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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0009452,
umls-concept:C0013125,
umls-concept:C0025519,
umls-concept:C0026447,
umls-concept:C0031327,
umls-concept:C0034693,
umls-concept:C0040162,
umls-concept:C0205171,
umls-concept:C0205435,
umls-concept:C0221102,
umls-concept:C0243071,
umls-concept:C0377441,
umls-concept:C0683150,
umls-concept:C1280551
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pubmed:issue |
2
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pubmed:dateCreated |
1997-1-23
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pubmed:abstractText |
The plasma concentrations, metabolism and excretion were studied in rats, dogs and monkeys after a single intravenous administration of 14C-montirelin hydrate (CAS 90243-66-6, 14C-NS-3). 1. The plasma concentration of radioactivity and the area under curve (AUC0-infinity) increased with the dose after intravenous administration of 0.25, 1 and 4 mg/kg to male rats. 2. Until 4 h after intravenous administration of 0.25 mg/kg, the plasma concentration of radioactivity decreased with half-lives of 0.512, 0.771 and 0.786 h in male rats, dogs and monkeys, respectively. The plasma concentration of radioactivity in rats increased 6-10 h after administration, suggesting enterohepatic circulation. 3. The plasma concentration of NS-3 in various animal species decreased biphasically after intravenous administration. The elimination half-lives, t1/2 beta, in rats, dogs and monkeys were 0.324, 0.679 and 0.682 h, respectively, and the steady state volumes of distribution, Vdss, were 0.248, 0.319 and 0.306 l/kg, respectively. 4. The binding of NS-3 to serum protein was less than 3% in rats, dogs, monkeys and humans. 5. Within 48 h after intravenous administration of 1 mg/kg to male rats, the excretion of radioactivity in urine, feces and expired air was 67.3, 15.0 and 14.8% of the dose, respectively (total 97.1%). The biliary excretion of radioactivity was 26.6% within 24 h after dosing. 6. No sex-related difference was found in plasma concentration of radioactivity or the excretion of radioactivity in urine, feces and expired air after intravenous administration of 1 mg/kg to male and female rats. 7. In male dogs, the excretion of radioactivity in urine and feces was 92.3 and 5.6% of the dose, respectively, during 72 h after intravenous administration of 0.25 mg/kg (total 97.9%). 8. In male monkeys, the excretion of radioactivity in urine and feces was 91.7 and 2.9% of the dose, respectively, during 72 h after intravenous administration of 0.25 mg/kg (total 94.6%). 9. The urinary excretion of NS-3 and its main metabolite CNK-6004 (deamidation product) during 24 h after intravenous administration was 31.4 and 25.3% of the dose in male rats, 45.4 and 30.1% in male dogs, and 20.2 and 48.0% in male monkeys, respectively. The biliary excretion of NS-3 and CNK-6004 in male rats was 1.1 and 17.4%, respectively, during 24 h after administration. 10. The radioactivity in the bile collected from donor rats that had received 14C-NS-3 was easily absorbed from the intestinal tract of recipient rats after intraduodenal administration of the donor's bile.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0004-4172
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
46
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
106-13
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pubmed:dateRevised |
2005-11-17
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pubmed:meshHeading |
pubmed-meshheading:8720298-Animals,
pubmed-meshheading:8720298-Bile,
pubmed-meshheading:8720298-Chromatography, Thin Layer,
pubmed-meshheading:8720298-Dogs,
pubmed-meshheading:8720298-Enterohepatic Circulation,
pubmed-meshheading:8720298-Feces,
pubmed-meshheading:8720298-Female,
pubmed-meshheading:8720298-Humans,
pubmed-meshheading:8720298-Injections, Intravenous,
pubmed-meshheading:8720298-Macaca fascicularis,
pubmed-meshheading:8720298-Male,
pubmed-meshheading:8720298-Models, Biological,
pubmed-meshheading:8720298-Protein Binding,
pubmed-meshheading:8720298-Rats,
pubmed-meshheading:8720298-Rats, Sprague-Dawley,
pubmed-meshheading:8720298-Sex Characteristics,
pubmed-meshheading:8720298-Species Specificity,
pubmed-meshheading:8720298-Thyrotropin-Releasing Hormone
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pubmed:year |
1996
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pubmed:articleTitle |
Pharmacokinetics of the new thyrotropin releasing hormone analogue montirelin hydrate. 1st communication: plasma concentrations, metabolism and excretion after a single intravenous administration to rats, dogs and monkeys.
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pubmed:affiliation |
Research Laboratories, Nippon Shinyaku Co., Ltd., Kyoto, Japan.
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pubmed:publicationType |
Journal Article
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