Godfrey Donald A, Park Jami L, Dunn Jon D, Ross C David
Department of Neurology and Division of Otolaryngology & Dentistry, Department of Surgery, University of Toledo College of Medicine and Life Sciences, Toledo, Ohio.
Department of Neurology and Division of Otolaryngology & Dentistry, Department of Surgery, University of Toledo College of Medicine and Life Sciences, Okmulgee, Oklahoma.
HSOA J Otolaryngol Head Neck Surg. 2020;6(2). doi: 10.24966/ohns-010x/100045. Epub 2020 Jul 22.
Kainic acid injections have been used to destroy neuron somata in particular regions without damaging fiber tracts. We injected a solution of kainic acid into the region of the rat superior olivary complex in an effort to destroy its cholinergic projections to the cochlea and cochlear nucleus, which derive especially from the lateral superior olivary nucleus and ventral nucleus of the trapezoid body. In the lateral superior olivary nucleus, there were relatively small but fairly consistent decreases of choline acetyltransferase (ChAT) activity, larger decreases of acetylcholinesterase (AChE) activity, and consistent decreases of malate dehydrogenase activity, as a marker for oxidative metabolism. Other superior olivary regions were less affected by the kainic acid injections, but most showed overall significant decreases of AChE activity. Our results suggest that the cholinergic neurons giving rise to the centrifugal pathways to the cochlea and cochlear nucleus are more resistant to the effects of kainic acid than are those that receive major ascending input from the cochlear nucleus and project to higher levels of the auditory system. Comparison with published anatomical studies suggests that this resistance to the effects of kainic acid is related to relatively little glutamatergic input to the somata and proximal dendrites of these neurons. We also found a consistent approximately 16 % decrease of ChAT activity in the injected-side facial nerve root, which is most easily explained as a small effect of kainic acid on the facial nerve fibers passing through the injection site.
海人酸注射已被用于破坏特定区域的神经元胞体,而不损伤纤维束。我们将海人酸溶液注射到大鼠上橄榄复合体区域,试图破坏其向耳蜗和耳蜗核的胆碱能投射,这些投射尤其来自外侧上橄榄核和斜方体腹侧核。在外侧上橄榄核中,胆碱乙酰转移酶(ChAT)活性有相对较小但相当一致的下降,乙酰胆碱酯酶(AChE)活性有较大下降,而苹果酸脱氢酶活性作为氧化代谢的标志物有一致下降。其他上橄榄区域受海人酸注射的影响较小,但大多数总体上显示出AChE活性的显著下降。我们的结果表明,产生至耳蜗和耳蜗核的离心通路的胆碱能神经元比那些从耳蜗核接受主要上行输入并投射到听觉系统更高水平的神经元对海人酸的影响更具抵抗力。与已发表的解剖学研究比较表明,这种对海人酸影响的抵抗力与这些神经元的胞体和近端树突相对较少的谷氨酸能输入有关。我们还发现注射侧面神经根部的ChAT活性持续下降约16%,这最容易解释为海人酸对穿过注射部位的面神经纤维有轻微影响。