CORTISOL PRODUCTION-RATE IN CHILDREN BY GAS-CHROMATOGRAPHY MASS-SPECTROMETRY USING [1,2,3,4-C-13]CORTISOL

被引:15
作者
KRAAN, GPB
DRAYER, NM
机构
[1] Division of Endocrinology, Department of Pediatrics, University of Groningen, Groningen
关键词
children; CPR; gas chromatography/mass spectrometry; steroids; [!sup]13[!/sup]C[!sub]4[!/sub]]cortisol;
D O I
10.1016/0039-128X(90)90104-J
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A urinary method of determining the cortisol production rate (CPR) in children was studied under physiologic conditions by administration of low amounts of [1,2,3,4-13C]cortisol. The CPR in three patients with multiple pituitary deficiency ranged from 7 to 16 nmoles d-1 m-2, and the CPR in three patients with congenital adrenal hyperplasia (CAH) due to 11β-hydroxylase deficiency (11βOHD) and 17α-hydroxylase deficiency (17αOHD) from 0.1 to 2.11 μmmoles d-1 m-2. Results showed that with this method, very low CPRs can be reliably measured. The metabolism of [13C4] cortisol or [9,12,12-2H]cortisol was compared with that of native cortisol in adrenalectomized piglets. For the urinary cortisol metabolites, small to substantial differences in isotope dilution were noted relative to that in the original cortisol mixture. With [13C4]cortisol, the so-called secondary isotope effects were approximately 2% to 3% for tetrahydrocortisone (THE) and tetrahydrocortisol (THF), and about 10% for the cortolones, relative to the cortisol mixture. When [2H3] cortisol was used, the cortisol metabolites THE and THF contained only two deuterium atoms. Together with this apparent loss of one deuterium atom, the secondary isotope effects in these steroids amounted to 5% to 10%. It was concluded that [13C4] cortisol was the better tracer to use for the measurement of urinary CPR. © 1992.
引用
收藏
页码:159 / 164
页数:6
相关论文
共 20 条
[1]  
Clayton, Assessment of pituitary-adrenal function in children, Memoirs of the Society for Endocrinology, no. 17. The Investigation of Hypothalamic-Pitutary-Adrenal Function, pp. 237-246, (1968)
[2]  
Kraan, Chapman, Drayer, Nagel, Wolthers, Colenbrander, Fentener-van Vlissingen, Metabolic dissimilarity between [9,12,12-<sup>2</sup>H]cortisol and natural Cortisol in vivo. Can deuterated cortisol be used for the measurement of the urinary cortisol production rate?, Biomed Environ Mass Spectrum, 18, pp. 662-667, (1989)
[3]  
Zomer, Wijnherg, Drayer, The synthesis of [1,2,3,4-<sup>13</sup>C]cortisol, Steroids, 44, pp. 293-300, (1984)
[4]  
Gehan, George, Estimation of body surface area from height and weight, Cancer Chemother Rep, 54, pp. 225-235, (1979)
[5]  
Chapman, Kraan, Drayer, Nagel, Wolthers, Determination of the urinary cortisol production rate using [1,2,3,4,-<sup>13</sup>C]cortisol. Isotope dilution analyses at very small enrichments, Biomed Environ Mass Spectrom, 14, pp. 73-82, (1987)
[6]  
Winter, Cerone-McLernon, O'Rourke, Ponticorvo, Bokkenheuser, Formation of 20β-dihydrosteroids by anaerobic bacteria, J Steroid Biochem, 17, pp. 661-667, (1982)
[7]  
Kraan, Chapman, Drayer, Colenbrander, Buwalda, Kinetic measurement of the urinary production rate of cortisol in male piglets: is the prerequisite ‘collection until all label has disappeared’ necessary?, J Endocrinol, 111, pp. 439-448, (1986)
[8]  
Chapman, Kraan, Drayer, Nagel, Wolthers, Colenhrander, Fentener-van Vlissingen, Are [<sup>13</sup>C]cortisol and [<sup>3</sup>C]cortisol metabolized identically to natural cortisol in adrenalectomized piglets?, Biomed Environ Mass Spectrom, 17, pp. 343-353, (1988)
[9]  
Bush, Chromatography of Steroids, pp. 363-365, (1961)
[10]  
Kenny, Preeyasombal, Migeon, Cortisol production rate. 11. Normal infants, children and adults, Pediatrics, 37, pp. 34-42, (1966)