Laboratory of Brain Information Science in Sports, Center for Education in Liberal Arts and Sciences, Osaka University, Toyonaka, Osaka, Japan.
Laboratory of Brain Information Science in Sports, Graduate School of Frontier Biosciences, Osaka University, Toyonaka, Osaka, Japan.
Psychopharmacology (Berl). 2021 Dec;238(12):3615-3627. doi: 10.1007/s00213-021-05980-y. Epub 2021 Sep 21.
Noradrenaline (NA) is a neuromodulator secreted from noradrenergic neurons in the locus coeruleus to the whole brain depending on the physiological state and behavioral context. It regulates various brain functions including vision via three major adrenergic receptor (AR) subtypes. Previous studies investigating the noradrenergic modulations on vision reported different effects, including improvement and impairment of perceptual visual sensitivity in rodents via β-AR, an AR subtype. Therefore, it remains unknown how NA affects perceptual visual sensitivity via β-AR and what neuronal mechanisms underlie it.
The current study investigated the noradrenergic modulation of perceptual and neuronal visual sensitivity via β-AR in the primary visual cortex (V1).
We performed extracellular multi-point recordings from V1 of rats performing a go/no-go visual detection task under the head-fixed condition. A β-AR blocker, propranolol (10 mM), was topically administered onto the V1 surface, and the drug effect on behavioral and neuronal activities was quantified by comparing pre-and post-drug administration.
The topical administration of propranolol onto the V1 surface significantly improved the task performance. An analysis of the multi-unit activity in V1 showed that propranolol significantly suppressed spontaneous activity and facilitated the visual response of the recording sites in V1. We further calculated the signal-to-noise ratio (SNR), finding that the SNR was significantly improved after propranolol administration.
Pharmacological blockade of β-AR in V1 improves perceptual visual detectability by modifying the SNR of neuronal activity.
去甲肾上腺素(NA)是蓝斑核中的去甲肾上腺素能神经元分泌的神经调质,根据生理状态和行为背景,它会传递到整个大脑。它通过三种主要的肾上腺素能受体(AR)亚型调节各种大脑功能,包括视觉。先前研究发现,去甲肾上腺素能通过β-AR 对视觉产生不同的调制作用,包括改善和损害啮齿动物的知觉视觉敏感性。因此,去甲肾上腺素如何通过β-AR 影响知觉视觉敏感性以及其背后的神经元机制仍不清楚。
本研究旨在研究初级视觉皮层(V1)中通过β-AR 的去甲肾上腺素能调制对知觉和神经元视觉敏感性的影响。
我们在大鼠执行头部固定的视觉检测任务时,从 V1 进行了细胞外多点记录。将β-AR 阻滞剂普萘洛尔(10 mM)局部应用于 V1 表面,并通过比较药物给药前后的行为和神经元活动来量化药物的作用。
将普萘洛尔局部应用于 V1 表面可显著改善任务表现。对 V1 中的多单位活动的分析表明,普萘洛尔显著抑制了自发活动,并促进了 V1 记录部位的视觉反应。我们进一步计算了信噪比(SNR),发现普萘洛尔给药后 SNR 显著提高。
V1 中β-AR 的药理学阻断通过改变神经元活动的 SNR 来改善知觉视觉可检测性。