Department of Basic Biology, Educational and Research Center for Pharmacy, Meiji Pharmaceutical University, Kiyose-shi, Tokyo 204-8588, Japan.
Neuroscience. 2013 Apr 3;235:1-9. doi: 10.1016/j.neuroscience.2013.01.013. Epub 2013 Jan 16.
The roles of the central noradrenergic and serotonergic system in the activity-dependent regulation of ocular dominance plasticity have been a contentious issue. Using c-Fos activity mapping, we have developed a new, straightforward method to measure the strength of ocular dominance plasticity: the number of c-Fos-immunopositive cells in layer IV of rat visual cortex (Oc1B), ipsilateral to the stimulated eye, is a sensitive and reliable measure of the effects of monocular deprivation. Applying this new method, here we studied the unique modification of the degree of c-Fos expression induced in the visual cortex, in that endogenous noradrenaline (NA) and serotonin (5HT) in the cortex were significantly reduced, respectively by specific pharmacological agents. Intraperitoneal injections of N-(2-chloroethyl)-N-ethyl-2-bromobenzylamine (DSP4) and p-chlorophenylalanine (pCPA) selectively impair NA- and 5HT-containing nerve terminals and fibers, respectively. In the visual cortex with strongly reduced NA, the number of c-Fos-immunopositive cells was found remaining significantly decreased in response to stimulation of the deprived eye, while by open eye stimulation the expected increase in c-Fos-immunoreactivity was strongly suppressed, showing values not different from those obtained by monocular stimulation in the normal rats. In contrast, in the visual cortex with strongly reduced 5HT no expected decrease was found in response to stimulation of the deprived eye, while, as is usually the case for the normal animals, a significant increase was still induced in response to open eye stimulation. These findings suggest that the noradrenergic and serotonergic system regulate ocular dominance (OD) plasticity differently: in the NA-depleted cortex the expected increase in c-Fos expression by open eye stimulation was not seen due to strong suppression, whereas in 5HT-depletion, the expected decrease in c-Fos expression was not materialized due to strong suppression. The present findings with c-Fos activity mapping method indicated a novel possibility of the differential regulation of OD plasticity by two types of common monoaminergic systems.
中枢去甲肾上腺素能和 5-羟色胺能系统在眼优势可塑性的活动依赖性调节中的作用一直存在争议。使用 c-Fos 活性映射,我们开发了一种新的、直接的方法来测量眼优势可塑性的强度:刺激眼对侧大鼠视觉皮层(Oc1B)IV 层中 c-Fos 免疫阳性细胞的数量是测量单眼剥夺影响的敏感和可靠指标。应用这种新方法,我们研究了视觉皮层中 c-Fos 表达诱导程度的独特修饰,即皮层中的内源性去甲肾上腺素(NA)和 5-羟色胺(5HT)分别被特定的药理学药物显著降低。腹腔注射 N-(2-氯乙基)-N-乙基-2-溴苯甲胺(DSP4)和对氯苯丙氨酸(pCPA)分别选择性地损害 NA 和 5HT 含量的神经末梢和纤维。在 NA 含量明显降低的视皮层中,发现 c-Fos 免疫阳性细胞的数量在对剥夺眼的刺激下仍显著减少,而在睁眼刺激下,c-Fos 免疫反应性的预期增加受到强烈抑制,其值与正常大鼠的单眼刺激获得的值没有差异。相比之下,在 5HT 含量明显降低的视皮层中,对剥夺眼的刺激没有发现预期的减少,而与通常的正常动物情况一样,对睁眼刺激仍诱导显著增加。这些发现表明,去甲肾上腺素能和 5-羟色胺能系统对眼优势(OD)可塑性的调节方式不同:在去甲肾上腺素耗尽的皮层中,由于强烈抑制,预期的睁眼刺激下 c-Fos 表达的增加没有出现,而在 5HT 耗竭中,由于强烈抑制,预期的 c-Fos 表达减少没有实现。本研究采用 c-Fos 活性映射方法,为两种常见单胺能系统对 OD 可塑性的差异调节提供了新的可能性。