Harrell L E, Peagler A, Parsons D S
Department of Neurology, Veterans Administration, Birmingham, AL.
Pharmacol Biochem Behav. 1990 Jan;35(1):21-8. doi: 10.1016/0091-3057(90)90198-q.
Previous studies have demonstrated that in male rats hippocampal sympathetic ingrowth (HSI), which is induced by medial septal lesions (MS), is detrimental to recovery of spatial learning. The present study was performed in an attempt to determine if this effect was mediated through adrenergic receptor activity. Adult male Sprague-Dawley rats underwent training on a modified version (i.e., 4 arms baited) of a radial-8-arm maze task. Following attainment of learning criterion animals underwent one of three surgical procedures: CON (sham surgeries); MSGx (MS + superior cervical ganglionectomy--to prevent HSI); MS (MS + sham ganglionectomy). Reacquisition trials were performed in the same manner as initial acquisition except animals were treated with vehicle, propranolol (20 mg/kg), or phentolamine (20 mg/kg) 30 minutes prior to testing. As expected, vehicle-treated MS animals took longer to reacquire the task than MSGx animals, who were in turn more impaired than CON animals. Propranolol (beta-adrenergic antagonist) treatment impaired performance of both the MS and MSGx group, but did not alter the CON group. Phentolamine (alpha-adrenergic antagonist) increased the number of trials to reattain criterion in the CON group, had no effect in the MSGx group, and markedly improved performance in the MS group. The results suggest that HSI mediates its detrimental effects through alpha-receptors, while beta-blockade, in the setting of brain injury, is detrimental to performance regardless of the presence or absence of HSI.
先前的研究表明,在雄性大鼠中,由内侧隔区损伤(MS)诱导的海马交感神经长入(HSI)对空间学习的恢复有害。本研究旨在确定这种效应是否通过肾上腺素能受体活性介导。成年雄性Sprague-Dawley大鼠在改良版(即4个臂有诱饵)的放射状8臂迷宫任务上接受训练。达到学习标准后,动物接受三种手术程序之一:CON(假手术);MSGx(MS + 颈上神经节切除术 - 以防止HSI);MS(MS + 假神经节切除术)。重新获取试验的进行方式与初始获取相同,只是在测试前30分钟给动物注射载体、普萘洛尔(20 mg/kg)或酚妥拉明(20 mg/kg)。正如预期的那样,接受载体治疗的MS动物重新获得任务所需的时间比MSGx动物长,而MSGx动物又比CON动物受损更严重。普萘洛尔(β-肾上腺素能拮抗剂)治疗损害了MS组和MSGx组的表现,但未改变CON组。酚妥拉明(α-肾上腺素能拮抗剂)增加了CON组重新达到标准所需的试验次数,对MSGx组没有影响,并显著改善了MS组的表现。结果表明,HSI通过α受体介导其有害作用,而在脑损伤的情况下,β受体阻滞剂无论是否存在HSI都会对表现产生有害影响。