Literature DB >> 135705

Streptozotocin: its excretion and metabolism in the rat.

E H Karunanayake, D J Hearse, G Mellows.   

Abstract

The excretion of radioisotope following the administration of three specifically 14C-labelled forms of streptozotocin was investigated in the rat using ureter and bile duct cannulation techniques. The urine collected during the first hour following the administration of the drug contained the highest proportion of injected radioactivity (approximately 34% with (3'-methyl-14C)-streptozotocin and approximately 40% each with (1-14C)-and (2'-14C)-streptozotocin. Over the entire experimental period (6 hours), approximately 70% of the injected radioactivity of (1-14C)- and (2'-14C)-streptozotocin appeared in the urine. With (3'-methyl-14C)-streptozotocin, only 53% of the injected radioactivity appeared in the urine over the same period. In contrast to the high urinary excretion, less than 3% of the injected radioactivity from all three radiolabelled streptozotocin samples appeared in the bile. The in vivo and in vitro metabolism of streptozotocin was also investigated. In addition to substantial amounts of unchanged drug, three radiolabelled metabolites (two major and one minor) were detected in the urine during the 6 hour collection period following the administration of (1-14C)- and (2'-14C)-streptozotocin. In contrast, only unchanged (3'-methyl-14C)-streptozotocin was detected in the urine collected over the same period following the administration of the methyl labelled drug. The two major metabolites were also produced when (1-14C)-and (2'-14C)-streptozotocin were incubated with a rat liver supernatant fraction (100,000 X g). The liver was further demonstrated to be the major site of metabolism in isolated liver perfusion studies in which both (1-14C)- and (2'-14C)-streptozotocin were quantitatively converted to the two major metabolites. The two major metabolites of (1-14C)-streptozotocin, whether produced in vivo or in vitro, were chromatographically homogenous with the two major metabolites formed from (2'-14C)-streptozotocin. Nicotinamide pretreatment had no apparent effect on the urinary excretion of streptozotocin and its metabolites.

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Year:  1976        PMID: 135705     DOI: 10.1007/bf01219512

Source DB:  PubMed          Journal:  Diabetologia        ISSN: 0012-186X            Impact factor:   10.122


  16 in total

1.  The metabolic fate and elimination of streptozotocin.

Authors:  E H Karunanayake; D J Hearse; G Mellows
Journal:  Biochem Soc Trans       Date:  1975       Impact factor: 5.407

2.  Microadioautographic study of the distribution and uptake of [14C] streptozotocin in rat tissue.

Authors:  E H Karunanayake; R J Baker; R Christian; D J Hearse; G Mellows
Journal:  Biochem Soc Trans       Date:  1975       Impact factor: 5.407

3.  The management of nicotinamide and nicotinic acid in the mouse.

Authors:  P B Collins; S Chaykin
Journal:  J Biol Chem       Date:  1972-02-10       Impact factor: 5.157

4.  Studies on the ability of compounds to block the diabetogenic activity of streptozotocin.

Authors:  W E Dulin; B M Wyse
Journal:  Diabetes       Date:  1969-07       Impact factor: 9.461

5.  Streptozotocin: depression of mouse liver pyridine nucleotides.

Authors:  P S Schein; S Loftus
Journal:  Cancer Res       Date:  1968-08       Impact factor: 12.701

6.  On the relative efficacy of nicotinamide and nicotinic acid as precursors of nicotinamide adenine dinucleotide.

Authors:  B Petrack; P Greengard; H Kalinsky
Journal:  J Biol Chem       Date:  1966-05-25       Impact factor: 5.157

7.  Biliary excretion in foreign compounds. Sulphonamide drugs in the rat.

Authors:  P Millburn; R L Smith; R T Williams
Journal:  Biochem J       Date:  1967-12       Impact factor: 3.857

8.  Biliary excretion of foreign compounds. Biphenyl, stilboestrol and phenolphthalein in the rat: molecular weight, polarity and metabolism as factors in biliary excretion.

Authors:  P Millburn; R L Smith; R T Williams
Journal:  Biochem J       Date:  1967-12       Impact factor: 3.857

9.  The synthesis of [14C] streptozotocin and its distribution and excretion in the rat.

Authors:  E H Karunanayake; D J Hearse; G Mellows
Journal:  Biochem J       Date:  1974-09       Impact factor: 3.857

10.  Gluconeogenesis in the perfused rat liver.

Authors:  R Hems; B D Ross; M N Berry; H A Krebs
Journal:  Biochem J       Date:  1966-11       Impact factor: 3.857

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  17 in total

1.  Effects of streptozotocin on early rat embryos grown in culture.

Authors:  E M Deuchar
Journal:  Experientia       Date:  1978-01-15

2.  Experimental diabetes impairs rat embryo development during the preimplantation period.

Authors:  M Vercheval; R De Hertogh; S Pampfer; I Vanderheyden; B Michiels; P De Bernardi; R De Meyer
Journal:  Diabetologia       Date:  1990-04       Impact factor: 10.122

3.  Pharmacological characterization of the cardiovascular responses elicited by kinin B(1) and B(2) receptor agonists in the spinal cord of streptozotocin-diabetic rats.

Authors:  F Cloutier; R Couture
Journal:  Br J Pharmacol       Date:  2000-05       Impact factor: 8.739

4.  Influence of metabolic control on the blood-retinal barrier in streptozocin diabetic rats.

Authors:  A Kernell; H Dahlkvist; H Arnqvist; J Ludvigsson
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1985       Impact factor: 3.117

5.  Streptozotocin and bone resorption in vitro.

Authors:  R Shires; L V Avioli; S L Teitelbaum
Journal:  Calcif Tissue Int       Date:  1980       Impact factor: 4.333

6.  Effects of streptozotocin-induced long-term diabetes on parietal cell function and morphology in rats.

Authors:  Salim M A Bastaki; Ernest Adeghate; Irwin S Chandranath; Naheed Amir; Saeed Tariq; Rashed S Hameed; Abdu Adem
Journal:  Mol Cell Biochem       Date:  2010-03-17       Impact factor: 3.396

7.  Aldose Reductase Mediates NLRP3 Inflammasome-Initiated Innate Immune Response in Hyperglycemia-Induced Thp1 Monocytes and Male Mice.

Authors:  Pabitra B Pal; Himangshu Sonowal; Kirtikar Shukla; Satish K Srivastava; Kota V Ramana
Journal:  Endocrinology       Date:  2017-10-01       Impact factor: 4.736

8.  The effects of induced type-I diabetes on developmental regulation of insulin & insulin like growth factor-1 (IGF-1) receptors in the cerebellum of rat neonates.

Authors:  Hossein Haghir; Abd-Al-Rahim Rezaee; Mojtaba Sankian; Hamed Kheradmand; Javad Hami
Journal:  Metab Brain Dis       Date:  2013-02-10       Impact factor: 3.584

9.  Constitutive androstane receptor mediates the induction of drug metabolism in mouse models of type 1 diabetes.

Authors:  Bingning Dong; Mohammed Qatanani; David D Moore
Journal:  Hepatology       Date:  2009-08       Impact factor: 17.425

10.  Diabetes in Pregnancy Adversely Affects the Expression of Glycogen Synthase Kinase-3β in the Hippocampus of Rat Neonates.

Authors:  Javad Hami; Razieh Karimi; Hossein Haghir; Mehran Gholamin; Ariane Sadr-Nabavi
Journal:  J Mol Neurosci       Date:  2015-08-05       Impact factor: 3.444

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