demonstrate linkage of the purely renal form of NPH to chromosome 2p, and suggest that there may be genetic heterogeneity between NPH and SLS.


Subject(s)
Chromosomes, Human, Pair 2 , Kidney Diseases/genetics , Base Sequence , Child , Chromosome Mapping , Cloning, Molecular , DNA Primers , DNA, Satellite/genetics , Female , Genes, Recessive , Genetic Linkage , Humans , Kidney Failure, Chronic/etiology , Kidney Failure, Chronic/genetics , Lod Score , Male , Molecular Sequence Data , Pedigree , Polymerase Chain Reaction
15.
Ann Pediatr (Paris) ; 40(2): 90-4, 1993 Feb.
Article in French | MEDLINE | ID: mdl-8457137

ABSTRACT

Two studies of uremia-induced chronic metabolic acidosis (CMA) were carried out to determine: 1) the level of acidosis beyond which growth failure occurs; 2) the protein metabolism anomalies which are associated with growth failure. Rats rendered uremic by subtotal nephrectomy were fed a diet containing sufficient protein amounts (30% casein) to induce CMA. CMA was left uncorrected in half the rats (group A) and was corrected by administration of bicarbonate in the other half (group B). 1) Fifty-two group A rats were compared with 52 group B rats matched for renal function. Results showed that a) CMA failed to reduce food intake; b) weight gain decreased only when CMA was profound (pH < 7.20) whereas reductions in length gain occurred at less severe levels of acidosis (pH < 7.25) suggesting that bone may be more susceptible to CMA than muscle mass. 2) Protein fractional synthesis rate was evaluated in skeletal muscle after a flooding dose of 3H-phenylalanine in group A rats (pH 7.22 +/- 0.01, HCO3-: 15.2 +/- 0.8 mmol/l) and group B rats matched for renal function. Values were identical in both groups (10.4 +/- 0.5 vs 10.8 +/- 0.5%/day). However, fractional muscle protein accretion rate was decreased in group A rats. These data demonstrate that CMA-associated growth failure in uremia is due to increased breakdown of protein with no change in protein production.


Subject(s)
Acidosis, Lactic/metabolism , Growth Disorders/etiology , Muscles/metabolism , Proteins/metabolism , Renal Insufficiency/complications , Acidosis, Lactic/etiology , Acidosis, Lactic/physiopathology , Animals , Disease Models, Animal , Eating , Growth Disorders/diagnosis , Kidney Function Tests , Male , Protein Biosynthesis , Rats , Rats, Sprague-Dawley , Renal Insufficiency/diagnosis , Weight Gain
16.
Exp Nephrol ; 1(1): 62-4, 1993.
Article in English | MEDLINE | ID: mdl-7521767

ABSTRACT

Renal clearance of endogenous 5-HIAA has been shown to be similar to that of PAH in humans. The present study compared 5-HIAA and PAH clearances in rats. It showed that the clearance of 5-HIAA in rats was identical to that of inulin and creatinine. This suggests that in this species, 5-HIAA is only filtered and not secreted by the tubules in contrast to what is observed in humans.


Subject(s)
Hydroxyindoleacetic Acid/pharmacokinetics , Kidney/metabolism , Animals , Biomarkers , Humans , Hydroxyindoleacetic Acid/blood , Kidney Tubules/metabolism , Male , Metabolic Clearance Rate , Rats , Rats, Sprague-Dawley , Renal Circulation/physiology , Species Specificity , p-Aminohippuric Acid/blood , p-Aminohippuric Acid/pharmacokinetics
17.
Am J Clin Nutr ; 56(6): 1025-33, 1992 Dec.
Article in English | MEDLINE | ID: mdl-1442653

ABSTRACT

Insufficient protein diets supplemented with ketoanalogue/essential amino acid (KA/EAA) mixtures are proposed to maintain nutrition and to retard renal deterioration. We compared in growing and in adult uremic rats diets containing limited or usual amounts of protein (12%, 20% for growing rats, and 10% and 16% for adult rats) with diets containing 50% or 60% less casein plus a KA/EAA mixture providing KA at an equimolar amount of removed EAA or at higher amounts. The latter supplement caused stunting, the former caused no anorexia, a slight growth deficit when added to the lowest basal casein diets, and almost normal growth when added to higher casein diets. Growth was normal with EAA supplements. The plasma EAA changes were unrelated to intake and to growth. Thus, KA utilization is maximal, provided that basal protein is sufficient and KA are not in excess.


Subject(s)
Amino Acids, Essential/therapeutic use , Animal Nutritional Physiological Phenomena , Diet , Keto Acids/therapeutic use , Uremia/diet therapy , Amino Acids, Branched-Chain/blood , Amino Acids, Essential/administration & dosage , Amino Acids, Essential/blood , Animals , Dietary Proteins/administration & dosage , Eating , Keto Acids/administration & dosage , Male , Nitrogen/metabolism , Rats , Rats, Sprague-Dawley , Urea/blood , Weight Gain
18.
J Lab Clin Med ; 120(6): 851-60, 1992 Dec.
Article in English | MEDLINE | ID: mdl-1453107

ABSTRACT

Low-protein diets supplemented with keto-analogues and essential amino acid (KA-EAA) mixtures or with EAA have been widely used to retard renal deterioration without affecting nutrition. These assumptions have recently been challenged in clinical studies and rest on little or no experimental data. The effects of EAA and KA-EAA supplementations have not been compared. We compared three groups of rats with subtotal nephrectomy that were fed (1) a 16% casein reference (R) diet, (2) a 6% casein plus EAA (A) diet, or (3) a 6% casein plus KA-EAA (K) diet with KA as amino acid salts. The three diets had the same energy and mineral contents, and they induced comparable growth. The two supplements had the same nitrogen content. The only difference found until month 3 was higher proteinuria and plasma urea levels in group R rats. Renal biopsies performed at month 3 showed more severe glomerular sclerosis and tubular changes in R rats than in A and K rats. From months 3 through 7, R rats developed higher plasma creatinine levels than did A and K rats (final median values: 167, 106, and 83 mumol/L; p < 0.04), had more proteinuria (232, 56, and 84 mg/day), and showed greater mortality rates. At the time the rats were killed, 2 R, 6 A, and 5 K rats had survived while receiving the diets. Examination of the remnant kidneys, regardless of time of death, showed that renal lesions were significantly worse in R than in A and K rats, with sclerosis affecting more than 50% of the glomeruli in 7 of 13 R, 4 of 14 A, and 4 of 15 K rats, and less than 25% glomeruli in 2 of 13 R, 10 of 14 A, and 10 of 15 K rats (A and K vs R: p < 0.03). In conclusion, restriction of nonessential amino acids compensated by EAA or by KA-EAA mixtures retards renal damage without affecting growth, but no real benefit of KA or EAA has been observed.


Subject(s)
Dietary Proteins/administration & dosage , Kidney/pathology , Nephrectomy/adverse effects , Nutrition Disorders/prevention & control , Amino Acids, Essential/pharmacology , Animals , Creatinine/blood , Kidney/physiology , Male , Rats , Rats, Sprague-Dawley
19.
Am J Pathol ; 141(6): 1481-9, 1992 Dec.
Article in English | MEDLINE | ID: mdl-1466405

ABSTRACT

Rats progressively develop proteinuria and glomerular sclerosis with age. These physiologic and histologic changes are accelerated by subtotal renal mass ablation. Alterations in the glomerular basement membrane (GBM), such as thickening and decreased anionic site density, occur during senescence. This study examines the ultrastructural alterations of the GBM affecting remnant glomeruli. Six week-old male Wistar rats underwent a subtotal nephrectomy (70%) and were compared with sham operated rats. Rats were fed a standard diet, and physiologic measurements were performed every 3 weeks. Rats were killed 6 and 12 weeks after surgery. Anionic sites were labeled by polyethyleneimine perfusion before killing. Kidneys were processed for light and electron microscopy. Nephrectomized rats had higher protein-uria than the controls and developed glomerular sclerosis. The GBM of nephrectomized rats were significantly thinner and anionic sites were less numerous 12 weeks after nephrectomy, especially in the lamina densa (LD) of the GBM. The number and distribution of anionic sites were similar to those observed in sham operated rats killed 6 weeks after surgery. These results indicate that glomerular sclerosis and GBM thickening are unrelated phenomena. They also suggest that the number and density of anionic sites in LD are not a prominent factor for increasing proteinuria after subtotal nephrectomy.


Subject(s)
Anions/analysis , Kidney Glomerulus/chemistry , Kidney Glomerulus/ultrastructure , Nephrectomy , Polyethyleneimine/analysis , Aging/pathology , Animals , Basement Membrane/chemistry , Basement Membrane/physiology , Basement Membrane/ultrastructure , Histocytochemistry , Kidney Glomerulus/pathology , Male , Microscopy, Electron , Rats , Rats, Wistar
20.
Kidney Int ; 42(2): 354-63, 1992 Aug.
Article in English | MEDLINE | ID: mdl-1405318

ABSTRACT

Angiotensin converting enzyme inhibitors (ACEI) are believed to protect remnant kidney, but all previous studies used the ligation model which causes severe hypertension, and very few have compared drugs in rats having similar control of blood pressure (BP). We compared rats with uremia obtained by 70% excision of total renal mass, a model which causes mild, late hypertension. Study I compared the effects of enalapril (E), cicletanine (C) and placebo (P) in uremic (U) rats fed a 0.50% (normal-high) Na diet. Study II compared the effects of E, C, P, and guanfacine (G) in U rats fed a diet restricted to 0.25% Na (normal-low). In study I, UP rats developed progressive hypertension (140, 146, 160 and 166 mm Hg at 3, 6, 9 and 12 weeks), proteinuria (240 mg/day at 9 and 12 weeks) which were not affected by E or C. The occurrence of end-stage renal disease (ESRD) led to the sacrifice of all rats after three months. All three groups had similar severe renal lesions (over 25% sclerosed glomeruli in 5 of 10 UP, 9 of 14 UE, 7 of 14 UC rats, with huge cystic tubular dilatations). In study II, rats could be sacrificed later (6 months) and had evidence of less severe renal disease. All the drugs tested prevented hypertension throughout the study (P less than 0.001), with lowest values in UE rats. E and G, but not C, reduced proteinuria. Renal damage was reduced with E and G, but not with C, despite similar BP in C and G rats. Thus, in contrast with what was obtained in the ligation model, ACEI affected neither the BP nor the renal lesions of rats made uremic by renal excision and fed a 0.50% Na diet. Moderate Na restriction improved the consequences of nephron loss and restored the anti-hypertensive effect of drugs. However, these drugs had a different effect on renal preservation: it was dramatic with E, good with G, and undetectable with C.


Subject(s)
Antihypertensive Agents/therapeutic use , Hypertension, Renal/drug therapy , Kidney/drug effects , Pyridines , Sodium, Dietary/administration & dosage , Animals , Disease Models, Animal , Diuretics/therapeutic use , Enalapril/therapeutic use , Hypertension, Renal/etiology , Hypertension, Renal/pathology , Kidney/pathology , Male , Nephrectomy , Rats , Rats, Wistar , Uremia/drug therapy , Uremia/etiology , Uremia/pathology
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