Nauman J, Dung N T, Porta S, Sadjak A
Horm Metab Res. 1984 Oct;16(10):521-4. doi: 10.1055/s-2007-1014839.
Especially coated adrenaline tablets (A) or placebo tablets (P) which release linearly the hormone were implanted in male Wistar rats. Six hours later animals were sacrificed and kinetic parameters of T3-125I binding to nuclear receptor, intracellular distribution of endogenous T3 and activities of alfa-GPD and ME were investigated. The association constant values (Ka) of nuclear receptor were increased after pretreatment with 7.5, 15 and 45 mg A tablets and were 1.07, 1.35 and 1.48 X 10(9) M-1 vs 0.85 X 10(8) M-1 value seen after P. The maximal binding capacity (MBC) values decreased after pretreatment with the same doses of A and were 0.044, 0.036 and 0.025 pmol T3/100 micrograms DNA vs. 0.065 pmol T3/100 micrograms DNA in P pretreated. Adrenaline pretreatment significantly increased the amount of endogenous T3 present in liver nuclei while the amount of T3 present in cytosol decreased. Activity of mitochondrial alfa-GPD was increased after 15 and 45 mg of A. Significant rise of activity of cytosol ME was seen only after pretreatment with 45 mg of A.
将特别包衣的能线性释放激素的肾上腺素片(A)或安慰剂片(P)植入雄性Wistar大鼠体内。6小时后处死动物,研究T3-125I与核受体结合的动力学参数、内源性T3的细胞内分布以及α-GPD和ME的活性。用7.5、15和45毫克A片预处理后,核受体的缔合常数(Ka)值增加,分别为1.07、1.35和1.48×10⁹ M⁻¹,而P预处理后的值为0.85×10⁸ M⁻¹。用相同剂量的A预处理后,最大结合容量(MBC)值降低,分别为0.044、0.036和0.025皮摩尔T3/100微克DNA,而P预处理后的为0.065皮摩尔T3/100微克DNA。肾上腺素预处理显著增加了肝细胞核中内源性T3的含量,而细胞质中T3的含量减少。15和45毫克A处理后,线粒体α-GPD的活性增加。仅在45毫克A预处理后,细胞质ME的活性才显著升高。