Department of Physiology and Anatomy, University of North Texas Health Science Center, Fort Worth, Fort Worth, Texas.
J Neurophysiol. 2020 Aug 1;124(2):591-609. doi: 10.1152/jn.00239.2020. Epub 2020 Jul 22.
Designer receptors exclusively activated by designer drugs (DREADDs) modify cellular activity following administration of the exogenous ligand clozapine--oxide (CNO). However, some reports indicate CNO may have off-target effects. The current studies investigate the use of G DREADDs in CaMKIIa-expressing neurons in the median preoptic nucleus (MnPO). Male Sprague-Dawley rats (250 g) anesthetized with isoflurane were stereotaxically microinjected in the MnPO with the G DREADD (AAV5-CaMKIIa-HM3D-mCherry) or control virus (AAV5-CaMKIIa-mCherry). Following a 2-wk recovery, rats were used for either immunohistochemical Fos analysis or in vitro patch-clamp electrophysiology. In G DREADD-injected rats, CNO induced significant increases in Fos staining in the MnPO and in regions that receive direct or indirect projections from the MnPO. In electrophysiological studies, CNO depolarized and augmented firing frequency in both G DREADD-positive neurons (G DREADD) as well as unlabeled MnPO neurons in slices from G DREADD-injected rats (G DREADDx). G DREADDx neurons also displayed increases in spontaneous postsynaptic current (sPSC) frequency in response to CNO. Additionally, CaMKIIa-positive MnPO neurons, which also express nitric oxide synthase (NOS), were treated with -nitro-l-arginine (l-NNA; competitive inhibitor of NOS) and hemoglobin (NO scavenger) to assess the role of NO in G DREADDx neuron recruitment. Both l-NNA and hemoglobin blocked CNO-induced effects in G DREADDx neurons without affecting G DREADD neurons. These findings indicate that G DREADD-mediated activation of CaMKIIa/NOS expressing neurons in the MnPO can influence the activity of neighboring neurons. Future studies utilizing the use of Gq DREADDs will need to consider the potential recruitment of additional cell populations. Rats were injected in the median preoptic nucleus (MnPO) with either an adeno-associated virus (AAV) and excitatory (G) designer receptor exclusively activated by designer drugs (DREADD) construct or a control AAV. In the G DREADD-injected rats only, clozapine--oxide (CNO) increased Fos staining in the MnPO and its targets and increased neuron action potential frequency. In electrophysiology experiments with slices with DREADD cells, unlabeled cells were activated and this was likely due to nitric oxide release by the DREADD cells.
设计的受体只能被设计的药物激活(DREADD)在给予外源性配体氯氮平-氧化物(CNO)后改变细胞活性。然而,一些报告表明 CNO 可能有脱靶效应。本研究在中脑导水管周围灰质(MnPO)中表达 CaMKIIa 的神经元中使用 G DREADD。用异氟烷麻醉的雄性 Sprague-Dawley 大鼠(250 g)通过立体定向微注射在 MnPO 中注射 G DREADD(AAV5-CaMKIIa-HM3D-mCherry)或对照病毒(AAV5-CaMKIIa-mCherry)。在 2 周的恢复期后,大鼠用于免疫组织化学 Fos 分析或体外膜片钳电生理学研究。在 G DREADD 注射大鼠中,CNO 诱导 MnPO 中 Fos 染色的显著增加,并在直接或间接接受 MnPO 投射的区域中增加。在电生理研究中,CNO 使 G DREADD 阳性神经元(G DREADD)以及来自 G DREADD 注射大鼠切片中的未标记 MnPO 神经元去极化并增加其放电频率(G DREADDx)。G DREADDx 神经元对 CNO 的反应也显示出自发突触后电流(sPSC)频率的增加。此外,用 -硝基-l-精氨酸(NOS 的竞争性抑制剂 l-NNA)和血红蛋白(NO 清除剂)处理表达 CaMKIIa 和一氧化氮合酶(NOS)的中脑导水管周围灰质阳性神经元,以评估 NO 在 G DREADDx 神经元募集中的作用。l-NNA 和血红蛋白均阻止了 CNO 诱导的 G DREADDx 神经元的作用,而不影响 G DREADD 神经元。这些发现表明,在 MnPO 中激活表达 CaMKIIa/NOS 的 G DREADD 可以影响邻近神经元的活性。未来利用 Gq DREADD 的研究需要考虑到可能募集额外的细胞群体。将腺相关病毒(AAV)和兴奋性(G)设计的受体专门激活设计的药物(DREADD)构建体或对照 AAV 注射到大鼠的中脑导水管周围核(MnPO)中。只有在 G DREADD 注射大鼠中,氯氮平-氧化物(CNO)增加了 MnPO 及其靶标中的 Fos 染色,并增加了神经元动作电位频率。在带有 DREADD 细胞的切片的电生理实验中,标记的细胞被激活,这可能是由于 DREADD 细胞释放一氧化氮。