Fedotov V P, Komolov I S, Sadovnikova N V, Maslennikova V G
Probl Endokrinol (Mosk). 1978 Jul-Aug;24(4):57-60.
Partially purified beta cell monolayer cultures were prepared from the pancrease of neonatal Wistar rats by dissociating the cells with a trypsin-collagenase solution. The cultures were grown in medium 199 containing a 10% fetal calf serum and 100 or 300 mg/100 ml glucose. Insulin release from the primary cultures during 12 days was 15 to 20 microunit/culture/day when the cells were grown in the medium containing 300 mg/100 ml glucose. When glucose concentration in the medium was decreased from 300 to 100 mg/ml insulin release fell to 2--5 microunit/culture/day. Theophylline stimulated insulin release in a short-time experiment. Transplantation of a 6--8-day culture in diabetic rats reduced the blood glucose concentration for 1 to 2 days.
通过用胰蛋白酶-胶原酶溶液解离细胞,从新生Wistar大鼠的胰腺中制备部分纯化的β细胞单层培养物。培养物在含有10%胎牛血清和100或300mg/100ml葡萄糖的199培养基中生长。当细胞在含有300mg/100ml葡萄糖的培养基中生长时,原代培养物在12天内的胰岛素释放量为15至20微单位/培养物/天。当培养基中的葡萄糖浓度从300mg/ml降至100mg/ml时,胰岛素释放量降至2 - 5微单位/培养物/天。在短期实验中,茶碱刺激胰岛素释放。将6 - 8天的培养物移植到糖尿病大鼠体内可使血糖浓度降低1至2天。