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Neuropeptides as neuroprotective agents: Oxytocin a forefront developmental player in the mammalian brain
Abstract
Oxytocin (OT) plays a major role in the establishment of social bonds. Social bonds are linked to the activation of cell signaling pathways that promote neurotrophic and synaptic maturation, plasticity and memory changes. Anti-social behavior is often associated with abnormalities of cell signaling pathways and/or defective function of brain neurotransmitters within behavioral CNS circuits due to unproper environmental and social factors, such as, diet, stress, chemical, air pollution, and noise, during gestational period or/and during early postnatal development. OT exerts an important regulatory functions in maternity and parental behaviors, lactation, attachment, bonding, trust, and sensorial functions such as: homeostatic cardiovascular control, satiety, touch, pain, analgesia and sexual behavior. Noteworthy, OT displays important neuroprotective properties against fetal programmed hypertension when administered during early postnatal life, added to its known anabolic properties shown in adult rats, e.g. body weight control, reduces blood pressure, and increases analgesia. This review focuses on the new evidences supporting OT's role as a major neuroprotective nonapeptide provided by its quality to reverse hypertension programmed in utero by undernutrition.
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“In addition to brain, oxytocin and oxytocin receptors are found in several peripheral organs including heart, kidney, pancreas, breast, thymus, non-pregnant uterus, bowel and testis of the rat and human (Vargas-Martínez et al., 2014).”
From Lysosomal Cathepsin A Plays a Significant Role in the Processing of Endogenous Bioactive Peptides (2016) · cites this paper as Vargas-Martínez et al., 2014
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Metadata
- Authors
- Vargas-Martínez, F., Uvnäs-Moberg, K., Petersson, M., Olausson, H. A., & Jiménez-Estrada, I.
- Venue
- Progress in Neurobiology
- Publisher
- Elsevier BV
- Published
- 2014-12
- Volume
- 123
- Pages
- 37-78
- ISSN
- 0301-0082
- Cited by
- 51
- References
- 88
- Language
- en
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