Intrauterine Exposure to Chronic 22 kHz Sound Affects Inhibitory Avoidance and Serotonergic Parameters in Forebrain Areas of Dams and Rat Offspring
Read full paper at:
http://www.scirp.org/journal/PaperInformation.aspx?PaperID=54047#.VOBRRSzQrzE
http://www.scirp.org/journal/PaperInformation.aspx?PaperID=54047#.VOBRRSzQrzE
Author(s)
Patrícia da Silva Oliveira1, Ariomester Nascimento Daniel1, Polliana Toledo Nunes1, Karina Abdo Costa1, Hani Camille Yehia1,2, Angela Maria Ribeiro1,3*
Affiliation(s)
1Programa
de Pós-Graduação em Neurociências, Laboratório de Neurociências
Comportamental e Molecular, LaNeC, Universidade Federal de Minas Gerais,
Belo Horizonte, Brazil.
2Departamento de Engenharia Eletrônica, Escola de Engenharia, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
3Departamento de Bioquímica e Imunologia, ICB and Departamento de Psicologia, FaFiCH, Laboratório de Neurociências Comportamental e Molecular, LaNeC, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
2Departamento de Engenharia Eletrônica, Escola de Engenharia, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
3Departamento de Bioquímica e Imunologia, ICB and Departamento de Psicologia, FaFiCH, Laboratório de Neurociências Comportamental e Molecular, LaNeC, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
ABSTRACT
In
the present study we evaluated the effects of chronic exposure to
sounds at 22 kHz during pregnancy on the central serotonergic and
behavioral parameters in Wistar rat dams after the suckling period and
on their male rat offspring. In addition, we also assessed the effects
of an acute 22 kHz sound, associated with the chronic intrauterine
exposure, on the emotional responses of adult offspring. The primary
hypothesis was that experiencing 22 kHz stimuli during an early stage of
development would interfere with brain serotonergic parameters and,
later, with the adult rat’s defensive responses. The corollary question
was whether a 22 kHz sound exposure would differentially affect
inhibitory avoidance and escape responses and central serotonergic
parameters. Female rats were divided into four groups: non-pregnant
control; non-pregnant chronic exposure; pregnant control; and pregnant
chronic exposure. Male offspring were divided into four groups: chronic
intrauterine sound exposure; acute sound exposure in adulthood; chronic
intrauterine exposure with acute exposure in adulthood; and no exposure.
Chronic sound exposure affected inhibitory avoidance and serotonergic
parameters in female rats. For offspring, there was an interaction
between chronic and acute sound exposure effects on inhibitory avoidance
response but not on escape response. There were significant effects of
chronic intrauterine exposure on serotonin turnover in the hippocampus
and PFC of females. For offspring, the turnover was increased by chronic
exposure only in PFC, and in amygdala it was increased by acute
exposure. These results illuminate the potential of an early acoustic
sound exposure for causing central serotonergic and emotional behavioral
changes that can persist into later periods of life.
KEYWORDS
Cite this paper
References
da
Silva Oliveira, P. , Daniel, A. , Nunes, P. , Costa, K. , Yehia, H. and
Ribeiro, A. (2015) Intrauterine Exposure to Chronic 22 kHz Sound
Affects Inhibitory Avoidance and Serotonergic Parameters in Forebrain
Areas of Dams and Rat Offspring. Journal of Behavioral and Brain Science, 5, 25-39. doi: 10.4236/jbbs.2015.52003.
| [1] | Anderson, J.W. (1954) The Production of Ultrasonic Sounds by Laboratory Rats and Other Mammals. Science, 119, 808-809. http://dx.doi.org/10.1126/science.119.3101.808 |
| [2] | Brudzynski,
S.M., et al. (1993) Analysis of 22 kHz Ultrasonic Vocalization in
Laboratory Rats: Long and Short Calls. Physiology & Behavior, 54,
215-221. http://dx.doi.org/10.1016/0031-9384(93)90102-L |
| [3] | Wohr,
M., Borta, A. and Schwarting, R.K. (2005) Overt Behavior and Ultrasonic
Vocalization in a Fear Conditioning Paradigm: A Dose-Response Study in
the Rat. Neurobiology of Learning and Memory, 84, 228-240. http://dx.doi.org/10.1016/j.nlm.2005.07.004 |
| [4] | Wohr,
M. and Schwarting, R.K. (2013) Affective Communication in Rodents:
Ultrasonic Vocalizations as a Tool for Research on Emotion and
Motivation. Cell and Tissue Research, 354, 81-97. http://dx.doi.org/10.1007/s00441-013-1607-9 |
| [5] | Blanchard,
R.J., et al. (1992) Sex Differences in the Incidence and Sonographic
Characteristics of Antipredator Ultrasonic Cries in the Laboratory Rat
(Rattusnorvegicus). Journal of Comparative Psychology, 106, 270-277. http://dx.doi.org/10.1037/0735-7036.106.3.270 |
| [6] | Thomas,
D.A., Takahashi, L.K. and Barfield, R.J. (1983) Analysis of Ultrasonic
Vocalizations Emitted by Intruders during Aggressive Encounters among
Rats (Rattusnorvegicus). Journal of Comparative Psychology, 97, 201-206. http://dx.doi.org/10.1037/0735-7036.97.3.201 |
| [7] | Parsana,
A.J., Li, N. and Brown, T.H. (2012) Positive and Negative Ultrasonic
Social Signals Elicit Opposing Firing Patterns in Rat Amygdala.
Behavioural Brain Research, 226, 77-86. http://dx.doi.org/10.1016/j.bbr.2011.08.040 |
| [8] | Sadananda,
M., Wohr, M. and Schwarting, R.K. (2008) Playback of 22-kHz and 50-kHz
Ultrasonic Vocalizations Induces Differential c-fos Expression in Rat
Brain. Neuroscience Letters, 435, 17-23. http://dx.doi.org/10.1016/j.neulet.2008.02.002 |
| [9] | Jelen,
P., Soltysik, S. and Zagrodzka, J. (2003) 22-kHz Ultrasonic
Vocalization in Rats as an Index of Anxiety but Not Fear: Behavioral and
Pharmacological Modulation of Affective State. Behavioural Brain
Research, 141, 63-72. http://dx.doi.org/10.1016/S0166-4328(02)00321-2 |
| [10] | Lucas, A. (1994) Role of Nutritional Programming in Determining Adult Morbidity. Archives of Disease in Childhood, 71, 288-290. http://dx.doi.org/10.1136/adc.71.4.288 |
| [11] | Whimbey,
A.E. and Denenberg, V.H. (1967) Experimental Programming of Life
Histories: The Factor Structure Underlying Experimentally Created
Individual Differences. Behaviour, 29, 296-314. http://dx.doi.org/10.1163/156853967X00163 |
| [12] | Lucas, A. (1991) Programming by Early Nutrition in Man. Ciba Foundation Symposium, 156, 38-50 (Discussion 50-55). |
| [13] | Lesage,
J., Del-Favero, F., Leonhardt, M., Louvart, H., Maccari, S., Vieau, D.
and Darnaudery, M. (2004) Prenatal Stress Induces Intrauterine Growth
Restriction and Programmes Glucose Intolerance and Feeding Behaviour
Disturbances in the Aged Rat. Journal of Endocrinology, 181, 291-296. http://dx.doi.org/10.1677/joe.0.1810291 |
| [14] | Matsumoto,
M., Yoshioka, M. and Togashi, H. (2009) Early Postnatal Stress and
Neural Circuit Underlying Emotional Regulation. International Review of
Neurobiology, 85, 95-107. http://dx.doi.org/10.1016/S0074-7742(09)85007-1 |
| [15] | Anacker, C., O’Donnell, K.J. and Meaney, M.J. (2014) Early Life Adversity and the Epigenetic Programming of Hypothalamic-Pituitary-Adrenal Function. Dialogues in Clinical Neuroscience, 16, 321-333. |
| [16] | Levine,
S. (2002) Regulation of the Hypothalamic-Pituitary-Adrenal Axis in the
Neonatal Rat: The Role of Maternal Behavior. Neurotoxicity Research, 4,
557-564. http://dx.doi.org/10.1080/10298420290030569 |
| [17] | Vazquez,
D.M., Bailey, C., Dent, G.W., Okimoto, D.K., Steffek, A., López, J.F.
and Levine, S. (2006) Brain Corticotropin-Releasing Hormone (CRH)
Circuits in the Developing Rat: Effect of Maternal Deprivation. Brain
Research, 1121, 83-94. http://dx.doi.org/10.1016/j.brainres.2006.08.104 |
| [18] | Kim,
C.H., Lee, S.-C., Shin, J.W., Chung, K.-J., Lee, S.-H., Shin, M.-S., et
al. (2013) Exposure to Music and Noise during Pregnancy Influences
Neurogenesis and Thickness in Motor and Somatosensory Cortex of Rat
Pups. International Neurourology Journal, 17, 107-113. http://dx.doi.org/10.5213/inj.2013.17.3.107 |
| [19] | Graeff, F.G., Viana, M.B. and Tomaz, C. (1993) The Elevated T Maze, a New Experimental Model of Anxiety and Memory: Effect of Diazepam. Brazilian Journal of Medical and Biological Research, 26, 67-70. |
| [20] | Pellow,
S., Chopin, P., File, S.E. and Briley, M. (1985) Validation of Open:
Closed Arm Entries in an Elevated Plus-Maze as a Measure of Anxiety in
the Rat. Journal of Neuroscience Methods, 14, 149-167. http://dx.doi.org/10.1016/0165-0270(85)90031-7 |
| [21] | Graeff,
F.G., Netto, C.F. and Zangrossi Jr., H. (1998) The Elevated T-Maze as
an Experimental Model of Anxiety. Neuroscience & Biobehavioral
Reviews, 23, 237-246. http://dx.doi.org/10.1016/S0149-7634(98)00024-4 |
| [22] | Viana,
M.B., Tomaz, C. and Graeff, F.G. (1994) The Elevated T-Maze: A New
Animal Model of Anxiety and Memory. Pharmacology Biochemistry and
Behavior, 49, 549-554. http://dx.doi.org/10.1016/0091-3057(94)90067-1 |
| [23] | Zangrossi
Jr., H. and Graeff, F.G. (1997) Behavioral Validation of the Elevated
T-Maze: A New Animal Model of Anxiety. Brain Research Bulletin, 44, 1-5.
http://dx.doi.org/10.1016/S0361-9230(96)00381-4 |
| [24] | Graeff,
F.G. (2007) Anxiety, Panic and the Hypothalamic-Pituitary-Adrenal Axis.
The Revista Brasileira de Psiquiatria, 29, S3-S6. http://dx.doi.org/10.1590/S1516-44462007000500002 |
| [25] | Graeff,
F.G., Viana, M.B. and Mora, P.O. (1996) Opposed Regulation by Dorsal
Raphe Nucleus 5-HT Pathways of Two Types of Fear in the Elevated T-Maze.
Pharmacology Biochemistry and Behavior, 53, 171-177. http://dx.doi.org/10.1016/0091-3057(95)02012-8 |
| [26] | Zangrossi Jr., H. and Graeff, F.G. (2014) Serotonin in Anxiety and Panic: Contributions of the Elevated T-Maze. Neuroscience Biobehavioral Reviews, 46, 397-406. |
| [27] | Escribano, B., Quero, I., Feijóo, M., Tasset, I., Montilla, P. and Túnez, I. (2013) Role of Noise and Music as Anxiety Modulators: Relationship with Ovarian Hormones in the Rat. Applied Animal Behaviour Science, 152, 73-82. |
| [28] | de
Freitas-Silva, D.M., de Souza Resende, L., Pereira, S.R.C., Franco,
G.C. and Ribeiro, A.M. (2010) Maternal Thiamine Restriction during
Lactation Induces Cognitive Impairments and Changes in Glutamate and
GABA Concentrations in Brain of Rat Offspring. Behavioural Brain
Research, 211, 33-40. http://dx.doi.org/10.1016/j.bbr.2010.03.002 |
| [29] | Goldman,
J.M., Murr, A.S. and Cooper, R.L. (2007) The Rodent Estrous Cycle:
Characterization of Vaginal Cytology and Its Utility in Toxicological
Studies. Birth Defects Research Part B: Developmental and Reproductive
Toxicology, 80, 84-97. http://dx.doi.org/10.1002/bdrb.20106 |
| [30] | Furtak,
S.C., Allen, T.A. and Brown, T.H. (2007) Single-Unit Firing in Rat
Perirhinal Cortex Caused by Fear Conditioning to Arbitrary and
Ecological Stimuli. Journal of Neuroscience, 27, 12277-12291. http://dx.doi.org/10.1523/JNEUROSCI.1653-07.2007 |
| [31] | Paxinos,
G., et al. (1985) Bregma, Lambda and the Interaural Midpoint in
Stereotaxic Surgery with Rats of Different Sex, Strain and Weight.
Journal of Neuroscience Methods, 13, 139-143. http://dx.doi.org/10.1016/0165-0270(85)90026-3 |
| [32] | Paul,
E.D. and Lowry, C.A. (2013) Functional Topography of Serotonergic
Systems Supports the Deakin/Graeff Hypothesis of Anxiety and Affective
Disorders. Journal of Psychopharmacology, 27, 1090-1106. http://dx.doi.org/10.1177/0269881113490328 |
| [33] | Oliveira-Silva,
I.F., Pintoa, L., Pereirab, S.R.C., Ferrazc, V.P., Barbosad, A.J.A.,
Coelho, V.A.A., et al. (2007) Age-Related Deficit in Behavioural
Extinction Is Counteracted by Long-Term Ethanol Consumption: Correlation
between 5-HIAA/5HT Ratio in Dorsal Raphe Nucleus and Cognitive
Parameters. Behavioural Brain Research, 180, 226-234. http://dx.doi.org/10.1016/j.bbr.2007.03.012 |
| [34] | Shannon,
N.J., Gunnet, J.W. and Moore, K.E. (1986) A Comparison of Biochemical
Indices of 5-Hydroxytryptaminergic Neuronal Activity Following
Electrical Stimulation of the Dorsal Raphe Nucleus. Journal of
Neurochemistry, 47, 958-965. http://dx.doi.org/10.1111/j.1471-4159.1986.tb00704.x |
| [35] | Beckett,
S.R.G., Aspley, S., Graham, M. and Marsden, C.A. (1996) Pharmacological
Manipulation of Ultrasound Induced Defense Behaviour in the Rat.
Psychopharmacology, 127, 384-390. http://dx.doi.org/10.1007/s002130050102 |
| [36] | Escribano, B., Quero, I., Feijóo, M., Tasset, I., Montilla, P. and Túnez, I. (2014) Role of Noise and Music as Anxiety Modulators: Relationship with Ovarian Hormones in the Rat. Applied Animal Behaviour Science, 152, 73-82. |
| [37] | Nishio,
H., Kasuga, S., Ushijima, M. and Harada, Y. (2001) Prenatal Stress and
Postnatal Development of Neonatal Rats—Sex-Dependent Effects on
Emotional Behavior and Learning Ability of Neonatal Rats. International
Journal of Developmental Neuroscience, 19, 37-45. http://dx.doi.org/10.1016/S0736-5748(00)00070-8 |
| [38] | Naqvi,
F., Haider, S., Perveen, T. and Haleem, D.J. (2012) Sub-Chronic
Exposure to Noise Affects Locomotor Activity and Produces Anxiogenic and
Depressive like Behavior in Rats. Pharmacological Reports, 64, 64-69. http://dx.doi.org/10.1016/S1734-1140(12)70731-4 |
| [39] | Uran, S.L., Caceres, L.G. and Guelman, L.R. (2010) Effects of Loud Noise on Hippocampal and Cerebellar-Related Behaviors. Brain Research, 1361, 102-114. http://dx.doi.org/10.1016/j.brainres.2010.09.022 |
| [40] | Morozova,
A.Y., Zubkov, E.A., Storozheva, Z.I., Kekelidze, Z.I. and Chekhonin,
V.P. (2013) Effect of Ultrasonic Irradiation on the Development of
Symptoms of Depression and Anxiety in Rats. Bulletin of Experimental
Biology and Medicine, 154, 740-743. http://dx.doi.org/10.1007/s10517-013-2044-1 |
| [41] | Grissom,
N. and Bhatnagar, S. (2009) Habituation to Repeated Stress: Get Used to
It. Neurobiology of Learning and Memory, 92, 215-224. http://dx.doi.org/10.1016/j.nlm.2008.07.001 |
| [42] | Masini,
C.V., Babb, J.A., Nyhuis, T.J., Day, H.E.W. and Campeau, S. (2012)
Auditory Cortex Lesions Do Not Disrupt Habituation of HPA Axis Responses
to Repeated Noise Stress. Brain Research, 1443, 18-26. http://dx.doi.org/10.1016/j.brainres.2012.01.002 |
| [43] | Wallenius,
M.A. (2004) The Interaction of Noise Stress and Personal Project Stress
on Subjective Health. Journal of Environmental Psychology, 24, 167-177.
http://dx.doi.org/10.1016/j.jenvp.2003.12.002 |
| [44] | Abrams, R., Gerhardt, K. and Antonelli, P. (1998) Fetal Hearing. Developmental Psychobiology, 33, 1-3. http://dx.doi.org/10.1002/(SICI)1098-2302(199807)33:1<1::AID-DEV1>3.0.CO;2-P |
| [45] | Antonelli,
P.J., Gerhardt, K., Abrams, R. and Huang, X. (2002) Fetal Central
Auditory System Metabolic Response to Cochlear Implant Stimulation.
Otolaryngology—Head and Neck Surgery, 127, 131-137. http://dx.doi.org/10.1067/mhn.2002.126899 |
| [46] | Hepper, P.G. and Shahidullah, B.S. (1994) Development of Fetal Hearing. Archives of Disease in Childhood, 71, F81-F87. http://dx.doi.org/10.1136/fn.71.2.F81 |
| [47] | Geal-Dor,
M., Freeman, S., Li, G. and Sohmer, H. (1993) Development of Hearing in
Neonatal Rats: Air and Bone Conducted ABR Thresholds. Hearing Research,
69, 236-242. http://dx.doi.org/10.1016/0378-5955(93)90113-F |
| [48] | Saliu, A. (2011) The Development of Hearing in Rats: Reliability of Wave 1 as a Determinant of Auditory Maturation and Contributions of Peripheral Structure Progression. City College of New York, New York, 33. |
| [49] | Barnett,
S.B., Rott, H.-D., ter Haar, G.R., Ziskin, M.C. and Maeda, K. (1997)
The Sensitivity of Biological Tissue to Ultrasound. Ultrasound in
Medicine & Biology, 23, 805-812. http://dx.doi.org/10.1016/S0301-5629(97)00027-6 |
| [50] | Weinstock,
M. (1997) Does Prenatal Stress Impair Coping and Regulation of
Hypothalamic-Pituitary-Adrenal Axis? Neuroscience & Biobehavioral
Reviews, 21, 1-10. http://dx.doi.org/10.1016/S0149-7634(96)00014-0 |
| [51] | Weinstock,
M. (2008) The Long-Term Behavioural Consequences of Prenatal Stress.
Neuroscience & Biobehavioral Reviews, 32, 1073-1086. http://dx.doi.org/10.1016/j.neubiorev.2008.03.002 |
| [52] | Hu,
L., Yang, J., Song, T.S., Hou, N., Liu, Y., Zhao, X.G., et al. (2014) A
New Stress Model, a Scream Sound, Alters Learning and Monoamine Levels
in Rat Brain. Physiology & Behavior, 123, 105-113. http://dx.doi.org/10.1016/j.physbeh.2013.09.010 |
| [53] | Lanfumey,
L., Mongeau, R., Cohen-Salmon, C. and Hamon, M. (2008)
Corticosteroid-Serotonin Interactions in the Neurobiological Mechanisms
of Stress-Related Disorders. Neuroscience & Biobehavioral Reviews,
32, 1174-1184. http://dx.doi.org/10.1016/j.neubiorev.2008.04.006 |
| [54] | Graeff,
F.G., Garcia-Leal, C., Del-Ben, C.M. and Guimaraes, F.S. (2005) Does
the Panic Attack Activate the Hypothalamic-Pituitary-Adrenal Axis? Anais
da Academia Brasileira de Ciências, 77, 477-491. http://dx.doi.org/10.1590/S0001-37652005000300009 |
| [55] | Graeff, F.G. (2011) Defense-Related Emotions in Humans. Psychology and Neuroscience, 4, 183-189. http://dx.doi.org/10.3922/j.psns.2011.2.003 |
| [56] | Graeff,
F.G. and Zangrossi Jr., H. (2010) The Dual Role of Serotonin in Defense
and the Mode of Action of Antidepressants on Generalized Anxiety and
Panic Disorders. Central Nervous System Agents in Medicinal Chemistry,
10, 207-217. http://dx.doi.org/10.2174/1871524911006030207 |
| [57] | Graeff, F.G. (2003) Serotonin, Periaqueductal Gray Matter and Panic Disorder. Revista Brasileira de Psiquiatria, 25, 42-45. http://dx.doi.org/10.1590/S1516-44462003000600010 |
| [58] | Sanchez, C., Gruca, P. and Papp, M. (2003) R-Citalopram Counteracts the Antidepressant-Like Effect of Escitalopram in a Rat Chronic Mild Stress Model. Behavioural Pharmacology, 14, 465-470. |
| [59] | Curran, K.P. and Chalasani, S.H. (2012) Serotonin Circuits and Anxiety: What Can Invertebrates Teach Us? Invertebrate Neuroscience, 12, 81-92. |
| [60] | Maron,
E., Nutt, D. and Shlik, J. (2012) Neuroimaging of Serotonin System in
Anxiety Disorders. Current Pharmaceutical Design, 18, 5699-5708. http://dx.doi.org/10.2174/138161212803530844 |
| [61] | Graeff, F.G. (2002) On Serotonin and Experimental Anxiety. Psychopharmacology, 163, 467-476. http://dx.doi.org/10.1007/s00213-002-1112-4 |
| [62] | Rex,
A., Voigt, J.P. and Fink, H. (2005) Anxiety but Not Arousal Increases
5-Hydroxytryptamine Release in the Rat Ventral Hippocampus in Vivo.
European Journal of Neuroscience, 22, 1185-1189. http://dx.doi.org/10.1111/j.1460-9568.2005.04251.x |
| [63] | Midzyanovskaya,
I.S., Kuznetsova, G.D., van Luijtelaar, E.L.J.M., van Rijn, C.M.,
Tuomisto, L. and MacDonald, E. (2006) The Brain 5HTergic Response to an
Acute Sound Stress in Rats with Generalized (Absence and Audiogenic)
Epilepsy. Brain Research Bulletin, 69, 631-638. http://dx.doi.org/10.1016/j.brainresbull.2006.03.008 |
| [64] | Compan, V. (2007) Do Limits of Neuronal Plasticity Represent an Opportunity for Mental Diseases, Such as Addiction to Food and Illegal Drugs? Use and Utilities of Serotonin Receptor Knock-Out Mice. In: Chattopadhyay, A., Ed., Serotonin Receptors in Neurobiology, CRC Press, Boca Raton. |
| [65] | LeDoux, J. (2007) The Amygdala. Current Biology, 17, R868-R874. http://dx.doi.org/10.1016/j.cub.2007.08.005 |
| [66] | Berretta, S. (2005) Cortico-Amygdala Circuits: Role in the Conditioned Stress Response. Stress, 8, 221-232. http://dx.doi.org/10.1080/10253890500489395 |
| [67] | Shin,
L.M. and Liberzon, I. (2010) The Neurocircuitry of Fear, Stress, and
Anxiety Disorders. Neuropsychopharmacology, 35, 169-191. http://dx.doi.org/10.1038/npp.2009.83 |
| [68] | van
Marle, H.J.F., Hermans, E.J., Qin, S.Z. and Fernández, G. (2009) From
Specificity to Sensitivity: How Acute Stress Affects Amygdala Processing
of Biologically Salient Stimuli. Biological Psychiatry, 66, 649-655. http://dx.doi.org/10.1016/j.biopsych.2009.05.014 |
| [69] | Leuner, B. and Shors, T.J. (2012) Stress, Anxiety, and Dendritic Spines: What Are the Connections? Neuroscience, 251, 108-119. http://dx.doi.org/10.1016/j.neuroscience.2012.04.021 |
| [70] | Mahan,
A.L. and Ressler, K.J. (2012) Fear Conditioning, Synaptic Plasticity
and the Amygdala: Implications for Posttraumatic Stress Disorder. Trends
in Neurosciences, 35, 24-35. http://dx.doi.org/10.1016/j.tins.2011.06.007 |
| [71] | McEwen,
B.S., Eiland, L., Hunter, R.G. and Miller, M.M. (2012) Stress and
Anxiety: Structural Plasticity and Epigenetic Regulation as a
Consequence of Stress. Neuropharmacology, 62, 3-12. http://dx.doi.org/10.1016/j.neuropharm.2011.07.014 |
| [72] | Mitra,
R., Jadhav, S., McEwen, B.S., Vyas, A. and Chattarji, S. (2005) Stress
Duration Modulates the Spatiotemporal Patterns of Spine Formation in the
Basolateral Amygdala. Proceedings of the National Academy of Sciences
of the United States of America, 102, 9371-9376. http://dx.doi.org/10.1073/pnas.0504011102 |
| [73] | Mitra, R., Ferguson, D. and Sapolsky, R.M. (2009) SK2 Potassium Channel Overexpression in Basolateral Amygdala Reduces Anxiety, Stress-Induced Corticosterone Secretion and Dendritic Arborization. Molecular Psychiatry, 14, 847-855. |
| [74] | Roozendaal,
B., McReynolds, J.R., Van der Zee, E.A., Lee, S., McGaugh, J.L. and
McIntyre, C.K. (2009) Glucocorticoid Effects on Memory Consolidation
Depend on Functional Interactions between the Medial Prefrontal Cortex
and Basolateral Amygdala. Journal of Neuroscience, 29, 14299-14308. http://dx.doi.org/10.1523/JNEUROSCI.3626-09.2009 |
| [75] | Vyas,
A., Jadhav, S. and Chattarji, S. (2006) Prolonged Behavioral Stress
Enhances Synaptic Connectivity in the Basolateral Amygdala.
Neuroscience, 143, 387-393. http://dx.doi.org/10.1016/j.neuroscience.2006.08.003 eww150215lx |
评论
发表评论