Bagi Eva Eszter, Fekete Eva, Lénárd László
Institute of Physiology and Neurophysiology Research Group of the Hungarian Academy of Sciences, Pécs University Medical School, Szigeti Street 12, H-7624 Pécs, Hungary.
Brain Res. 2003 Jul 11;977(2):199-208. doi: 10.1016/s0006-8993(03)02680-5.
Different doses of angiotensin II (AII) or angiotensin III (AIII) microinjections into the zona incerta have been studied on drinking of rats in separate experiments during the consequent 60-min-daily-drinking period. Also, the dipsogen power of only the effective dose of AII and AIII was compared to vehicle treated rats. After, angiotensin receptor (AT(1), AT(2)) antagonists on AII or AIII induced drinking were tested. In the first and second experiments only the 100 ng AII and the 200 ng AIII increased water intake significantly. In the third experiment the AII started its dipsogen effect earlier, at the 5 min measuring time, compared to the AIII. Both effects kept on lasting parallel from the 10 min on. Considering the antagonist pre-treatments in the fourth experiment, animals were injected with 90 ng losartan, an AT(1) antagonist, 180 ng PD 123319 or 200 ng CGP 42112, both AT(2) antagonists, respectively. Both AII and AIII increased water consumption. The effect of AII could be blocked by losartan, but not by PD 123319 or CGP 42112. On the other hand, the effect of AIII could not be blocked by losartan, but by both the PD 123319 and CGP 42112. Since, the effects of AII, AIII and angiotensin antagonists have not been tested in the zona incerta, the finding that water intake increased after AII or AIII injections and it could be blocked only by either of the antagonists suggests that AT(1) and AT(2) receptors play partially different roles in the regulation of water intake.
在随后每天60分钟的饮水期内,通过单独实验研究了向大鼠未定带内微量注射不同剂量的血管紧张素II(AII)或血管紧张素III(AIII)对其饮水的影响。此外,还将仅有效剂量的AII和AIII的致渴能力与接受溶剂处理的大鼠进行了比较。之后,测试了血管紧张素受体(AT(1)、AT(2))拮抗剂对AII或AIII诱导饮水的影响。在第一个和第二个实验中,仅100 ng的AII和200 ng的AIII显著增加了水摄入量。在第三个实验中,与AIII相比,AII在5分钟测量时间时更早开始其致渴作用。从10分钟起,两种作用持续平行。考虑到第四个实验中的拮抗剂预处理,分别给动物注射了90 ng的氯沙坦(一种AT(1)拮抗剂)、180 ng的PD 123319或200 ng的CGP 42112(均为AT(2)拮抗剂)。AII和AIII均增加了水消耗。AII的作用可被氯沙坦阻断,但不能被PD 123319或CGP 42112阻断。另一方面,AIII的作用不能被氯沙坦阻断,但可被PD 123319和CGP 42112两者阻断。由于尚未在未定带中测试AII、AIII和血管紧张素拮抗剂的作用,AII或AIII注射后水摄入量增加且仅可被其中一种拮抗剂阻断这一发现表明,AT(1)和AT(2)受体在水摄入调节中发挥部分不同的作用。