Russell J E, Gennari C, Imbimbo B, Avioli L V
Horm Metab Res. 1985 Aug;17(8):402-5. doi: 10.1055/s-2007-1013558.
Male Sprague-Dawley rats were injected with 1 mg/100 g bw/day of prednisone, 1.25 mg/1--g bw/day of deflazacort, or its metabolite, for a period of 20 days. Epiphyseal cartilage slices were incubated in a modified Krebs Ringer bicarbonate buffer, at 37 degrees C for 60 min, with either 14C-1- or 14C-6-glucose to quantitate both the absolute and relative rates of pentose shunt versus aerobic and anaerobic glycolytic activity, respectively. Measurements of both total and radioactive glucose uptake, lactate production and 14CO2 generation were expressed as either mumoles or DPM/mg cellular DNA/hr, respectively. This study demonstrated: (1) chronic prednisone administration decreased anaerobic glycolysis (glucose uptake and lactate production) 3-fold (P less than 0.01); (2) prednisone on a chronic basis produced no measured alteration in either the pentose shunt or Kreb's cycle activity; (3) both deflazacort and the deflazacort metabolite significantly stimulated (P less than 0.02) anaerobic glycolytic activity in epiphyseal cartilage tissue. In contrast to prednisone, the administration of either deflazacort or its L-6485 metabolite did not inhibit the glycolytic pathway of metabolism so necessary for epiphyseal cartilage growth and mineralization.
将雄性斯普拉格-道利大鼠每天按1毫克/100克体重的剂量注射泼尼松、按1.25毫克/100克体重的剂量注射地夫可特或其代谢产物,持续20天。将骨骺软骨切片在改良的krebs林格碳酸氢盐缓冲液中于37℃孵育60分钟,分别加入14C-1-葡萄糖或14C-6-葡萄糖,以定量磷酸戊糖途径相对于有氧和无氧糖酵解活性的绝对和相对速率。总葡萄糖摄取量、放射性葡萄糖摄取量、乳酸生成量和14CO2生成量的测量结果分别以微摩尔或每毫克细胞DNA/小时的每分钟衰变数表示。本研究表明:(1)长期给予泼尼松可使无氧糖酵解(葡萄糖摄取和乳酸生成)降低3倍(P<0.01);(2)长期给予泼尼松对磷酸戊糖途径或三羧酸循环活性未产生可测量的改变;(3)地夫可特及其代谢产物均显著刺激(P<0.02)骨骺软骨组织中的无氧糖酵解活性。与泼尼松不同,给予地夫可特或其L-6485代谢产物均未抑制对骨骺软骨生长和矿化至关重要的糖酵解代谢途径。