[Abbadie C, Pan YX, Pasternak GW. Differential distribution in rat brain of mu opioid receptor carboxy terminal splice variants MOR-1C-like and MOR-1-like immunoreactivity: evidence for region-specific processing. J Comp Neurol 419, 244-256, 2000.10.1002/(SICI)1096-9861(20000403)419:2<244::AID-CNE8>3.0.CO;2-R]Search in Google Scholar
[Adametz J, O’Leary JL. Experimental mutism resulting from periaqueductal lesions in cats. Neurology 9, 636-642, 1959.10.1212/WNL.9.10.63613791737]Open DOISearch in Google Scholar
[Adolphs R. The neurobiology of social cognition. Curr Opin Neurobiol 11, 231-239, 2001.10.1016/S0959-4388(00)00202-6]Search in Google Scholar
[Anderzhanova E, Kirmeier T, Wotjak CT. Animal models in psychiatric research: The RDoC system as a new framework for endophenotype-oriented translational neuroscience. Neurobiol Stress 7, 47-56, 2017.10.1016/j.ynstr.2017.03.003]Search in Google Scholar
[Apfelbach R, Blanchard CD, Blanchard RJ, Hayes RA, McGregor IS. The effects of predator odors in mammalian prey species: a review of field and laboratory studies. Neurosci Biobehav Rev 29, 1123-1144, 2005.10.1016/j.neubiorev.2005.05.005]Search in Google Scholar
[Asan E, Steinke M, Lesch KP. Serotonergic innervation of the amygdala: targets, receptors, and implications for stress and anxiety. Histochem Cell Biol 139, 785-813, 2013.10.1007/s00418-013-1081-1]Search in Google Scholar
[Bales KL. Parenting in Animals. Curr Opin Psychol 15, 93-98, 2017.10.1016/j.copsyc.2017.02.026]Search in Google Scholar
[Bandler R, Shipley MT. Columnar organization in the midbrain periaqueductal gray: modules for emotional expression? Trends Neurosci 17, 379-389, 1994.10.1016/0166-2236(94)90047-7]Open DOISearch in Google Scholar
[Bandler R, Keay KA, Floyd N, Price J. Central circuits mediating patterned autonomic activity during active vs. passive emotional coping. Brain Res Bull 53, 95-104, 2000.10.1016/S0361-9230(00)00313-0]Search in Google Scholar
[Barba-Muller E, Craddock S, Carmona S, Hoekzema E. Brain plasticity in pregnancy and the postpartum period: links to maternal caregiving and mental health. Arch Womens Ment Health 2018.10.1007/s00737-018-0889-z]Search in Google Scholar
[Bartsch T, Knight YE, Goadsby PJ. Activation of 5-HT(1B/1D) receptor in the periaqueductal gray inhibits nociception. Ann Neurol 56, 371-381, 2004.10.1002/ana.20193]Search in Google Scholar
[Basbaum AI, Fields HL. Endogenous pain control systems: brainstem spinal pathways and endorphin circuitry. Annu Rev Neurosci 7, 309-338, 1984.10.1146/annurev.ne.07.030184.001521]Open DOISearch in Google Scholar
[Baslow MH. Evidence supporting a role for N-acetyl-L-aspartate as a molecular water pump in myelinated neurons in the central nervous system. An analytical review. Neurochem Int 40, 295-300, 2002.1179245810.1016/S0197-0186(01)00095-X]Search in Google Scholar
[Beckett S, Marsden CA. The effect of central and systemic injection of the 5-HT1A receptor agonist 8-OHDPAT and the 5-HT1A receptor antagonist WAY100635 on periaqueductal grey-induced defence behaviour. J Psychopharmacol 11, 35-40, 1997.10.1177/0269881197011001119097891]Search in Google Scholar
[Benarroch EE. Periaqueductal gray: an interface for behavioral control. Neurology 78, 210-217, 2012.10.1212/WNL.0b013e31823fcdee22249496]Open DOISearch in Google Scholar
[Benedetti F, Carlino E, Pollo A. How placebos change the patient’s brain. Neuropsychopharmacology 36, 339-354, 2011.10.1038/npp.2010.81305551520592717]Open DOISearch in Google Scholar
[Bindra D. Emotion and behavior theory: current research in historical perspective. In Physiological Correlates of Emotion, Reed Elsevier. ed., Perry Black. Academic Press, USA, 1970.10.1016/B978-0-12-102850-3.50007-4]Search in Google Scholar
[Bingel U, Lorenz J, Schoell E, Weiller C, Buchel C. Mechanisms of placebo analgesia: rACC recruitment of a subcortical antinociceptive network. Pain 120, 8-15, 2006.10.1016/j.pain.2005.08.02716364549]Search in Google Scholar
[Blakemore RL, Rieger SW, Vuilleumier P. Negative emotions facilitate isometric force through activation of prefrontal cortex and periaqueductal gray. Neuroimage 124, 627-640, 2016.10.1016/j.neuroimage.2015.09.02926400014]Search in Google Scholar
[Blanchard C, Blanchard R, Fellous JM, Guimaraes FS, Irwin W, Ledoux JE, McGaugh JL, Rosen JB, Schenberg LC, Volchan E, Da Cunha C. The brain decade in debate: III. Neurobiology of emotion. Braz J Med Biol Res 34, 283-293, 2001.10.1590/S0100-879X200100030000111262578]Open DOISearch in Google Scholar
[Bodnar RJ. Endogenous opiates and behavior: 2011. Peptides 38, 463-522, 2012.10.1016/j.peptides.2012.09.027]Search in Google Scholar
[Boissy A, Arnould C, Chaillou E, Desire L, Duvaux-Ponter C, Greiveldinger L, Leterrier C, Richard S, Roussel S, Saint-Dizier H, Meunier-Salaun MC, Valance D, Veissier I. Emotions and cognition: A new approach to animal welfare. Anim Welf 16, 37-43, 2007.]Search in Google Scholar
[Bombardi C. Neuronal localization of the 5-HT2 receptor family in the amygdaloid complex. Front Pharmacol 5, 68, 2014.10.3389/fphar.2014.00068]Search in Google Scholar
[Brent LJ, Chang SW, Gariepy JF, Platt ML. The neuroethology of friendship. Ann N Y Acad Sci 1316, 1-17, 2014.10.1111/nyas.12315]Search in Google Scholar
[Buhle JT, Kober H, Ochsner KN, Mende-Siedlecki P, Weber J, Hughes BL, Kross E, Atlas LY, McRae K, Wager TD. Common representation of pain and negative emotion in the midbrain periaqueductal gray. Soc Cogn Affect Neurosci 8, 609-616, 2013.10.1093/scan/nss038]Search in Google Scholar
[Buonanotte F, Schurrer C, Carpinella M, Surur A, Marangoni A, Palacio S, Forteza M, Fernandez R, Enders J. [Alteration of the antinociceptive systems in chronic daily headaches]. Rev Neurol 43, 263-267, 2006.1694142310.33588/rn.4305.2005706]Search in Google Scholar
[Campos AC, de Paula Soares V, Carvalho MC, Ferreira FR, Vicente MA, Brandao ML, Zuardi AW, Zangrossi H Jr, Guimaraes FS. Involvement of serotonin-mediated neurotransmission in the dorsal periaqueductal gray matter on cannabidiol chronic effects in panic-like responses in rats. Psychopharmacology (Berl) 226, 13-24, 2013.10.1007/s00213-012-2878-7]Search in Google Scholar
[Cannon WB. The James-Lange theory of emotions: A critical examination and an alternative theory. Am J Psychol 39, 106-124, 1927.10.2307/1415404]Search in Google Scholar
[Carrive P, Leung P, Harris J, Paxinos G. Conditioned fear to context is associated with increased Fos expression in the caudal ventrolateral region of the midbrain periaqueductal gray. Neuroscience 78, 165-177, 1997.10.1016/S0306-4522(97)83047-39135098]Open DOISearch in Google Scholar
[Carstens E, Hartung M, Stelzer B, Zimmermann M. Suppression of a hind limb flexion withdrawal reflex by microinjection of glutamate or morphine into the periaqueductal gray in the rat. Pain 43, 105-112, 1990.198053510.1016/0304-3959(90)90055-I]Search in Google Scholar
[Chiou RJ, Kuo CC, Yen CT. Comparisons of terminal densities of cardiovascular function-related projections from the amygdala subnuclei. Auton Neurosci 181, 21-30, 2014.10.1016/j.autneu.2013.12.00224412638]Search in Google Scholar
[Clements JR, Beitz AJ, Fletcher TF, Mullett MA. Immunocytochemical localization of serotonin in the rat periaqueductal gray: a quantitative light and electron microscopic study. J Comp Neurol 236, 60-70, 1985.10.1002/cne.902360106]Search in Google Scholar
[Coutinho MR, Menescal-de-Oliveira L. Role of homocysteic acid in the guinea pig (Cavia porcellus) anterior cingulate cortex in tonic immobility and the influence of NMDA receptors on the dorsal PAG. Behav Brain Res 208, 237-242, 2010.10.1016/j.bbr.2009.11.047]Search in Google Scholar
[Dampney R. Emotion and the cardiovascular system: Postulated role of inputs from the medial prefrontal cortex to the dorsolateral periaqueductal gray. Front Neurosci 12, 343, 2018.10.3389/fnins.2018.00343]Search in Google Scholar
[Dantzer R. Les emotions. Presses Universitaires de France,”Que sais-je?”, 2002a.10.3917/puf.dantz.2002.01]Search in Google Scholar
[Dantzer R. Can farm animal welfare be understood without taking into account the issues of emotion and cognition? J Anim Sci 80, E1-E9, 2002b.]Search in Google Scholar
[Darwin C. The Expression of the Emotions in Man and Animals. 1872.10.1037/10001-000]Open DOISearch in Google Scholar
[Davis PJ, Zhang SP, Winkworth A, Bandler R. Neural control of vocalization: respiratory and emotional influences. J Voice 10, 23-38, 1996.10.1016/S0892-1997(96)80016-6]Search in Google Scholar
[de Almeida J, Palacios JM, Mengod G. Distribution of 5-HT and DA receptors in primate prefrontal cortex: implications for pathophysiology and treatment. Prog Brain Res 172, 101-115, 2008.10.1016/S0079-6123(08)00905-9]Search in Google Scholar
[Decety J, Michalska KJ, Akitsuki Y. Who caused the pain? An fMRI investigation of empathy and intentionality in children. Neuropsychologia 46, 2607-2614, 2008.10.1016/j.neuropsychologia.2008.05.0261857326618573266]Open DOISearch in Google Scholar
[Decety J, Michalska KJ, Akitsuki Y, Lahey BB. Atypical empathic responses in adolescents with aggressive conduct disorder: a functional MRI investigation. Biol Psychol 80, 203-211, 2009.1894023010.1016/j.biopsycho.2008.09.004281931018940230]Search in Google Scholar
[Decety J, Echols S, Correll J. The blame game: the effect of responsibility and social stigma on empathy for pain. J Cogn Neurosci 22, 985-997, 2010.10.1162/jocn.2009.2126619425830]Search in Google Scholar
[de Menezes RC, Zaretsky DV, Fontes MA, DiMicco JA. Microinjection of muscimol into caudal periaqueductal gray lowers body temperature and attenuates increases in temperature and activity evoked from the dorsomedial hypothalamus. Brain Res 1092, 129-137, 2006.10.1016/j.brainres.2006.03.080]Search in Google Scholar
[De Oca BM, DeCola JP, Maren S, Fanselow MS. Distinct regions of the periaqueductal gray are involved in the acquisition and expression of defensive responses. J Neurosci 18, 3426-3432, 1998.10.1523/JNEUROSCI.18-09-03426.1998]Open DOISearch in Google Scholar
[Depaulis A, Bandler R, Vergnes M. Characterization of pretentorial periaqueductal gray matter neurons mediating intraspecific defensive behaviors in the rat by microinjections of kainic acid. Brain Res 486, 121-132, 1989.10.1016/0006-8993(89)91284-5]Search in Google Scholar
[DeSantana JM, Da Silva LF, De Resende MA, Sluka KA. Transcutaneous electrical nerve stimulation at both high and low frequencies activates ventrolateral periaqueductal grey to decrease mechanical hyperalgesia in arthritic rats. Neuroscience 163, 1233-1241, 2009.10.1016/j.neuroscience.2009.06.056395525919576962]Search in Google Scholar
[Dunckley P, Wise RG, Fairhurst M, Hobden P, Aziz Q, Chang L, Tracey I. A comparison of visceral and somatic pain processing in the human brainstem using functional magnetic resonance imaging. J Neurosci 25, 7333-7341, 2005.10.1523/JNEUROSCI.1100-05.200516093383672529716093383]Open DOISearch in Google Scholar
[Eippert F, Bingel U, Schoell ED, Yacubian J, Klinger R, Lorenz J, Buchel C. Activation of the opioidergic descending pain control system underlies placebo analgesia. Neuron 63, 533-543, 2009.1970963410.1016/j.neuron.2009.07.01419709634]Search in Google Scholar
[Ezra M, Faull OK, Jbabdi S, Pattinson KT. Connectivity-based segmentation of the periaqueductal gray matter in human with brainstem optimized diffusion MRI. Hum Brain Mapp 36, 3459-3471, 2015.10.1002/hbm.22855475513526138504]Search in Google Scholar
[Fairhurst M, Wiech K, Dunckley P, Tracey I. Anticipatory brainstem activity predicts neural processing of pain in humans. Pain 128, 101-110, 2007.10.1016/j.pain.2006.09.00117070996]Search in Google Scholar
[Fairhurst M, Fairhurst K, Berna C, Tracey I. An fMRI study exploring the overlap and differences between neural representations of physical and recalled pain. PLoS One 7, e48711, 2012.2311909310.1371/journal.pone.0048711348531723119093]Search in Google Scholar
[Farmer DG, Bautista TG, Jones SE, Stanic D, Dutschmann M. The midbrain periaqueductal grey has no role in the generation of the respiratory motor pattern, but provides command function for the modulation of respiratory activity. Respir Physiol Neurobiol 204, 14-20, 2014.10.1016/j.resp.2014.07.01125058161]Search in Google Scholar
[Faull OK, Jenkinson M, Clare S, Pattinson KT. Functional subdivision of the human periaqueductal grey in respiratory control using 7 tesla fMRI. Neuroimage 113, 356-364, 2015.10.1016/j.neuroimage.2015.02.026]Search in Google Scholar
[Figueira RJ, Peabody MF, Lonstein JS. Oxytocin receptor activity in the ventrocaudal periaqueductal gray modulates anxiety-related behavior in postpartum rats. Behav Neurosci 122, 618-628, 2008.10.1037/0735-7044.122.3.618]Search in Google Scholar
[Freeman SM, Walum H, Inoue K, Smith AL, Goodman MM, Bales KL, Young LJ. Neuroanatomical distribution of oxytocin and vasopressin 1a receptors in the socially monogamous coppery titi monkey (Callicebus cupreus). Neuroscience 273, 12-23, 2014.10.1016/j.neuroscience.2014.04.055]Search in Google Scholar
[Furl N. Structural and effective connectivity reveals potential network-based influences on category-sensitive visual areas. Front Hum Neurosci 9, 253, 2015.10.3389/fnhum.2015.00253]Search in Google Scholar
[Garcia-Larrea L, Peyron R. Pain matrices and neuropathic pain matrices: a review. Pain 154 (Suppl 1), S29-S43, 2013.10.1016/j.pain.2013.09.001]Search in Google Scholar
[Gaudin S, Chaillou E, Wycke MA, Cornilleau F, Moussu C, Calandreau L, Laine AL, Nowak R. All bonds are not alike: A psychoendocrine evaluation of infant attachment. Dev Psychobiol 60, 90-103. 2018.10.1002/dev.21552]Search in Google Scholar
[Gregg TR, Siegel A. Brain structures and neurotransmitters regulating aggression in cats: implications for human aggression. Prog Neuropsychopharmacol Biol Psychiatry. 25, 91-140, 2001.10.1016/S0278-5846(00)00150-0]Open DOISearch in Google Scholar
[Guesdon V, Meurisse M, Chesneau D, Picard S, Levy F, Chaillou E. Behavioral and endocrine evaluation of the stressfulness of single-pen housing compared to group-housing and social isolation conditions. Physiol Behav 147, 63-70, 2015.10.1016/j.physbeh.2015.04.01325865708]Search in Google Scholar
[Harper DE, Ichesco E, Schrepf A, Hampson JP, Clauw DJ, Schmidt-Wilcke T, Harris RE, Harte SE. Resting functional connectivity of the periaqueductal gray is associated with normal inhibition and pathological facilitation in conditioned pain modulation. J Pain 19, 635 e1-635 e15, 2018.2936060810.1016/j.jpain.2018.01.001597206729360608]Search in Google Scholar
[Holstege G, Huynh HK. Brain circuits for mating behavior in cats and brain activations and de-activations during sexual stimulation and ejaculation and orgasm in humans. Horm Behav 59, 702-707, 2011.10.1016/j.yhbeh.2011.02.00821352827]Search in Google Scholar
[Hopkins DA, Holstege G. Amygdaloid projections to the mesencephalon, pons and medulla oblongata in the cat. Exp Brain Res 32, 529-547, 1978.10.1007/BF00239551]Search in Google Scholar
[Hosobuchi Y. Dorsal periaqueductal gray-matter stimulation in humans. Pacing Clin Electrophysiol 10, 213-216, 1987.10.1111/j.1540-8159.1987.tb05951.x]Search in Google Scholar
[Jansen AS, Farkas E, Mac Sams J, Loewy AD. Local connections between the columns of the periaqueductal gray matter: a case for intrinsic neuromodulation. Brain Res 784, 329-336, 1998.10.1016/S0006-8993(97)01293-6]Search in Google Scholar
[Jurgens U. The role of the periaqueductal grey in vocal behaviour. Behav Brain Res 62, 107-117, 1994.10.1016/0166-4328(94)90017-5]Search in Google Scholar
[Keay KA, Bandler R. Distinct central representations of inescapable and escapable pain: observations and speculation. Exp Physiol 87, 275-279, 2002.10.1113/eph870235511856974]Search in Google Scholar
[Kelly AH, Beaton LE, Magoun HW. A midbrain mechanism for facio-vocal activity. J Neurophysiol 9, 181-189, 1946.10.1152/jn.1946.9.3.1812102816121028161]Open DOISearch in Google Scholar
[Kirouac G. Cognition et emotions. Les presses de l’universite Laval, 223, 1998.]Search in Google Scholar
[Klein MO, Cruz Ade M, Machado FC, Picolo G, Canteras NS, Felicio LF. Periaqueductal gray mu and kappa opioid receptors determine behavioral selection from maternal to predatory behavior in lactating rats. Behav Brain Res 274, 62-72, 2014.10.1016/j.bbr.2014.08.00825116253]Search in Google Scholar
[Kyuhou S, Gemba H. Two vocalization-related subregions in the midbrain periaqueductal gray of the guinea pig. Neuroreport 9, 1607-1610, 1998.10.1097/00001756-199805110-0006496314749631474]Open DOISearch in Google Scholar
[La Cesa S, Tinelli E, Toschi N, Di Stefano G, Collorone S, Aceti A, Francia A, Cruccu G, Truini A, Caramia F. fMRI pain activation in the periaqueductal gray in healthy volunteers during the cold pressor test. Magn Reson Imaging 32, 236-240, 2014.10.1016/j.mri.2013.12.00324468081]Open DOISearch in Google Scholar
[Laprairie JL, Murphy AZ. Neonatal injury alters adult pain sensitivity by increasing opioid tone in the periaqueductal gray. Front Behav Neurosci 3, 31, 2009.10.3389/neuro.08.031.2009276678319862348]Search in Google Scholar
[LeDoux JE, Iwata J, Cicchetti P, Reis DJ. Different projections of the central amygdaloid nucleus mediate autonomic and behavioral correlates of conditioned fear. J Neurosci 8, 2517-2529, 1988.285484210.1523/JNEUROSCI.08-07-02517.1988]Search in Google Scholar
[Lei J, Sun T, Lumb BM, You HJ. Roles of the periaqueductal gray in descending facilitatory and inhibitory controls of intramuscular hypertonic saline induced muscle nociception. Exp Neurol 257, 88-94, 2014.10.1016/j.expneurol.2014.04.019]Search in Google Scholar
[Leman S, Dielenberg RA, Carrive P. Effect of dorsal periaqueductal gray lesion on cardiovascular and behavioural responses to contextual conditioned fear in rats. Behav Brain Res 143, 169-176, 2003.10.1016/S0166-4328(03)00033-0]Search in Google Scholar
[Leventhal H, Scherer K. The relationship of emotion to cognition: A functional approach to a semantic controversy. Cogn Emot 1, 3-28, 1987.10.1080/02699938708408361]Search in Google Scholar
[Leventhal H, Patrick-Miller L. Emotions and physical illness: Causes and indicators of vulnerability. Handbook of Emotions, 2nd ed. M. Lewis & J. M. Haviland-Jones, New York, Guilford Press, 2000.]Search in Google Scholar
[Levy F. Neurobiological mechanisms involved in recognition of olfactory signature of the young in sheep. J Soc Biol 196, 77-83, 2002.10.1051/jbio/2002196010077]Search in Google Scholar
[Linnman C, Borsook D. Completing the Pain Circuit: Recent Advances in Imaging Pain and Inflammation beyond the Central Nervous System. Rambam Maimonides Med J 4, e0026, 2013.10.5041/RMMJ.10133]Search in Google Scholar
[Lonstein JS, Stern JM. Somatosensory contributions to c-fos activation within the caudal periaqueductal gray of lactating rats: effects of perioral, rooting, and suckling stimuli from pups. Horm Behav 32, 155-166, 1997.10.1006/hbeh.1997.1416]Open DOISearch in Google Scholar
[Lonstein JS, Stern JM. Site and behavioral specificity of periaqueductal gray lesions on postpartum sexual, maternal, and aggressive behaviors in rats. Brain Res 804, 21-35, 1998.10.1016/S0006-8993(98)00642-8]Search in Google Scholar
[Lonstein JS, Simmons DA, Stern JM. Functions of the caudal periaqueductal gray in lactating rats: kyphosis, lordosis, maternal aggression, and fearfulness. Behav Neurosci 112, 1502-1518, 1998.10.1037/0735-7044.112.6.1502]Search in Google Scholar
[Loyd DR, Murphy AZ. The role of the periaqueductal gray in the modulation of pain in males and females: are the anatomy and physiology really that different? Neural Plast 2009, 462879, 2009.10.1155/2009/462879263344919197373]Search in Google Scholar
[Maddock RJ, Garrett AS, Buonocore MH. Posterior cingulate cortex activation by emotional words: fMRI evidence from a valence decision task. Hum Brain Mapp 18, 30-41, 2003.10.1002/hbm.10075]Search in Google Scholar
[Martinez RC, de Oliveira AR, Brandao ML. Conditioned and unconditioned fear organized in the periaqueductal gray are differentially sensitive to injections of muscimol into amygdaloid nuclei. Neurobiol Learn Mem 85, 58-65, 2006.10.1016/j.nlm.2005.08.007]Open DOISearch in Google Scholar
[Mauss IB, Robinson MD. Measures of emotion: A review. Cogn Emot 23, 209-237, 2009.10.1080/02699930802204677]Open DOISearch in Google Scholar
[McNaughton N. Biology and Emotion (Problems in the Behavioural Sciences). Cambridge, Cambridge University Press, 1989.]Search in Google Scholar
[Menant O, Andersson F, Zelena D, Chaillou E. The benefits of magnetic resonance imaging methods to extend the knowledge of the anatomical organisation of the periaqueductal gray in mammals. J Chem Neuroanat 77, 110-120, 2016a.10.1016/j.jchemneu.2016.06.003]Search in Google Scholar
[Menant O, Destrez A, Deiss V, Boissy A, Delagrange P, Calandreau L, Chaillou E. Regulation des emotions chez l’animal d’elevage : focus sur les acteurs neurobiologiques. INRA Prod Anim 29, 241-254, 2016b.10.20870/productions-animales.2016.29.4.2966]Search in Google Scholar
[Menant O, Prima MC, Morisse M, Cornilleau F, Moussu C, Gautier A, Blanchon H, Meurisse M, Delagrange P, Tillet Y, Chaillou E. First evidence of neuronal connections between specific parts of the periaqueductal gray (PAG) and the rest of the brain in sheep: placing the sheep PAG in the circuit of emotion. Brain Struct Funct 223, 3297-3316, 2018.10.1007/s00429-018-1689-y]Search in Google Scholar
[Mobbs D, Petrovic P, Marchant JL, Hassabis D, Weiskopf N, Seymour B, Dolan RJ, Frith CD. When fear is near: threat imminence elicits prefrontal-periaqueductal gray shifts in humans. Science 317, 1079-1083, 2007.10.1126/science.1144298]Search in Google Scholar
[Mobbs D, Yu R, Rowe JB, Eich H, FeldmanHall O, Dalgleish T. Neural activity associated with monitoring the oscillating threat value of a tarantula. Proc Natl Acad Sci U S A 107, 20582-20586, 2010.10.1073/pnas.1009076107]Search in Google Scholar
[Monassi CR, Leite-Panissi CR, Menescal-de-Oliveira L. Ventrolateral periaqueductal gray matter and the control of tonic immobility. Brain Res Bull 50, 201-218, 1999.10.1016/S0361-9230(99)00192-6]Open DOISearch in Google Scholar
[Monteillet-Agius G, Fein J, Anton B, Evans CJ. ORL-1 and mu opioid receptor antisera label different fibers in areas involved in pain processing. J Comp Neurol 399, 373-383, 1998.10.1002/(SICI)1096-9861(19980928)399:3<373::AID-CNE6>3.0.CO;2-Y]Search in Google Scholar
[Morgan MM, Whitney PK, Gold MS. Immobility and flight associated with antinociception produced by activation of the ventral and lateral/dorsal regions of the rat periaqueductal gray. Brain Res 804, 159-166, 1998.10.1016/S0006-8993(98)00669-6]Search in Google Scholar
[Morgan MM, Carrive P. Activation of the ventrolateral periaqueductal gray reduces locomotion but not mean arterial pressure in awake, freely moving rats. Neuroscience 102, 905-910, 2001.10.1016/S0306-4522(00)00513-311182252]Open DOISearch in Google Scholar
[Moskowitz AS, Goodman RR. Autoradiographic analysis of mu1, mu2, and delta opioid binding in the central nervous system of C57BL/6BY and CXBK (opioid receptor-deficient) mice. Brain Res 360, 108-116, 1985.10.1016/0006-8993(85)91226-0]Search in Google Scholar
[Motta SC, Carobrez AP, Canteras NS. The periaqueductal gray and primal emotional processing critical to influence complex defensive responses, fear learning and reward seeking. Neurosci Biobehav Rev 76, 39-47, 2017.10.1016/j.neubiorev.2016.10.01228434586]Search in Google Scholar
[Moura LM, Canteras NS, Sukikara MH, Felicio LF. Morphine infusions into the rostrolateral periaqueductal gray affect maternal behaviors. Braz J Med Biol Res 43, 899-905, 2010.10.1590/S0100-879X20100075000852080297720802977]Open DOISearch in Google Scholar
[Najafi M, Kinnison J, Pessoa L. Dynamics of Intersubject Brain Networks during Anxious Anticipation. Front Hum Neurosci 11, 552, 2017.10.3389/fnhum.2017.00552570247929209184]Search in Google Scholar
[Nakamura T, Tomida M, Yamamoto T, Ando H, Takamata T, Kondo E, Kurasawa I, Asanuma N. The endogenous opioids related with antinociceptive effects induced by electrical stimulation into the amygdala. Open Dent J 7, 27-35, 2013.10.2174/1874210601307010027360694923539535]Search in Google Scholar
[Nashold BS Jr., Slaughter DG. Effects of stimulating or destroying the deep cerebellar regions in man. J Neurosurg 31, 172-186, 1969.10.3171/jns.1969.31.2.017248961304896130]Open DOISearch in Google Scholar
[Noriuchi MY, Kikuchi Y, Senoo A. The functional neuroanatomy of maternal love: mother’s response to infant’s attachment behaviors. Biol Psychiatry 63, 415-423, 2008.10.1016/j.biopsych.2007.05.01817686467]Open DOISearch in Google Scholar
[Nunes-de-Souza V, Nunes-de-Souza R, Rodgers RJ, Canto-de-Souza A. Blockade of 5-HT(2) receptors in the periaqueductal grey matter (PAG) abolishes the anxiolytic-like effect of 5-HT(1A) receptor antagonism in the median raphe nucleus in mice. Behav Brain Res 225, 547-553, 2011.10.1016/j.bbr.2011.07.05621839779]Search in Google Scholar
[O’Connell LA, Hofmann HA. The vertebrate mesolimbic reward system and social behavior network: a comparative synthesis. J Comp Neurol 519, 3599-5639, 2011.10.1002/cne.22735]Search in Google Scholar
[Oka T, Tsumori T, Yokota S, Yasui Y. Neuroanatomical and neurochemical organization of projections from the central amygdaloid nucleus to the nucleus retroambiguus via the periaqueductal gray in the rat. Neurosci Res 62, 286-298, 2008.1894815010.1016/j.neures.2008.10.004]Search in Google Scholar
[Osorio-Garcia MI, Croitor Sava AR, Sima DM, Nielsen FU, Himmelreich U, Van Huffel S. Quantification Improvements of 1H MRS Signals. In: Magnetic Resonance Spectroscopy (Ed. Dong-Hyun Kim), pp. 3-28, IntechOpen, London, 2012.]Search in Google Scholar
[Paradiso S, Johnson DL, Andreasen NC, O’Leary DS, Watkins GL, Ponto LL, Hichwa RD. Cerebral blood flow changes associated with attribution of emotional valence to pleasant, unpleasant, and neutral visual stimuli in a PET study of normal subjects. Am J Psychiatry 156, 1618-1629, 1999.10.1176/ajp.156.10.1618]Search in Google Scholar
[Parsons CE, Young KS, Stein A, Kringelbach ML. Intuitive parenting: understanding the neural mechanisms of parents’ adaptive responses to infants. Curr Opin Psychol 15, 40-44, 2017.10.1016/j.copsyc.2017.02.010]Search in Google Scholar
[Pereira EA, Lu G, Wang S, Schweder PM, Hyam JA, Stein JF, Paterson DJ, Aziz TZ, Green AL. Ventral periaqueductal grey stimulation alters heart rate variability in humans with chronic pain. Exp Neurol 223, 574-581, 2010.10.1016/j.expneurol.2010.02.004]Search in Google Scholar
[Pesini P, Pego-Reigosa R, Tramu G, Covenas R. Distribution of alpha-neoendorphin immunoreactivity in the diencephalon and the brainstem of the dog. J Chem Neuroanat 22, 251-262, 2001.10.1016/S0891-0618(01)00136-311719022]Open DOISearch in Google Scholar
[Phelps EA, LeDoux JE. Contributions of the amygdala to emotion processing: from animal models to human behavior. Neuron 48, 175-187, 2005.10.1016/j.neuron.2005.09.02516242399]Open DOISearch in Google Scholar
[Price DD. Central neural mechanisms that interrelate sensory and affective dimensions of pain. Mol Interv 2, 392- 403, 339, 2002.1499341510.1124/mi.2.6.39214993415]Search in Google Scholar
[Randall WL. The behavior of cats (Felis catus L.) with lesions in the caudal midbrain region. Behaviour 23, 107-134, 1964.10.1163/156853964X00102]Open DOISearch in Google Scholar
[Rea K, Roche M, Finn DP. Modulation of conditioned fear, fear-conditioned analgesia, and brain regional c-Fos expression following administration of muscimol into the rat basolateral amygdala. J Pain 12, 712-721, 2011.10.1016/j.jpain.2010.12.01021459678]Open DOISearch in Google Scholar
[Reynolds WJ, Scott B. Empathy: a crucial component of the helping relationship. J Psychiatr Ment Health Nurs 6, 363-370, 1999.10.1046/j.1365-2850.1999.00228.x]Search in Google Scholar
[Rizvi TA, Ennis M, Behbehani MM, Shipley MT. Connections between the central nucleus of the amygdala and the midbrain periaqueductal gray: topography and reciprocity. J Comp Neurol 303, 121-131, 1991.10.1002/cne.903030111]Search in Google Scholar
[Roeling TA, Veening JG, Peters JP, Vermelis ME, Nieuwenhuys R. Efferent connections of the hypothalamic “grooming area” in the rat. Neuroscience 56, 199-225, 1993.10.1016/0306-4522(93)90574-Y]Open DOISearch in Google Scholar
[Roxo MR, Franceschini PR, Zubaran C, Kleber FD, Sander JW. The limbic system conception and its historical evolution. ScientificWorldJournal 11, 2428-2441, 2011.2219467310.1100/2011/157150]Search in Google Scholar
[Roy M, Shohamy D, Daw N, Jepma M, Wimmer GE, Wager TD. Representation of aversive prediction errors in the human periaqueductal gray. Nat Neurosci 17, 1607-1612, 2014.2528261410.1038/nn.3832]Search in Google Scholar
[Russell J, Mahrabian A. Evidence for a Three-Factor Theory of Emotions. J Res Pers 11, 273-294, 1977.10.1016/0092-6566(77)90037-X]Open DOISearch in Google Scholar
[Saavedra JM, Palkovits M, Brownstein MJ, Axelrod J. Serotonin distribution in the nuclei of the rat hypothalamus and preoptic region. Brain Res 77, 157-165, 1974.10.1016/0006-8993(74)90812-9]Search in Google Scholar
[Sampaio KN, Mauad H, Biancardi VC, Barros JL, Amaral FT, Schenberg LC, Vasquez EC. Cardiovascular changes following acute and chronic chemical lesions of the dorsal periaqueductal gray in conscious rats. J Auton Nerv Syst 76, 99-107, 1999.10.1016/S0165-1838(99)00015-6]Search in Google Scholar
[Satpute AB, Wager TD, Cohen-Adad J, Bianciardi M, Choi JK, Buhle JT, Wald LL, Barrett LF. Identification of discrete functional subregions of the human periaqueductal gray. Proc Natl Acad Sci U S A, 110, 17101-17106, 2013.10.1073/pnas.1306095110380104624082116]Search in Google Scholar
[Schachter S, Singer JE. Cognitive, social, and physiological determinants of emotional state. Psychol Rev 69, 379-399, 1962.10.1037/h004623414497895]Search in Google Scholar
[Schenberg LC, Brandao CA, Vasquez EC. Role of periaqueductal gray matter in hypertension in spontaneously hypertensive rats. Hypertension 26, 1125-1128, 1995.10.1161/01.HYP.26.6.1125]Open DOISearch in Google Scholar
[Sebe F, Aubin T, Boue A, Poindron P. Mother-young vocal communication and acoustic recognition promote preferential nursing in sheep. J Exp Biol 211, 3554-3562, 2008.10.1242/jeb.01605518978219]Search in Google Scholar
[Shepherd SV, Freiwald WA. Functional networks for social communication in the Macaque Monkey. Neuron 99, 413-420, e3, 2018.10.1016/j.neuron.2018.06.027644910230017395]Search in Google Scholar
[Sela VR, Biesdorf C, Ramos DH, Zangrossi H Jr, Graeff FG, Audi EA. Serotonin-1A receptors in the dorsal periaqueductal gray matter mediate the panicolytic-like effect of pindolol and paroxetine combination in the elevated T-maze. Neurosci Lett 495, 63-66, 2011.10.1016/j.neulet.2011.03.04021421022]Search in Google Scholar
[Skultety FM. The behavioral effects of destructive lesions of the periaqueductal gray matter in adult cats. J Comp Neurol 110, 337-365, 1958.10.1002/cne.90110030313664839]Search in Google Scholar
[Snider RS, Maiti A. Cerebellar contributions to the Papez circuit. J Neurosci Res 2, 133-146, 1976.10.1002/jnr.490020204950678950678]Open DOISearch in Google Scholar
[Stewart-Williams S, Podd J. The placebo effect: dissolving the expectancy versus conditioning debate. Psychol Bull 130, 324-340, 2004.10.1037/0033-2909.130.2.32414979775]Search in Google Scholar
[Stone E, Coote JH, Allard J, Lovick TA. GABAergic control of micturition within the periaqueductal grey matter of the male rat. J Physiol 589, 2065-2078, 2011.10.1113/jphysiol.2010.202614309060421486804]Search in Google Scholar
[Subramanian HH, Balnave RJ, Holstege G. The midbrain periaqueductal gray control of respiration. J Neurosci 28, 12274-12283, 2008.10.1523/JNEUROSCI.4168-08.200819020021667170619020021]Open DOISearch in Google Scholar
[Sukikara MH, Mota-Ortiz SR, Baldo MV, Felicio LF, Canteras NS. The periaqueductal gray and its potential role in maternal behavior inhibition in response to predatory threats. Behav Brain Res 209, 226-233, 2010.10.1016/j.bbr.2010.01.04820138922]Search in Google Scholar
[Swanson LW, McKellar S. The distribution of oxytocin- and neurophysin-stained fibers in the spinal cord of the rat and monkey. J Comp Neurol 188, 87-106, 1979.10.1002/cne.901880108115910]Search in Google Scholar
[Takasaki A, Hui M, Sasaki M. Is the periaqueductal gray an essential relay center for the micturition reflex pathway in the cat? Brain Res 1317, 108-115, 2010.10.1016/j.brainres.2009.12.05720044981]Search in Google Scholar
[Tasker RR. Identification of pain processing systems by electrical stimulation of the brain. Hum Neurobiol 1, 261- 272, 1982.]Search in Google Scholar
[Teodorov E, Bernardi MM, Ferrari MF, Fior-Chadi DR, Felicio LF. Plasticity of opioid receptors in the female periaqueductal gray: multiparity-induced increase in the activity of genes encoding for mu and kappa receptors and a post-translational decrease in delta receptor expression. J Mol Neurosci 43, 175-181, 2011.10.1007/s12031-010-9407-020574683]Open DOISearch in Google Scholar
[Turner EA. Cerebral control of respiration. Brain 77, 448-486, 1954.10.1093/brain/77.3.44813208881]Search in Google Scholar
[van der Graaf M. In vivo magnetic resonance spectroscopy: basic methodology and clinical applications. Eur Biophys J 39, 527-540, 2010.10.1007/s00249-009-0517-y284127519680645]Search in Google Scholar
[Veissier I, Boissy A. Stress and welfare: two complementary concepts that are intrinsically related to the animal’s point of view. Physiol Behav 92, 429-433, 2007.10.1016/j.physbeh.2006.11.00817182067]Open DOISearch in Google Scholar
[Vianna DML, Graeff FG, Landeira-Fernandez J, Brandao ML. Lesion of the ventral periaqueductal gray reduces conditioned fear but does not change freezing by stimulation of the dorsal periaqueductal gray. Learn Mem 8, 164-169, 2001.1139063610.1101/lm.3610131137311390636]Search in Google Scholar
[Vianna DM, Brandao ML. Anatomical connections of the periaqueductal gray: specific neural substrates for different kinds of fear. Braz J Med Biol Res 36, 557-566, 2003.10.1590/S0100-879X200300050000212715074]Open DOISearch in Google Scholar
[Wager TD, Rilling JK, Smith EE, Sokolik A, Casey KL, Davidson RJ, Kosslyn SM, Rose RM, Cohen JD. Placeboinduced changes in FMRI in the anticipation and experience of pain. Science 303, 1162-1167, 2004.10.1126/science.109306514976306]Search in Google Scholar
[Wager TD, van Ast VA, Hughes BL, Davidson ML, Lindquist MA, Ochsner KN. Brain mediators of cardiovascular responses to social threat, part II: Prefrontal-subcortical pathways and relationship with anxiety. Neuroimage 47, 836-851, 2009.10.1016/j.neuroimage.2009.05.044416988019465135]Open DOISearch in Google Scholar
[Walker P, Carrive P. Role of ventrolateral periaqueductal gray neurons in the behavioral and cardiovascular responses to contextual conditioned fear and poststress recovery. Neuroscience 116, 897-912, 2003.10.1016/S0306-4522(02)00744-3]Search in Google Scholar
[Wiedenmayer CP, Barr GA. Mu opioid receptors in the ventrolateral periaqueductal gray mediate stress-induced analgesia but not immobility in rat pups. Behav Neurosci 114, 125-136, 2000.10.1037/0735-7044.114.1.125]Search in Google Scholar
[Wu D, Wang S, Stein JF, Aziz TZ, Green AL. Reciprocal interactions between the human thalamus and periaqueductal gray may be important for pain perception. Exp Brain Res 232, 527-534, 2014.10.1007/s00221-013-3761-4]Search in Google Scholar
[Xavier CH, Ianzer D, Lima AM, Marins FR, Pedrino GR, Vaz G, Menezes GB, Nalivaiko E, Fontes MA. Excitatory amino acid receptors mediate asymmetry and lateralization in the descending cardiovascular pathways from the dorsomedial hypothalamus. PLoS One 9, e112412, 2014.2539788410.1371/journal.pone.0112412]Search in Google Scholar
[Yoshida W, Seymour B, Koltzenburg M, Dolan RJ. Uncertainty increases pain: evidence for a novel mechanism of pain modulation involving the periaqueductal gray. J Neurosci 33, 5638-5646, 2013.2353607810.1523/JNEUROSCI.4984-12.2013]Search in Google Scholar
[Yoshimura R, Kiyama H, Kimura T, Araki T, Maeno H, Tanizawa O, Tohyama M. Localization of oxytocin receptor messenger ribonucleic acid in the rat brain. Endocrinology 133, 1239-1246, 1993.10.1210/endo.133.3.8396014]Search in Google Scholar
[Young RF, Kroening R, Fulton W, Feldman RA, Chambi I. Electrical stimulation of the brain in treatment of chronic pain. Experience over 5 years. J Neurosurg 62, 389-396, 1985.10.3171/jns.1985.62.3.0389]Search in Google Scholar
[Young KS, Parsons CE, Stein A, Vuust P, Craske MG, Kringelbach ML. The neural basis of responsive caregiving behaviour: Investigating temporal dynamics within the parental brain. Behav Brain Res 325, 105-116, 2017.10.1016/j.bbr.2016.09.012]Search in Google Scholar
[Yu CX, Li B, Xu YK, Ji TT, Li L, Zhao CJ, Chen L, Zhuo ZZ. Altered functional connectivity of the periaqueductal gray in chronic neck and shoulder pain. Neuroreport 28, 720-725, 2017.2857492710.1097/WNR.0000000000000819]Search in Google Scholar
[Zhang SP, Bandler R, Carrive P. Flight and immobility evoked by excitatory amino acid microinjection within distinct parts of the subtentorial midbrain periaqueductal gray of the cat. Brain Res 520, 73-82, 1990.10.1016/0006-8993(90)91692-A]Search in Google Scholar