Sánchez-Martín M M, Cabezas-Delamare M J, Cabezas J A
Departamento de Bioquímica y Biología Molecular, Facultad de Biología, Salamanca, Spain.
Clin Chim Acta. 1996 Nov 29;255(2):173-81. doi: 10.1016/0009-8981(96)06405-4.
The activities of eight lysosomal enzymes were measured by spectrophotometric/spectrofluorimetric techniques in the blood sera of 19-24 apparently healthy women using an oral contraceptive (progestin and oestradiol synthetic derivative, desogestrel+ethinyloestradiol) in comparison with 15-16 non-pregnant women not using contraceptives (controls), in a randomised, double-blind, controlled study. beta-Glucuronidase and arylesterase showed statistically increased activities (P < or = 0.05) in the experimental group in comparison to the controls. No significant differences were found for the remaining enzymes assayed (beta-N-acetylhexosaminidase, alpha-L-fucosidase, alpha-mannosidase, beta-galactosidase, alpha-galactosidase and acid phosphatase). Similar results were obtained when the contraceptive formed by the combination of levonorgestrel and ethinyloestradiol was used by an experimental group of eight healthy women. These results suggest that the significant increases in the above-mentioned activities might be the physiological response of the organism (through catabolic processes catalysed by lysosomal enzymes) to the administration of exogenous synthetic compounds, such as the oral contraceptives used.
在一项随机、双盲、对照研究中,采用分光光度法/荧光分光光度法测定了19至24名明显健康的使用口服避孕药(孕激素和雌二醇合成衍生物,去氧孕烯+炔雌醇)的女性血清中8种溶酶体酶的活性,并与15至16名未使用避孕药的非孕妇女性(对照组)进行了比较。与对照组相比,实验组中的β-葡萄糖醛酸酶和芳基酯酶活性在统计学上显著增加(P≤0.05)。对于所检测的其余酶(β-N-乙酰己糖胺酶、α-L-岩藻糖苷酶、α-甘露糖苷酶、β-半乳糖苷酶、α-半乳糖苷酶和酸性磷酸酶),未发现显著差异。当一组8名健康女性使用左炔诺孕酮和炔雌醇组合的避孕药时,也获得了类似结果。这些结果表明,上述活性的显著增加可能是机体(通过溶酶体酶催化的分解代谢过程)对外源合成化合物(如所用口服避孕药)给药的生理反应。