Lopez-Sela P, Brime J, Díaz F, Marín B, Costales M, Vijande M
Departamento de Biología Funcional, Universidad de Oviedo, Spain.
Eur J Pharmacol. 1991 Jul 23;200(1):125-9. doi: 10.1016/0014-2999(91)90674-f.
Insulin-induced drinking (IID) in male Wistar rats, evoked by administering 5 U/kg of crystalline porcine insulin i.p., was significantly decreased by propranolol (0.1 and 0.5 mg/kg s.c.) after 1 and 2 h. The blood glucose of rats treated with a much higher dose of propranolol (10 mg/kg body weight) and insulin did not differ from that of rats treated solely with insulin after 30 and 120 min. Atenolol (0.5 mg/kg s.c.) caused a reduction in IID after 1 and 2h. Butoxamine (1 mg/kg s.c.) also reduced IID after 1 and 2h, and at 0.5 mg/kg after 1h. The alpha-blocker, phenoxybenzamine (10 mg/kg s.c.), had the opposite effect, stimulating IID after 2h. There is no direct evidence that insulin activated the sympathetic system at the doses used in these experiments. Nevertheless, the results reported here seem to be compatible with the involvement of the sympathetic system in IID, possible through the renin-angiotensin system.
给雄性Wistar大鼠腹腔注射5 U/kg结晶猪胰岛素所诱发的胰岛素诱导饮水(IID),在1小时和2小时后,经皮下注射普萘洛尔(0.1和0.5 mg/kg)可使其显著降低。在30分钟和120分钟后,用更高剂量普萘洛尔(10 mg/kg体重)和胰岛素处理的大鼠的血糖与仅用胰岛素处理的大鼠无异。阿替洛尔(0.5 mg/kg皮下注射)在1小时和2小时后使IID降低。布托沙明(1 mg/kg皮下注射)在1小时和2小时后也降低了IID,在1小时后0.5 mg/kg剂量时也有此效果。α受体阻滞剂酚苄明(10 mg/kg皮下注射)则有相反作用,在2小时后刺激IID。没有直接证据表明在这些实验中所用剂量的胰岛素激活了交感神经系统。然而,此处报道的结果似乎与交感神经系统参与IID相符,可能是通过肾素 - 血管紧张素系统。