Abdi, A., Mallet, N., Mohamed, F. Y., Sharott, A., Dodson, P. D., Nakamura,K. C., et al. (2015). Prototypic and arkypallidal neurons in the dopamine-intact external globus pallidus. J. Neurosci. 35, 6667–6688. doi: 10.1523/JNEUROSCI. 4662-14.2015
Abe, T., Kiyonari, H., Shioi, G., Inoue, K., Nakao, K., Aizawa, S., et al. (2011). Establishment of conditional reporter mouse lines at ROSA26 locus for live cell imaging. Genesis 49, 579–590. doi: 10.1002/dvg.20753
Ábrahám, I. M., and Kovács, K. J. (2000). Postnatal handling alters the activation of stress-related neuronal circuitries. Eur. J. Neurosci. 12, 3003–3014. doi: 10.1046/ j.1460-9568.2000.00176.x
Aizawa, H., Bianco, I. H., Hamaoka, T., Miyashita, T., Uemura, O., Concha,M. L., et al. (2005). Laterotopic representation of left-right information onto the dorso-ventral axis of a zebrafish midbrain target nucleus. Curr. Biol. 15, 238–243. doi: 10.1016/j.cub.2005.01.014
Amo, R., Aizawa, H., Takahoko, M., Kobayashi, M., Takahashi, R., Aoki, T., et al. (2010). Identification of the zebrafish ventral habenula as a homolog of the mammalian lateral habenula. J. Neurosci. 30, 1566–1574. doi: 10.1523/ JNEUROSCI.3690-09.2010
Anastasiades, P. G., and Butt, S. J. B. (2011). Decoding the transcriptional basis for GABAergic interneuron diversity in the mouse neocortex. Eur. J. Neurosci. 34, 1542–1552. doi: 10.1111/j.1460-9568.2011.07904.x
Armario, A., and Nadal, R. (2013). Individual differences and the characterization of animal models of psychopathology: a strong challenge and a good opportunity. Front. Pharmacol. 4:137. doi: 10.3389/fphar.2013.00137
Béracochéa, D., Tronche, C., Coutan, M., Dorey, R., Chauveau, F., and Piérard,C. (2011). Interaction between diazepam and hippocampal corticosterone after acute stress: impact on memory in middle-aged mice. Front. Behav. Neurosci. 5:14. doi: 10.3389/fnbeh.2011.00014
Bubser, M., and Deutch, A. (1999). Stress induces Fos expression in neurons of the thalamic paraventricular nucleus that innervate limbic forebrain sites. Synapse 32, 13–22. doi: 10.1002/(SICI)1098-2396(199904)32:1<13::AID-SYN2>3.0. CO;2-R
Chou, M. Y., Amo, R., Kinoshita, M., Cherng, B. W., Shimazaki, H., Agetsuma, M., et al. (2016). Social conflict resolution regulated by two dorsal habenular subregions in zebrafish. Science 352, 87–90. doi: 10.1126/science.aac9508
Concha, M. L., Russell, C., Regan, J. C., Tawk, M., Sidi, S., Gilmour, D. T., et al. (2003). Local tissue interactions across the dorsal midline of the forebrain establish CNS laterality. Neuron 39, 423–438. doi: 10.1016/S0896-6273(03)00437-9
Concha, M. L., and Wilson, S. W. (2001). Asymmetry in the epithalamus of vertebrates. J. Anat. 199, 63–84. doi: 10.1046/j.1469-7580.2001.19910063.x
Conner, J. M., Culberson, A., Packowski, C., Chiba, A. A., and Tuszynski, M. H. (2003). Lesions of the basal forebrain cholinergic system impair task acquisition and abolish cortical plasticity associated with motor skill learning. Neuron 38, 819–829. doi: 10.1016/S0896-6273(03)00288-5
Cullinan, W. E., Herman, J. P., Battaglia, D. E., Akil, H., and Watson, S. J. (1995). Pattern and time course of immediate early gene expression in rat brain following acute stress. Neuroscience 64, 477–505. doi: 10.1016/0306-4522(94)00355-9
de Olmos, J. S., and Heimer, L. (1999). The concepts of the ventral striatopallidal system and extended amygdala. Ann. N.Y. Acad. Sci. 877, 1–32. doi: 10.1111/j. 1749-6632.1999.tb09258.x
Dodson, P. D., Larvin, J. T., Duffell, J. M., Garas, F. N., Doig, N. M., Kessaris, N., et al. (2015). Distinct developmental origins manifest in the specialized encoding of movement by adult neurons of the external globus pallidus. Neuron 86, 501–513. doi: 10.1016/j.neuron.2015.03.007
Duque, A., Balatoni, B., Detari, L., and Zaborszky, L. (2000). EEG correlation of the discharge properties of identified neurons in the basal forebrain.J. Neurophysiol. 84, 1627–1635. doi: 10.1152/jn.2000.84.3.1627
Evans, C. S., Evans, L., and Marler, P. (1993). On the meaning of alarm calls: functional references in an avian vocal system. Anim. Behav. 46, 23–28. doi: 10.1006/anbe.1993.1158
Flames, N., Pla, R., Gelman, D. M., Rubenstein, J. L. R., Puelles, L., and Marín,O. (2007). Delineation of multiple subpallial progenitor domains by the combinatorial expression of transcriptional codes. J. Neurosci. 27, 9682–9695. doi: 10.1523/JNEUROSCI.2750-07.2007
Gaier, E. D., Rodriguiz, R. M., Ma, X. M., Sivaramakrishnan, S., Bousquet- Moore, D., Wetsel, W. C., et al. (2010). Haploinsufficiency in peptidylglycine alpha-amidating monooxygenase leads to altered synaptic transmission in the amygdala and impaired emotional responses. J. Neurosci. 30, 13656–13669. doi: 10.1523/JNEUROSCI.2200-10.2010
Gallo, F. T., Katche, C., Morici, J. F., Medina, J. H., and Weisstaub, N. V. (2018). Immediate early genes, memory and psychiatric disorders: focus on c-Fos, Egr1 and Arc. Front. Behav. Neurosci. 12:79. doi: 10.3389/fnbeh.2018.00079
Gastard, M., Jensen, S. L., Martin, J. R. III, Williams, E. A., and Zahm, D. S. (2002). The caudal sublenticular region/anterior amygdaloid area is the only part of the rat forebrain and mesopontine tegmentum occupied by magnocellular cholinergic neurons that receives outputs from the central division of extended amygdala. Brain Res. 957, 207–222. doi: 10.1016/s0006-8993(02)03513-8
Goard, M., and Dan, Y. (2009). Basal forebrain activation enhances cortical coding of natural scenes. Nat. Neurosci. 12, 1444–1451. doi: 10.1038/nn.2402
Granger, A., Mulder, N., Saunders, A., and Sabatini, B. (2016). Cotransmission of acetylcholine and GABA. Neuropharmacology 100, 40–46. doi: 10.1016/j. neuropharm.2015.07.031
Gritti, I., Henny, P., Galloni, F., Mainville, L., Mariotti, M., and Jones, B. E. (2006). Stereological estimates of the basal forebrain cell population in the rat, including neurons containing choline acetyltransferase, glutamic acid decarboxylase or phosphate-activated glutaminase and colocalizing vesicular glutamate transporters. J. Neurosci. 143, 1051–1064. doi: 10.1016/j.neuroscience.2006. 09.024
Gritti, I., Manns, I. D., Mainville, L., and Jones, B. E. (2003). Parvalbumin, calbindin, or calretinin in cortically projecting and GABAergic, cholinergic, or glutamatergic basal forebrain neurons of the rat. J. Comp. Neurol. 458, 11–31. doi: 10.1002/cne.10505
Guzowski, J. F., McNaughton, B. L., Barnes, C. A., and Worley, P. F. (1999). Environment-specific expression of the immediate-early gene Arc in hippocampal neuronal ensembles. Nat. Neurosci. 2, 1120–1124. doi: 10.1038/ 16046
Guzowski, J. F., Setlow, B., Wagner, E. K., and McGaugh, J. L. (2001). Experience- dependent gene expression in the rat hippocampus after spatial learning: a comparison of the immediate-early genes Arc, c-fos, and zif268. J. Neurosci. 21, 5089–5098. doi: 10.1523/JNEUROSCI.21-14-05089.2001
Guzowski, J. F., Timlin, J. A., Roysam, B., McNaughton, B. L., Worley, P. F., and Barnes, C. A. (2005). Mapping behaviorally relevant neural circuits with immediate-early gene expression. Curr. Opin. Neurobiol. 15, 599–606. doi: 10. 1016/j.conb.2005.08.018
Heimer, L., Van Hoesen, G. W., Trimble, M., and Zahm, D. S. (2008). “The anatomy of the basal forebrain,” in Anatomy of Neuropsychiatry: The New Anatomy of The Basal Forebrain and Its Implications for Neuropsychiatric Illness (Amsterdam: Elsevier), 27–67.
Hernández, V. M., Hegeman, D. J., Cui, Q., Kelver, D. A., Fiske, M. P., Glajch, K. E., et al. (2015). Palvalbumin+ neurons and Npas1+ neurons are distinct neuron classes in the mouse external globus pallidus. J. Neurosci. 35, 11830–11847. doi: 10.1523/JNEUROSCI.4672-14.2015
Hontanilla, B., Parent, A., de las Heras, S., and Gimenez-Amaya, J. M. (1998). Distribution of calbindin D-28k and parvalbumin neurons and fibers in the rat basal ganglia. Brain. Res. Bull. 47, 107–116. doi: 10.1016/S0361-9230(98)00 035-5
Ichijo, H., Nakamura, T., Kawaguchi, M., and Takeuchi, Y. (2017). An evolutionary hypothesis of binary opposition in functional incompatibility about habenular asymmetry in vertebrates. Front. Neurosci. 10:595. doi: 10.3389/fnins.2016. 00595
Ishida, Y., Hashiguchi, H., Ishizuka, Y., Todaka, K., Kuwahara, I., Mitsuyama, Y., et al. (2000). Basal expression of c-Fos and Zif268 in the rat basal ganglia: immunohistochemical characterization of striatal Zif268-positive neruons. Eur.
J. Neurosci. 12, 771–775. doi: 10.1046/j.1460-9568.2000.00968.x
Jones, B. E. (2008). Modulation of cortical activation and behavioral arousal by cholinergic and orexinergic systems. Ann. N.Y. Acad. Sci. 1129, 26–34. doi: 10.1196/annals.1417.026
Karolewicz, B., and Paul, I. A. (2001). Group housing of mice increases immobility and antidepressant sensitivity in the forced swim and tail suspension tests. Eur.J. Pharmacol. 415, 197–201. doi: 10.1016/s0014-2999(01)00830-5
Kemppainen, S., and Pitkänen, A. (2000). Distribution of parvalbumin, calretinin, and calbindin-D28k immunoreactivity in the rat amygdaloid complex and colocalization with γ-aminobutyric acid. J. Comp. Neurol. 426, 441–467. doi: 10.1002/1096-9861(20001023)426:3<441::aid-cne8>3.0.co;2-7
Kovács, L. Á, Schiessl, J. A., Nafz, A. E., Csernus, V., and Gaszner, B. (2018). Both basal and acute restraint stress-induced c-Fos expression is influenced by age in the extended amygdala and brainstem stress centers in male rats. Front. Aging Neurosci. 10:248. doi: 10.3389/fnagi.2018.00248
Lin, D., Boyle, M. P., Dollar, P., Lee, H., Lein, E. S., Perona, P., et al. (2011). Functional identification of an aggression locus in the mouse hypothalamus. Nature 470, 221–226. doi: 10.1038/nature09736
Lomnicki, A. (1978). Individual differences between animals and the natural regulation of their numbers. J. Anim. Ecol. 47, 461–475. doi: 10.2307/3794
Mallet, N., Michlem, B. R., Henny, P., Brown, M. T., Williams, C., Bolam, J. P., et al. (2012). Dichotomous organization of the external globus pallidus. Neuron 74, 1075–1086. doi: 10.1016/j.neuron.2012.04.027
Marín, O., and Rubenstein, J. L. R. (2001). A long, remarkable journey: tangential migration in the telencephalon. Nat. Rev. Neurosci. 2, 780–790. doi: 10.1038/ 35097509
Masuda, R., Fukuda, M., Ono, T., and Endo, S. (1997). Neuronal responses at the sight of objects in monkey basal forebrain subregions during operant isual tasks. Neurobiol. Learn. Mem. 67, 181–196. doi: 10.1006/nlme.1996.3756
Mesulam, M. M., Mufson, E. J., Levey, A. I., and Wainer, B. H. (1983). Cholinergic innervation of cortex by the basal forebrain: cytochemistry and cortical connections of the septa1 area, diagonal band nuclei, nucleus basalis (substantia innominata), and hypothalamus in the rhesus monkey. J. Comp. Neurol. 214, 170–197. doi: 10.1002/cne.902140206
Numa, C., Nagai, H., Taniguchi, M., Nagai, M., Shinohara, R., and Furuyashiki,T. (2019). Social defeat stress-specific increase in c-Fos expression in the extended amygdala in mice: involvement of dopamine D1 receptor in the medial prefrontal cortex. Sci. Rep. 9:16670. doi: 10.1038/s41598-019-52997-7
Ohkawa, N., Saitoh, Y., Suzuki, A., Tsujimura, S., Murayama, E., Kosugi, S., et al. (2015). Artificial association of pre-stored information to generate a qualitatively new memory. Cell. Rep. 11, 261–269. doi: 10.1016/j.celrep.2015. 03.017
Ono, M., Yanagawa, Y., and Koyano, K. (2005). GABAergic neurons in inferior colliculus of the GAD67-GFP knock-in mouse: electrophysiological and morphological properties. J. Neurosci. Res. 51, 475–492. doi: 10.1016/j.neures. 2004.12.019
Otake, K., Kin, K., and Nakamura, Y. (2002). Fos expression in afferents to the rat midline thalamus following immobilization stress. J. Neurosci. Res. 43, 269–282. doi: 10.1016/S0168-0102(02)00042-1
Parikh, V., and Sarter, M. (2008). Cholinergic mediation of attention. Contributions of phasic and tonic increases in prefrontal cholinergic activity. Ann. N.Y. Acad. Sci. 1129, 225–235. doi: 10.1196/annals.1417.021
Paxinos, G., and Franklin, K. B. J. (2013). The Mouse Brain in Stereotaxic Coordinates, 4th Edn. San Diego, CA: Academic Press.
Rice, K., Viscomi, B., Riggins, T., and Redcay, E. (2014). Amygdala volume linked to individual differences in mental state inference in early childhood and adulthood. Dev. Cogn. Neurosci. 8, 153–163. doi: 10.1016/j.dcn.2013.09.003
Riedel, A., Härtig, W., Seeger, G., Gärtner, U., Brauer, K., and Arendt, T. (2002). Principles of rat subcortical forebrain organization: a study using histological techniques and multiple fluorescence labeling. J. Chem. Neuroanat. 23, 75–104. doi: 10.1016/S0891-0618(01)00142-9
Rogers, L. J. (2000). Evolution of hemispheric specialization: advantages and disadvantages. Brain Lang. 73, 236–253. doi: 10.1006/brln.2000.2305
Rogers, L. J., and Anson, J. M. (1979). Lateralization of function in the chicken fore- brain. Pharmacol. Biochem. Behav. 10, 679–686. doi: 10.1016/0091-3057(79)90320-4
Schaefer, A., Braver, T. S., Reynolds, J. R., Burgess, G. C., Yarkoni, T., and Gray, J. R. (2006). Individual differences in amygdala activity predict response speed during working memory. J. Neurosci. 26, 10120–10128. doi: 10.1523/ JNEUROSCI.2567-06.2006
Senba, E., and Ueyama, T. (1997). Stress-induced expression of immediate early genes in the brain and peripheral organs of the rat. Neurosci. Res. 29, 183–207. doi: 10.1016/S0168-0102(97)00095-3
Stamps, J. A., Briffa, M., and Biro, P. A. (2012). Unpredictable animals: individual differences in intraindividual variability (IIV). Anim. Behav. 83, 1325–1334. doi: 10.1016/j.anbehav.2012.02.017
Sugimoto, Y., Yamada, J., and Noma, T. (1998). Effects of anxiolytics, diazepam and tandospirone, on immobilization stress-induced hyperglycemia in mice. Life Sci. 63, 1221–1226. doi: 10.1016/s0024-3205(98)00384-1
Sztainberg, Y., Kuperman, Y., Justice, N., and Chen, A. (2011). An anxiolytic role for CRF receptor type 1 in the globus pallidus. J. Neurosci. 31, 17416–17424. doi: 10.1523/JNEUROSCI.3087-11.2011
Tamamaki, N., Yanagawa, Y., Tomioka, R., Miyazaki, J., Obata, K., and Kaneko, T. (2003). Green fluorescent protein expression and colocalization with calretinin, parvalbumin, and somatostatin in the GAD67-GFP knock-in mouse. J. Comp. Neurol. 467, 60–79. doi: 10.1002/cne.10905
Tanaka, D. H., Li, S., Mukae, S., and Tanabe, T. (2019). Genetic access to gustatory disgust-associated neurons in the interstitial nucleus of the posterior limb of the anterior commissure in male mice. Neuroscience 413, 45–63. doi: 10.1016/j. neuroscience.2019.06.021
Taniguchi, H., He, M., Wu, P., Kim, S., Paik, R., Sugino, K., et al. (2011). A resource of Cre driver lines for genetic targeting of GABAergic neurons in cerebral cortex. Neuron 71, 995–1013. doi: 10.1016/j.neuron.2011.07.026
Umemoto, S., Kawai, Y., Ueyama, T., and Senba, E. (1997). Chronic glucocorticoid administration as well as repeated stress affects the subsequent acute immobilization stress-induced expression of immediate early genes but not that of NGFI-A. J. Neurosci. 80, 763–773. doi: 10.1016/S0306-4522(97)0 0050-X Yang, R. J., Mozhui, K., Karlsson, R. M., Cameron, H. A., Williams,R. W., and Holmes, A. (2008). Variation in mouse basolateral amygdala volume is associated with differences in stress reactivity and fear learning. Neuropsychopharmacology 33, 2595–2604. doi: 10.1038/sj.npp.1301665
Yoshida, S., Senba, E., Kubota, Y., Hagihira, S., Yoshiya, I., Emson, P. C., et al. (1990). Calcium-binding proteins calbindin and parvalbumin in the superficial dorsal horn of the rat spinal cord. Neuroscience 37, 839–848. doi: 10.1016/0306- 4522(90)90113-i
Zaborszky, L., Duque, A., Gielow, M., Gombkoto, P., Nadasdy, Z., and Somogyi,J. (2015). “Organization of the basal forebrain cholinergic projection system: specific or diffuse?,” in The Rat Nervous System, 4th Edn, ed. G. Paxinos (Amsterdam: Elsevier), 491–507.
Zaborszky, L., Van den Pol, A., and Gyengesi, E. (2012). “The basal forebrain cholinergic projection system in mice,” in The Mouse Nervous System, eds C. Watson, G. Paxinos, and L. Puelles (San Diego: Elsevier), 684–718.
Zahm, D. S., Grosu, S., Irving, J. C., and Williams, E. A. (2003). Discrimination of striatopallidum and extended amygdala in the rat: a role for parvalbumin immunoreactive neurons? Brain Res. 978, 141–154. doi: 10.1016/S0006- 8993(03)02801-4
Zangenehpour, S., and Chaudhuri, A. (2002). Differential induction and decay curves of c-fos and zif268 revealed through dual activity maps. Mol. Brain Res. 109, 221–225. doi: 10.1016/S0169-328X(02)00556-9