URINARY EXCRETION OF 17-HYDROXY-CORTICOSTEROIDS AND 17-KETOSTEROIDS IN HEALTHY SUBJECTS, IN RELATION TO SEX, AGE, BODY WEIGHT AND HEIGHT

1957 ◽  
Vol 25 (1) ◽  
pp. 33-44 ◽  
Author(s):  
R. Borth ◽  
A. Linder ◽  
A. Riondel
Keyword(s):  
Body Weight ◽  
Urinary Excretion ◽  
Healthy Subjects

Tryptophan-Niacin Metabolism in Rat with Puromycin Aminonucleoside-Induced Nephrosis

2006 ◽  
Vol 76 (1) ◽  
pp. 28-33 ◽  
Author(s):  
Yukari Egashira ◽  
Shin Nagaki ◽  
Hiroo Sanada
Keyword(s):  
Body Weight ◽  
Urinary Excretion ◽  
Enzyme Activities ◽  
Treated Group ◽  
Control Group ◽  
Puromycin Aminonucleoside ◽  
Low Level ◽  
Key Enzyme

We investigated the change of tryptophan-niacin metabolism in rats with puromycin aminonucleoside PAN-induced nephrosis, the mechanisms responsible for their change of urinary excretion of nicotinamide and its metabolites, and the role of the kidney in tryptophan-niacin conversion. PAN-treated rats were intraperitoneally injected once with a 1.0% (w/v) solution of PAN at a dose of 100 mg/kg body weight. The collection of 24-hour urine was conducted 8 days after PAN injection. Daily urinary excretion of nicotinamide and its metabolites, liver and blood NAD, and key enzyme activities of tryptophan-niacin metabolism were determined. In PAN-treated rats, the sum of urinary excretion of nicotinamide and its metabolites was significantly lower compared with controls. The kidneyα-amino-β-carboxymuconate-ε-semialdehyde decarboxylase (ACMSD) activity in the PAN-treated group was significantly decreased by 50%, compared with the control group. Although kidney ACMSD activity was reduced, the conversion of tryptophan to niacin tended to be lower in the PAN-treated rats. A decrease in urinary excretion of niacin and the conversion of tryptophan to niacin in nephrotic rats may contribute to a low level of blood tryptophan. The role of kidney ACMSD activity may be minimal concerning tryptophan-niacin conversion under this experimental condition.

Increased Urinary Excretion of Carnitine and Acylcarnitine by Mercuric Chloride Is Reversed by 2,3-Dimercapto-1-Propanesulfonic Acid in Rats

2010 ◽  
Vol 29 (3) ◽  
pp. 313-317
Author(s):  
Waleed A. Al-Madani ◽  
Nikhat J. Siddiqi ◽  
Abdullah S. Alhomida ◽  
Haseeb A. Khan ◽  
Ibrahim A. Arif ◽  
...  
Keyword(s):  
Body Weight ◽  
Urinary Excretion ◽  
Mercuric Chloride ◽  
Free Carnitine ◽  
Male Rats ◽  
Significant Protection ◽  
Total Carnitine ◽  
Dose Dependent Increase ◽  
Dose Dependent ◽  
Wistar Male Rats

This investigation was aimed to study the effect of 2,3-dimercapto-1-propanesulfonic acid (DMPS) on mercuric chloride (HgCl2)-induced alterations in urinary excretion of various carnitine fractions including free carnitine (FC), acylcarnitine (AC), and total carnitine (TC). Different groups of Wistar male rats were treated with HgCl2 at the doses of 0.1, 0.5, 1.0, 2.0, and 3.0 mg/kg body weight, and the animals were sacrificed at 24 hours following HgCl2 injection. A separate batch of animals received HgCl2 (2 mg/kg) with or without DMPS (100 mg/kg) and sacrificed at 24 or 48 hours after dosing. Administration of HgCl2 resulted in statistically significant and dose-dependent increase in the urinary excretion of FC, AC, and TC in rats. However, the ratio of urinary AC:FC was significantly decreased by HgCl2. Pretreatment with DMPS offered statistically significant protection against HgCl2-induced alterations in various urinary carnitine fractions in rats.

Effects of Protein Meals on the Urinary Excretion of Various Plasma Proteins in Healthy Subjects

Nephron ◽  
1999 ◽  
Vol 81 (4) ◽  
pp. 398-405 ◽  
Author(s):  
Takuma Narita ◽  
Hiroji Kitazato ◽  
Jun Koshimura ◽  
Katsunori Suzuki ◽  
Masahiko Murata ◽  
...  
Keyword(s):  
Urinary Excretion ◽  
Healthy Subjects ◽  
Plasma Proteins

scholarly journals Glucose-Induced Insulin Hypersecretion in Lipid-Infused Healthy Subjects Is Associated with a Decrease in Plasma Norepinephrine Concentration and Urinary Excretion

2001 ◽  
Vol 86 (10) ◽  
pp. 4901-4907 ◽  
Author(s):  
Christophe Magnan ◽  
Céline Cruciani ◽  
Laurence Clément ◽  
Pierre Adnot ◽  
Mylène Vincent ◽  
...  
Keyword(s):  
Insulin Secretion ◽  
Urinary Excretion ◽  
Healthy Subjects ◽  
Plasma Concentrations ◽  
Sympathetic Tone ◽  
Plasma Norepinephrine ◽  
C Peptide ◽  
Lipid Infusion ◽  
Hyperglycemic Clamp ◽  
Glucose Injection

We investigated the effect of a 48 h triglyceride infusion on the subsequent insulin secretion in response to glucose in healthy men. We measured the variations in plasma concentration and urinary excretion of catecholamines as an indirect estimation of sympathetic tone. For 48 h, 20 volunteers received a triglyceride/heparin or a saline solution, separated by a 1-month interval. At time 48 h, insulin secretion in response to glucose was investigated by a single iv glucose injection (0.5 g/kg−1) followed by an hyperglycemic clamp (10 mg·kg−1·min−1, during 50 min). The triglyceride infusion resulted in a 3-fold elevation in plasma free fatty acids and an increase in insulin and C-peptide plasma concentrations (1.5- and 2.5-fold, respectively, P < 0.05), compared with saline. At time 48 h of lipid infusion, plasma norepinephrine (NE) concentration and urinary excretion levels were lowered compared with saline (plasma NE: 0.65 ± 0.08 vs. 0.42 ± 0.06 ng/ml, P < 0.05; urinary excretion: 800 ± 70 vs. 620 ± 25 nmol/24 h, P < 0.05). In response to glucose loading, insulin and C-peptide plasma concentrations were higher in lipid compared with saline infusion (plasma insulin: 600 ± 98 vs. 310 ± 45 pm, P < 0.05; plasma C-peptide 3.5 ± 0.2 vs. 1.7 ± 0.2 nm, P < 0.05). In conclusion, in healthy subjects, a 48-h lipid infusion induces basal hyperinsulinemia and exaggerated insulin secretion in response to glucose which may be partly related to a decrease in sympathetic tone.

THYROXINE METABOLISM IN DIABETIC RATS

1977 ◽  
Vol 86 (2) ◽  
pp. 336-343 ◽  
Author(s):  
A. A. Zaninovich ◽  
T. J. Brown ◽  
R. Boado ◽  
N. R. Bromage ◽  
A. J. Matty
Keyword(s):  
Body Weight ◽  
Urinary Excretion ◽  
Least Squares Method ◽  
Intraperitoneal Administration ◽  
Binding Activity ◽  
Diabetic Rats ◽  
Control Group ◽  
Metabolic Clearance ◽  
Distribution Space

ABSTRACT The metabolism of thyroxine (T4) was determined in untreated and in insulin-treated diabetic rats. The results were compared with those obtained in a control group. Male Wistar rats weighing approximately 200 g were made diabetic by the intraperitoneal administration of streptozotocin (6.5 mg/100 g body weight) and 17 of those with blood sugar levels above 500 mg/100 ml were studied. In addition, 11 insulin-treated diabetic and 18 control rats were investigated. All the animals were injected intravenously with a tracer dose of [125I]T4 (1 μCi and 0.015 μg). After this blood samples were obtained by cardiac puncture at 16, 24, 40 and 48 h. The 24-h urinary excretion of inorganic 125iodide was also determined. The parameters of T4 metabolism were obtained by the least squares method and by an extrapolation technique. In untreated diabetic rats the fractional T4 turnover was 4.4%h, the distribution space 36.7 ml/100 g body weight, metabolic clearance 1.57 ml/100 g/h and urinary clearance 0.33 ml/100 g/h. The 24-h urinary excretion of 125iodide was 21.3 % of the injected radioactivity. Of these values the distribution space (P < 0.001) and metabolic clearance (P < 0.05) were significantly increased above those in the control animals. In insulin-treated rats all parameters were within normal values. Among these groups the serum T4 concentration was measured in 6 control, 5 untreated diabetic and 6 insulin-treated animals. The untreated diabetic animals had a significantly decreased serum T4 level but this was balanced by an enlarged distribution space so that the final hormone degradation was normal. In addition, the T4 binding activity of serum was assessed by the in vitro red cells uptake of [125I] T4 and by determining the proportion of serum free T4. Both these indices indicated a decrease in serum binding activity in the diabetic animals. The data suggest that the fall in serum T4 levels observed in the untreated diabetic rats was the result of decreased plasma binding of T4 and an increase in distribution space precipitated by lack of insulin.

Thin-layer chromatographic determination of urinary excretion of lactulose, simplified and applied to cystic fibrosis patients.

1987 ◽  
Vol 33 (7) ◽  
pp. 1211-1212 ◽  
Author(s):  
J A Flick ◽  
R L Schnaar ◽  
J A Perman
Keyword(s):  
Cystic Fibrosis ◽  
Oral Administration ◽  
Thin Layer ◽  
Urinary Excretion ◽  
Healthy Subjects ◽  
Chromatographic Determination ◽  
Solvent System ◽  
Chromatographic Technique ◽  
High Reproducibility

Abstract Urinary excretion of orally administered lactulose is used as an index of intestinal permeability. We have developed a simple thin-layer chromatographic technique for measuring lactulose in urine, using silica gel 60 plates and a propanol-borate solvent system. Lactulose concentrations as low as 62.5 mg/L can be detected with high reproducibility and without interference by urinary chromogens. After oral administration, the urinary excretion of lactulose in 8 h equaled 2.33 (SD 1.86)% in 15 patients with cystic fibrosis, as compared with 0.13 (SD 0.12)% in 16 healthy subjects (P less than 0.001).

The Effect of Mental Stress on Catecholamines, their Metabolites and Plasma Renin Activity in Patients with Essential Hypertension and in Healthy Subjects

1979 ◽  
Vol 57 (s5) ◽  
pp. 229s-231s ◽  
Author(s):  
W. Januszewicz ◽  
M. Sznajderman ◽  
B. Wocial ◽  
T. Feltynowski ◽  
T. Klonowicz
Keyword(s):  
Essential Hypertension ◽  
Plasma Renin Activity ◽  
Urinary Excretion ◽  
Mental Stress ◽  
Healthy Subjects ◽  
Plasma Renin ◽  
Renin Activity ◽  
Vanillylmandelic Acid ◽  
Before And After ◽  
Noradrenaline And Adrenaline

1. Ten patients with essential hypertension and ten healthy men were submitted to mental stress consisting of Kraepelin's arithmetic test combined with noise. Concentrations of plasma and urine catecholamines and of their metabolites as well as plasma renin activity before and after the test were studied. 2. In both groups a significant increase of noradrenaline and adrenaline in blood and noradrenaline in urine was observed. The urinary excretion of dopamine fell significantly in both groups after stress. 3. After mental stress a significant increase in urinary excretion of 3-methoxy-4-hydroxyphenylglycol was observed in both groups. The excretion of vanillylmandelic acid decreased significantly only in healthy subjects. 4. The plasma renin activity rose significantly in both groups but the increase was more pronounced in healthy subjects.

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