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Organization of connections between the amygdala, medial prefrontal cortex, and lateral hypothalamus: a single and double retrograde tracing study in rats

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Abstract

The amygdala and medial prefrontal cortex (mPFC) are highly interconnected telencephalic areas critical for cognitive processes, including associative learning and decision making. Both structures strongly innervate the lateral hypothalamus (LHA), an important component of the networks underlying the control of feeding and other motivated behaviors. The amygdala–prefrontal–lateral hypothalamic system is therefore well positioned to exert cognitive control over behavior. However, the organization of this system is not well defined, particularly the topography of specific circuitries between distinct cell groups within these complex, heterogeneous regions. This study used two retrograde tracers to map the connections from the amygdala (central and basolateral area nuclei) and mPFC to the LHA in detail, and to determine whether amygdalar pathways to the mPFC and to LHA originate from the same or different neurons. One tracer was placed into a distinct mPFC area (dorsal anterior cingulate, prelimbic, infralimbic, or rostromedial orbital), and the other into dorsal or ventral LHA. We report that the central nucleus and basolateral area of the amygdala send projections to distinct LHA regions, dorsal and ventral, respectively. The basolateral area, but not central nucleus, also sends substantial projections to the mPFC, topographically organized rostrocaudal to dorsoventral. The entire mPFC, in turn, projects to the LHA, providing a separate route for potential amygdalar influence following mPFC processing. Nearly all amygdalar projections to the mPFC and to the LHA originated from different neurons suggesting amygdala and amygdala–mPFC processing influence the LHA independently, and the balance of these parallel pathways ultimately controls motivated behaviors.

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Abbreviations

ACAd:

Anterior cingulate area, dorsal part

ACAv:

Anterior cingulate area, ventral part

BLA:

Basolateral amygdalar nucleus

BLAa:

Basolateral amygdalar nucleus, anterior part

BLAp:

Basolateral amygdalar nucleus, posterior part

BMA:

Basomedial amygdalar nucleus

BMAa:

Basomedial amygdalar nucleus, anterior part

BMAp:

Basomedial amygdalar nucleus, posterior part

CEA:

Central amygdalar nucleus

CEAc:

Central amygdalar nucleus, capsular part

CEAl:

Central amygdalar nucleus, lateral part

CEAm:

Central amygdalar nucleus, medial part

fx:

Fornix

ILA:

Infralimbic area

LA:

Lateral amygdalar nucleus

LHA:

Lateral hypothalamic area

LHAd:

Lateral hypothalamic area, dorsal region

LHAjd:

Lateral hypothalamic area, juxtadorsomedial region

LHAjvd:

Lateral hypothalamic area, juxtaventromedial region, dorsal zone

LHAjvv:

Lateral hypothalamic area, juxtaventromedial region, ventral zone

LHAs:

Lateral hypothalamic area, suprafornical region

mPFC:

Medial prefrontal cortex

ORB:

Orbital area

ORBl:

Orbital area, lateral part

ORBm:

Orbital area, medial part

ORBv:

Orbital area, ventral part

ORBvl:

Orbital area, ventrolateral part

PL:

Prelimbic area

TU:

Tuberal nucleus

References

  • Allen GV, Cechetto DF (1993) Functional and anatomical organization of cardiovascular pressor and depressor sites in the lateral hypothalamic area. II. Ascending projections. J Comp Neurol 330:421–438

    Article  CAS  PubMed  Google Scholar 

  • Anglada-Figueroa D, Quirk GJ (2005) Lesions of the basal amygdala block expression of conditioned fear but not extinction. J Neurosci 25:9680–9685

    Article  CAS  PubMed  Google Scholar 

  • Arvanitogiannis A, Tzschentke TM, Riscaldino L, Wise RA, Shizgal P (2000) Fos expression following self-stimulation of the medial prefrontal cortex. Behav Brain Res 107:123–132

    Article  CAS  PubMed  Google Scholar 

  • Ashwell R, Ito R (2014) Excitotoxic lesions of the infralimbic, but not prelimbic cortex facilitate reversal of appetitive discriminative context conditioning: the role of the infralimbic cortex in context generalization. Front Behav Neurosci 8:63

    Article  PubMed  PubMed Central  Google Scholar 

  • Berthoud HR, Münzberg H (2011) The lateral hypothalamus as integrator of metabolic and environmental needs: from electrical self-stimulation to opto-genetics. Physiol Behav 104:29–39

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Borgland SL et al (2009) Orexin A/hypocretin-1 selectively promotes motivation for positive reinforcers. J Neurosci 29:11215–11225

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Broberger C, De Lecea L, Sutcliffe JG, Hokfelt T (1998) Hypocretin/orexin- and melanin-concentrating hormone-expressing cells form distinct populations in the rodent lateral hypothalamus: relationship to the neuropeptide Y and agouti gene-related protein systems. J Comp Neurol 402:460–474

    Article  CAS  PubMed  Google Scholar 

  • Burgos-Robles A, Bravo-Rivera H, Quirk GJ (2013) Prelimbic and infralimbic neurons signal distinct aspects of appetitive instrumental behavior. PLoS ONE 8:e57575

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Cai H, Haubensak W, Anthony TE, Anderson DJ (2014) Central amygdala PKC-delta(+) neurons mediate the influence of multiple anorexigenic signals. Nat Neurosci 17:1240–1248

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Canteras NS, Swanson LW (1992) Projections of the ventral subiculum to the amygdala, septum, and hypothalamus: a PHAL anterograde tract-tracing study in the rat. J Comp Neurol 324:180–194

    Article  CAS  PubMed  Google Scholar 

  • Cason AM, Aston-Jones G (2013) Role of orexin/hypocretin in conditioned sucrose-seeking in rats. Psychopharmacology 226:155–165

    Article  CAS  PubMed  Google Scholar 

  • Cason AM, Aston-Jones G (2014) Role of orexin/hypocretin in conditioned sucrose-seeking in female rats. Neuropharmacology 86:97–102

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Cassell MD, Wright DJ (1986) Topography of projections from the medial prefrontal cortex to the amygdala in the rat. Brain Res Bull 17:321–333

    Article  CAS  PubMed  Google Scholar 

  • Cassell MD, Gray TS, Kiss JZ (1986) Neuronal architecture in the rat central nucleus of the amygdala: a cytological, hodological, and immunocytochemical study. J Comp Neurol 246:478–499

    Article  CAS  PubMed  Google Scholar 

  • Cenquizca LA, Swanson LW (2006) Analysis of direct hippocampal cortical field CA1 axonal projections to diencephalon in the rat. J Comp Neurol 497:101–114

    Article  PubMed  PubMed Central  Google Scholar 

  • Chefer VI, Wang R, Shippenberg TS (2011) Basolateral amygdala-driven augmentation of medial prefrontal cortex GABAergic neurotransmission in response to environmental stimuli associated with cocaine administration. Neuropsychopharmacology 36:2018–2029

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Choi DL, Davis JF, Fitzgerald ME, Benoit SC (2010) The role of orexin-A in food motivation, reward-based feeding behavior and food-induced neuronal activation in rats. Neuroscience 167:11–20

    Article  CAS  PubMed  Google Scholar 

  • Clegg DJ, Air EL, Woods SC, Seeley RJ (2002) Eating elicited by orexin-a, but not melanin-concentrating hormone, is opioid mediated. Endocrinology 143:2995–3000

    Article  CAS  PubMed  Google Scholar 

  • Cole S, Powell DJ, Petrovich GD (2013) Differential recruitment of distinct amygdalar nuclei across appetitive associative learning. Learn Mem 20:295–299

    Article  PubMed  PubMed Central  Google Scholar 

  • Cole S, Hobin MP, Petrovich GD (2015) Appetitive associative learning recruits a distinct network with cortical, striatal, and hypothalamic regions. Neuroscience 286:187–202

    Article  CAS  PubMed  Google Scholar 

  • Day HE, Curran EJ, Watson SJ Jr, Akil H (1999) Distinct neurochemical populations in the rat central nucleus of the amygdala and bed nucleus of the stria terminalis: evidence for their selective activation by interleukin-1beta. J Comp Neurol 413:113–128

    Article  CAS  PubMed  Google Scholar 

  • de Lecea L et al (1998) The hypocretins: hypothalamus-specific peptides with neuroexcitatory activity. Proc Natl Acad Sci USA 95:322–327

    Article  PubMed  PubMed Central  Google Scholar 

  • Dilgen J, Tejeda HA, O’Donnell P (2013) Amygdala inputs drive feedforward inhibition in the medial prefrontal cortex. J Neurophysiol 110:221–229

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Dong HW, Swanson LW (2003) Projections from the rhomboid nucleus of the bed nuclei of the stria terminalis: implications for cerebral hemisphere regulation of ingestive behaviors. J Comp Neurol 463:434–472

    Article  PubMed  Google Scholar 

  • Dong HW, Swanson LW (2004a) Organization of axonal projections from the anterolateral area of the bed nuclei of the stria terminalis. J Comp Neurol 468:277–298

    Article  PubMed  Google Scholar 

  • Dong HW, Swanson LW (2004b) Projections from bed nuclei of the stria terminalis, posterior division: implications for cerebral hemisphere regulation of defensive and reproductive behaviors. J Comp Neurol 471:396–433

    Article  PubMed  Google Scholar 

  • Dong HW, Swanson LW (2006a) Projections from bed nuclei of the stria terminalis, anteromedial area: cerebral hemisphere integration of neuroendocrine, autonomic, and behavioral aspects of energy balance. J Comp Neurol 494:142–178

    Article  PubMed  PubMed Central  Google Scholar 

  • Dong HW, Swanson LW (2006b) Projections from bed nuclei of the stria terminalis, dorsomedial nucleus: implications for cerebral hemisphere integration of neuroendocrine, autonomic, and drinking responses. J Comp Neurol 494:75–107

    Article  PubMed  PubMed Central  Google Scholar 

  • Dong HW, Swanson LW (2006c) Projections from bed nuclei of the stria terminalis, magnocellular nucleus: implications for cerebral hemisphere regulation of micturition, defecation, and penile erection. J Comp Neurol 494:108–141

    Article  PubMed  PubMed Central  Google Scholar 

  • Dong HW, Petrovich GD, Swanson LW (2000) Organization of projections from the juxtacapsular nucleus of the BST: a PHAL study in the rat. Brain Res 859:1–14

    Article  CAS  PubMed  Google Scholar 

  • Dong HW, Petrovich GD, Swanson LW (2001a) Topography of projections from amygdala to bed nuclei of the stria terminalis. Brain Res Rev 38:192–246

    Article  CAS  PubMed  Google Scholar 

  • Dong HW, Petrovich GD, Watts AG, Swanson LW (2001b) Basic organization of projections from the oval and fusiform nuclei of the bed nuclei of the stria terminalis in adult rat brain. J Comp Neurol 436:430–455

    Article  CAS  PubMed  Google Scholar 

  • Elmquist JK, Elias CF, Saper CB (1999) From lesions to leptin: hypothalamic control of food intake and body weight. Neuron 22:221–232

    Article  CAS  PubMed  Google Scholar 

  • Euston DR, Gruber AJ, McNaughton BL (2012) The role of medial prefrontal cortex in memory and decision making. Neuron 76:1057–1070

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Floresco SB, Tse MT (2007) Dopaminergic regulation of inhibitory and excitatory transmission in the basolateral amygdala–prefrontal cortical pathway. J Neurosci 27:2045–2057

    Article  CAS  PubMed  Google Scholar 

  • Floyd NS, Price JL, Ferry AT, Keay KA, Bandler R (2001) Orbitomedial prefrontal cortical projections to hypothalamus in the rat. J Comp Neurol 432:307–328

    Article  CAS  PubMed  Google Scholar 

  • Gabbott PL, Warner TA, Jays PR, Salway P, Busby SJ (2005) Prefrontal cortex in the rat: projections to subcortical autonomic, motor, and limbic centers. J Comp Neurol 492:145–177

    Article  PubMed  Google Scholar 

  • Gabbott PL, Warner TA, Busby SJ (2006) Amygdala input monosynaptically innervates parvalbumin immunoreactive local circuit neurons in rat medial prefrontal cortex. Neuroscience 139:1039–1048

    Article  CAS  PubMed  Google Scholar 

  • Gabbott PL, Warner TA, Brown J, Salway P, Gabbott T, Busby S (2012) Amygdala afferents monosynaptically innervate corticospinal neurones in rat medial prefrontal cortex (mPFC). J Comp Neurol 520:2440–2458

    Article  PubMed  Google Scholar 

  • Garcia R, Vouimba RM, Baudry M, Thompson RF (1999) The amygdala modulates prefrontal cortex activity relative to conditioned fear. Nature 402:294–296

    Article  CAS  PubMed  Google Scholar 

  • Goosens KA, Maren S (2001) Contextual and auditory fear conditioning are mediated by the lateral, basal, and central amygdaloid nuclei in rats. Learn Mem 8:148–155

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Goto M, Canteras NS, Burns G, Swanson LW (2005) Projections from the subfornical region of the lateral hypothalamic area. J Comp Neurol 493:412–438

    Article  PubMed  PubMed Central  Google Scholar 

  • Griffond B, Risold PY (2009) MCH and feeding behavior-interaction with peptidic network. Peptides 30:2045–2051

    Article  CAS  PubMed  Google Scholar 

  • Hahn JD (2010) Comparison of melanin-concentrating hormone and hypocretin/orexin peptide expression patterns in a current parceling scheme of the lateral hypothalamic zone. Neurosci Lett 468:12–17

    Article  CAS  PubMed  Google Scholar 

  • Hahn JD, Swanson LW (2010) Distinct patterns of neuronal inputs and outputs of the juxtaparaventricular and suprafornical regions of the lateral hypothalamic area in the male rat. Brain Res Rev 64:14–103

    Article  PubMed  PubMed Central  Google Scholar 

  • Hahn JD, Swanson LW (2012) Connections of the lateral hypothalamic area juxtadorsomedial region in the male rat. J Comp Neurol 520:1831–1890

    Article  PubMed  PubMed Central  Google Scholar 

  • Hahn JD, Swanson LW (2015) Connections of the juxtaventromedial region of the lateral hypothalamic area in the male rat. Front Syst Neurosci 9:66

    Article  PubMed  PubMed Central  Google Scholar 

  • Harris GC, Wimmer M, Aston-Jones G (2005) A role for lateral hypothalamic orexin neurons in reward seeking. Nature 437:556–559

    Article  CAS  PubMed  Google Scholar 

  • Haubensak W et al (2010) Genetic dissection of an amygdala microcircuit that gates conditioned fear. Nature 468:270–276

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Heidbreder CA, Groenewegen HJ (2003) The medial prefrontal cortex in the rat: evidence for a dorso-ventral distinction based upon functional and anatomical characteristics. Neurosci Biobehav Rev 27:555–579

    Article  PubMed  Google Scholar 

  • Holland PC, Petrovich GD, Gallagher M (2002) The effects of amygdala lesions on conditioned stimulus-potentiated eating in rats. Physiol Behav 76:117–129

    Article  CAS  PubMed  Google Scholar 

  • Hoover WB, Vertes RP (2007) Anatomical analysis of afferent projections to the medial prefrontal cortex in the rat. Brain Struct Funct 212:149–179

    Article  PubMed  Google Scholar 

  • Hoover WB, Vertes RP (2011) Projections of the medial orbital and ventral orbital cortex in the rat. J Comp Neurol 519:3766–3801

    Article  PubMed  Google Scholar 

  • Hurley KM, Herbert H, Moga MM, Saper CB (1991) Efferent projections of the infralimbic cortex of the rat. J Comp Neurol 308:249–276

    Article  CAS  PubMed  Google Scholar 

  • Jennings JH, Rizzi G, Stamatakis AM, Ung RL, Stuber GD (2013) The inhibitory circuit architecture of the lateral hypothalamus orchestrates feeding. Science 341:1517–1521

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Keefer SE, Reppucci CJ, Mayer, HS, Petrovich GD (2014) Plasticity within the basolateral amygdala pathways to the prelimbic cortex during Pavlovian appetitive conditioning. Program No. 650.11. 2014 Neuroscience Meeting Planner. Society for Neuroscience, Washington, DC (online)

  • Khan AM (2013) Controlling feeding behavior by chemical or gene-directed targeting in the brain: what’s so spatial about our methods? Front Neurosci 7:182

    Article  PubMed  PubMed Central  Google Scholar 

  • Kita H, Kitai ST (1990) Amygdaloid projections to the frontal cortex and the striatum in the rat. J Comp Neurol 298:40–49

    Article  CAS  PubMed  Google Scholar 

  • Kita H, Oomura Y (1982) An HRP study of the afferent connections to rat lateral hypothalamic region. Brain Res Bull 8:63–71

    Article  CAS  PubMed  Google Scholar 

  • Knapska E et al (2012) Functional anatomy of neural circuits regulating fear and extinction. Proc Natl Acad Sci USA 109:17093–17098

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Krettek JE, Price JL (1977a) The cortical projections of the mediodorsal nucleus and adjacent thalamic nuclei in the rat. J Comp Neurol 171:157–191

    Article  CAS  PubMed  Google Scholar 

  • Krettek JE, Price JL (1977b) Projections from the amygdaloid complex to the cerebral cortex and thalamus in the rat and cat. J Comp Neurol 172:687–722

    Article  CAS  PubMed  Google Scholar 

  • Krettek JE, Price JL (1978) Amygdaloid projections to subcortical structures within the basal forebrain and brainstem in the rat and cat. J Comp Neurol 178:225–254

    Article  CAS  PubMed  Google Scholar 

  • Lanciego JL, Wouterlood FG (2011) A half century of experimental neuroanatomical tracing. J Chem Neuroanat 42:157–183

    Article  PubMed  Google Scholar 

  • Land BB et al (2014) Medial prefrontal D1 dopamine neurons control food intake. Nat Neurosci 17:248–253

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Laviolette SR, Lipski WJ, Grace AA (2005) A subpopulation of neurons in the medial prefrontal cortex encodes emotional learning with burst and frequency codes through a dopamine D4 receptor-dependent basolateral amygdala input. J Neurosci 25:6066–6075

    Article  CAS  PubMed  Google Scholar 

  • Ledoux J (2012) Rethinking the emotional brain. Neuron 73:653–676

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Li H, Penzo MA, Taniguchi H, Kopec CD, Huang ZJ, Li B (2013) Experience-dependent modification of a central amygdala fear circuit. Nat Neurosci 16:332–339

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Likhtik E, Paz R (2015) Amygdala–prefrontal interactions in (mal)adaptive learning. Trends Neurosci 38:158–166

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Maeng LY, Shors TJ (2013) The stressed female brain: neuronal activity in the prelimbic but not infralimbic region of the medial prefrontal cortex suppresses learning after acute stress. Front Neural Circuits 7:198

    Article  PubMed  PubMed Central  Google Scholar 

  • Marchant NJ, Densmore VS, Osborne PB (2007) Coexpression of prodynorphin and corticotrophin-releasing hormone in the rat central amygdala: evidence of two distinct endogenous opioid systems in the lateral division. J Comp Neurol 504:702–715

    Article  CAS  PubMed  Google Scholar 

  • Maren S, Aharonov G, Fanselow MS (1996) Retrograde abolition of conditional fear after excitotoxic lesions in the basolateral amygdala of rats: absence of a temporal gradient. Behav Neurosci 110:718–726

    Article  CAS  PubMed  Google Scholar 

  • Martinez RC et al (2013) Active vs. reactive threat responding is associated with differential c-Fos expression in specific regions of amygdala and prefrontal cortex. Learn Mem 20:446–452

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • McDonald AJ (1987) Organization of amygdaloid projections to the mediodorsal thalamus and prefrontal cortex: a fluorescence retrograde transport study in the rat. J Comp Neurol 262:46–58

    Article  CAS  PubMed  Google Scholar 

  • McDonald AJ (1991) Organization of amygdaloid projections to the prefrontal cortex and associated striatum in the rat. Neuroscience 44:1–14

    Article  CAS  PubMed  Google Scholar 

  • McDonald AJ (1992) Projection neurons of the basolateral amygdala: a correlative Golgi and retrograde tract tracing study. Brain Res Bull 28:179–185

    Article  CAS  PubMed  Google Scholar 

  • McDonald AJ (1998) Cortical pathways to the mammalian amygdala. Prog Neurobiol 55:257–332

    Article  CAS  PubMed  Google Scholar 

  • McDonald AJ (2003) Is there an amygdala and how far does it extend? Ann NY Acad Sci 985(1):1–21

    Article  PubMed  Google Scholar 

  • Mena JD, Sadeghian K, Baldo BA (2011) Induction of hyperphagia and carbohydrate intake by mu-opioid receptor stimulation in circumscribed regions of frontal cortex. J Neurosci 31:3249–3260

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Mena JD, Selleck RA, Baldo BA (2013) Mu-opioid stimulation in rat prefrontal cortex engages hypothalamic orexin/hypocretin-containing neurons, and reveals dissociable roles of nucleus accumbens and hypothalamus in cortically driven feeding. J Neurosci 33:18540–18552

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Mendoza J, Sanio C, Chaudhri N (2014) Inactivating the infralimbic but not prelimbic medial prefrontal cortex facilitates the extinction of appetitive Pavlovian conditioning in Long–Evans rats. Neurobiol Learn Mem 118:198–208

    Article  PubMed  Google Scholar 

  • Nahon JL, Presse F, Bittencourt JC, Sawchenko PE, Vale W (1989) The rat melanin-concentrating hormone messenger ribonucleic acid encodes multiple putative neuropeptides coexpressed in the dorsolateral hypothalamus. Endocrinology 125:2056–2065

    Article  CAS  PubMed  Google Scholar 

  • Nair SG, Golden SA, Shaham Y (2008) Differential effects of the hypocretin 1 receptor antagonist SB 334867 on high-fat food self-administration and reinstatement of food seeking in rats. Br J Pharmacol 154:406–416

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Nakamura S, Tsumori T, Yokota S, Oka T, Yasui Y (2009) Amygdaloid axons innervate melanin-concentrating hormone- and orexin-containing neurons in the mouse lateral hypothalamus. Brain Res 1278:66–74

    Article  CAS  PubMed  Google Scholar 

  • Niu JG, Yokota S, Tsumori T, Oka T, Yasui Y (2012) Projections from the anterior basomedial and anterior cortical amygdaloid nuclei to melanin-concentrating hormone-containing neurons in the lateral hypothalamus of the rat. Brain Res 1479:31–43

    Article  CAS  PubMed  Google Scholar 

  • Ono T, Luiten PGM, Nishijo H, Fukuda M, Nishino H (1985) Topographic organization of projections from the amygdala to the hypothalamus of the rat. Neurosci Res 2:221–238

    Article  CAS  PubMed  Google Scholar 

  • Perez-Jaranay JM, Vives F (1991) Electrophysiological study of the response of medial prefrontal cortex neurons to stimulation of the basolateral nucleus of the amygdala in the rat. Brain Res 564:97–101

    Article  CAS  PubMed  Google Scholar 

  • Petrovich GD (2013) Forebrain networks and the control of feeding by environmental learned cues. Physiol Behav 121:10–18

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Petrovich GD, Swanson LW (1997) Projections from the lateral part of the central amygdalar nucleus to the postulated fear conditioning circuit. Brain Res 763:247–254

    Article  CAS  PubMed  Google Scholar 

  • Petrovich GD, Risold PY, Swanson LW (1996) Organization of projections from the basomedial nucleus of the amygdala: a PHAL study in the rat. J Comp Neurol 374:387–420

    Article  CAS  PubMed  Google Scholar 

  • Petrovich GD, Canteras NS, Swanson LW (2001) Combinatorial amygdalar inputs to hippocampal domains and hypothalamic behavior systems. Brain Res Rev 38:247–289

    Article  CAS  PubMed  Google Scholar 

  • Petrovich GD, Holland PC, Gallagher M (2005) Amygdalar and prefrontal pathways to the lateral hypothalamus are activated by a learned cue that stimulates eating. J Neurosci 25:8295–8302

    Article  CAS  PubMed  Google Scholar 

  • Petrovich GD, Ross CA, Gallagher M, Holland PC (2007a) Learned contextual cue potentiates eating in rats. Physiol Behav 90:362–367

    Article  CAS  PubMed  Google Scholar 

  • Petrovich GD, Ross CA, Holland PC, Gallagher M (2007b) Medial prefrontal cortex is necessary for an appetitive contextual conditioned stimulus to promote eating in sated rats. J Neurosci 27:6436–6441

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Petrovich GD, Ross CA, Mody P, Holland PC, Gallagher M (2009) Central, but not basolateral, amygdala is critical for control of feeding by aversive learned cues. J Neurosci 29:15205–15212

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Petrovich GD, Hobin MP, Reppucci CJ (2012) Selective Fos induction in hypothalamic orexin/hypocretin, but not melanin-concentrating hormone neurons, by a learned food-cue that stimulates feeding in sated rats. Neuroscience 224:70–80

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Pitkänen A, Savander V, LeDoux JE (1997) Organization of intra-amygdaloid circuitries in the rat: an emerging framework for understanding functions of the amygdala. Trends Neurosci 20:517–523

    Article  PubMed  Google Scholar 

  • Risold PY, Swanson LW (1996) Structural evidence for functional domains in the rat hippocampus. Science 272:1484–1486

    Article  CAS  PubMed  Google Scholar 

  • Roberts GW, Woodhams PL, Polak JM, Crow TJ (1982) Distribution of neuropeptides in the limbic system of the rat: the amygdaloid complex. Neuroscience 7:99–131

    Article  CAS  PubMed  Google Scholar 

  • Sakurai T et al (1998) Orexins and orexin receptors: a family of hypothalamic neuropeptides and G protein-coupled receptors that regulate feeding behavior. Cell 92:573–585

    Article  CAS  PubMed  Google Scholar 

  • Saper CB (1985) Organization of cerebral cortical afferent systems in the rat. II. Hypothalamocortical projections. J Comp Neurol 237:21–46

    Article  CAS  PubMed  Google Scholar 

  • Savander V, Go CG, LeDoux JE, Pitkänen A (1995) Intrinsic connections of the rat amygdaloid complex: projections originating in the basal nucleus. J Comp Neurol 361:345–368

    Article  CAS  PubMed  Google Scholar 

  • Senn V et al (2014) Long-range connectivity defines behavioral specificity of amygdala neurons. Neuron 81:428–437

    Article  CAS  PubMed  Google Scholar 

  • Sesack SR, Deutch AY, Roth RH, Bunney BS (1989) Topographical organization of the efferent projections of the medial prefrontal cortex in the rat: an anterograde tract-tracing study with Phaseolus vulgaris leucoagglutinin. J Comp Neurol 290:213–242

    Article  CAS  PubMed  Google Scholar 

  • Seymour B, Dolan R (2008) Emotion, decision making, and the amygdala. Neuron 58:662–671

    Article  CAS  PubMed  Google Scholar 

  • Sherwood A, Holland PC, Adamantidis A, Johnson AW (2015) Deletion of melanin concentrating hormone receptor-1 disrupts overeating in the presence of food cues. Physiol Behav (in press)

  • Sierra-Mercado D, Padilla-Coreano N, Quirk GJ (2011) Dissociable roles of prelimbic and infralimbic cortices, ventral hippocampus, and basolateral amygdala in the expression and extinction of conditioned fear. Neuropsychopharmacology 36:529–538

    Article  PubMed  Google Scholar 

  • Simmons DM, Swanson LW (1993) The Nissl stain. Neurosci Protoc. 050-12-01-07

  • Sotres-Bayon F, Sierra-Mercado D, Pardilla-Delgado E, Quirk GJ (2012) Gating of fear in prelimbic cortex by hippocampal and amygdala inputs. Neuron 76:804–812

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Stanley BG, Urstadt KR, Charles JR, Kee T (2011) Glutamate and GABA in lateral hypothalamic mechanisms controlling food intake. Physiol Behav 104:40–46

    Article  CAS  PubMed  Google Scholar 

  • Stefanik MT, Kalivas PW (2013) Optogenetic dissection of basolateral amygdala projections during cue-induced reinstatement of cocaine seeking. Front Behav Neurosci 7:213

    Article  PubMed  PubMed Central  Google Scholar 

  • Swanson LW (2000) Cerebral hemisphere regulation of motivated behavior. Brain Res 886:113–164

    Article  CAS  PubMed  Google Scholar 

  • Swanson LW (2004) Brain maps III: structure of the rat brain. An atlas with printed and electronic templates for data, models, and schematics, 3rd rev. edn. Elsevier, Academic Press, Amsterdam

  • Swanson LW (2005) Anatomy of the soul as reflected in the cerebral hemispheres: neural circuits underlying voluntary control of basic motivated behaviors. J Comp Neurol 493:122–131

    Article  PubMed  Google Scholar 

  • Swanson LW, Petrovich GD (1998) What is the amygdala? Trends Neurosci 21:323–331

    Article  CAS  PubMed  Google Scholar 

  • Swanson LW, Sanchez-Watts G, Watts AG (2005) Comparison of melanin-concentrating hormone and hypocretin/orexin mRNA expression patterns in a new parceling scheme of the lateral hypothalamic zone. Neurosci Lett 387:80–84

    Article  CAS  PubMed  Google Scholar 

  • Takagishi M, Chiba T (1991) Efferent projections of the infralimbic (area 25) region of the medial prefrontal cortex in the rat: an anterograde tracer PHA-L study. Brain Res 566:26–39

    Article  CAS  PubMed  Google Scholar 

  • Toth M, Fuzesi T, Halasz J, Tulogdi A, Haller J (2010) Neural inputs of the hypothalamic “aggression area” in the rat. Behav Brain Res 215:7–20

    Article  PubMed  Google Scholar 

  • Tsujino N, Sakurai T (2009) Orexin/hypocretin: a neuropeptide at the interface of sleep, energy homeostasis, and reward system. Pharmacol Rev 61:162–176

    Article  CAS  PubMed  Google Scholar 

  • Van De Werd HJ, Uylings HB (2008) The rat orbital and agranular insular prefrontal cortical areas: a cytoarchitectonic and chemoarchitectonic study. Brain Struct Funct 212:387–401

    Article  Google Scholar 

  • Vertes RP (2004) Differential projections of the infralimbic and prelimbic cortex in the rat. Synapse 51:32–58

    Article  CAS  PubMed  Google Scholar 

  • Villalobos J, Ferssiwi A (1987) The differential ascending projections from the anterior, central and posterior regions of the lateral hypothalamic area: an autoradiographic study. Neurosci Lett 81:89–94

    Article  CAS  PubMed  Google Scholar 

  • Wise RA (1974) Lateral hypothalamic electrical stimulation: does it make animals ‘hungry’? Brain Res 67:187–209

    Article  CAS  PubMed  Google Scholar 

  • Wray S, Hoffman GE (1983) Organization and interrelationship of neuropeptides in the central amygdaloid nucleus of the rat. Peptides 4:525–541

    Article  CAS  PubMed  Google Scholar 

  • Yoshida K, McCormack S, Espana RA, Crocker A, Scammell TE (2006) Afferents to the orexin neurons of the rat brain. J Comp Neurol 494:845–861

    Article  PubMed  PubMed Central  Google Scholar 

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Acknowledgments

We thank Meghana Kuthyar and Heather Mayer for technical assistance. This research was supported in part by National Institute of Health grant DK085721 to G.D.P.

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Correspondence to Gorica D. Petrovich.

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All applicable international, national, and institutional guidelines for the care and use of animals were followed.

All procedures performed in this study involving animals were in accordance with the ethical standards of the Boston College Institutional Animal Care and Use Committee.

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Reppucci, C.J., Petrovich, G.D. Organization of connections between the amygdala, medial prefrontal cortex, and lateral hypothalamus: a single and double retrograde tracing study in rats. Brain Struct Funct 221, 2937–2962 (2016). https://doi.org/10.1007/s00429-015-1081-0

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  • DOI: https://doi.org/10.1007/s00429-015-1081-0

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