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Bidirectional Effects of Mother-Young Contact on the Maternal and Neonatal Brains

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Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 1015))

Abstract

Adaptive plasticity occurs intensely during the early postnatal period through processes like proliferation, migration, differentiation, synaptogenesis, myelination and apoptosis. Exposure to particular stimuli during this critical period has long-lasting effects on cognition, stress reactivity and behavior. Maternal care is the main source of social, sensory and chemical stimulation to the young and is, therefore, critical to “fine-tune” the offspring’s neural development. Mothers providing a low quantity or quality of stimulation produce offspring that will exhibit reduced cognitive performance, impaired social affiliation and increased agonistic behaviors. Transgenerational transmission of such traits occurs epigenetically, i.e., through mechanisms like DNA methylation and post-translational modification of nucleosomal histones, processes that silence or increase gene expression without affecting the DNA sequence. Reciprocally, providing maternal care profoundly affects the behavior, learning, memory and fine neuroanatomy of the adult female. Such effects are in many cases permanent and sometimes they involve the hormones of pregnancy and lactation. The above evidence supports the idea that the mother-young dyad exerts profound and permanent effects on the brains of both adult and developing organisms, respectively. Effects on the latter can be explained by the neural developmental processes taking place during the early postnatal period. In contrast, little is known about the mechanisms mediating the plasticity of the adult maternal brain. The bidirectional effects that mother and young exert on each other’s brains exemplify a remarkable plasticity of this organ for organizing itself and provide an immense source of variability for adaptation and evolution in mammals.

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Abbreviations

5-HIAA:

5-Hydroxyindoleacetic acid

5-HT:

5-Hydroxytryptamine

ACTH:

Adrenocorticotrophin hormone

ADP-ribosyl:

Adenosin diphosphate-ribosyl

AMG:

Amygdala

AMPA:

α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid

AR:

Artificial rearing

AVP:

Arginine vasopressin

BDNF:

Brain-derived neurotrophic factor

bFGF:

Basic Fibroblast growth factor

BNST:

Bed nucleus of the stria terminalis

CA1:

Field CA1 of hippocampus

CA3:

Field CA3 of hippocampus

CBZ:

Benzodiazepines

CeA:

Central nucleus of the amygdala

CD38:

Transmembrane glycoprotein

CNS:

Central nervous system

CORT:

Corticosterone

CREB:

cAMP response element-binding protein

CRF:

Corticotropin-releasing factor

CRF ir :

Corticotrophin-releasing factor -like immunoreactivity

CSF:

Cerebrospinal fluid

DA:

Dopamine

DNA:

Deoxyribonucleid acid

DRN:

Dorsal Raphe nucleus

EPM:

Elevated plus maze

FC:

Frontal cortex

FS:

Forced swimming test

GABA:

γ-aminobutyric acid

GAP-43:

Growth associated protein 43

GC:

Glucocorticoid

GFAP:

Glial fibrillary acidic protein

LC/PBN:

Locus coeruleus/parabrachial nucleus

LG-ABN:

Licking/grooming arched-back nursing

LH:

Luteinizing hormone

MAPK:

Mitogen-activated protein kinase

mRNA:

Ribonucleic acid messenger

MB:

Maternal behavior

MD:

Maternal deprivation

MeA:

Medial amygdale

mPFC:

Medial Prefrontal cortex

MPOA:

Medial preoptic area

MR:

Mother rearing

MS:

Maternal Separation

NAcc:

Nucleus accumbens

NCAM:

Neural cell adhesion molecule

Neu-N:

Neural structural protein

NMDA:

N-Methyl-D-aspartic acid

NTS:

Nucleus tractus solitarius

OT:

Oxytocin

PFC:

Prefrontal cortex

P:

Posnatal day

PRL:

Prolactin

PVN:

Paraventricular nucleus

S-100β:

Astrocyte marker protein

SERT:

Serotonin transporter

SHR:

Spontaneous hypertensive rats

SON:

Supraoptic nucleus

UV:

Ultrasonic vocalization

WKY:

Wistar Kyoto rat

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Acknowledgments

This work was supported by grants # 128625 and 156413 (to GGM and AIM, respectively) from CONACYT (National Council of Science and Technology, Mexico). Partial support was received from grant # 181334 to Grupo de Investigación G3, CONACYT. The authors thank Mayra Flores-Jiménez for her help in the preparation of the tables.

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Correspondence to Gabriela González-Mariscal .

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González-Mariscal, G., Melo, A.I. (2017). Bidirectional Effects of Mother-Young Contact on the Maternal and Neonatal Brains. In: von Bernhardi, R., Eugenín, J., Muller, K. (eds) The Plastic Brain. Advances in Experimental Medicine and Biology, vol 1015. Springer, Cham. https://doi.org/10.1007/978-3-319-62817-2_6

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