Abstract

The hypothalamic neuroendocrine system is mainly composed of the neural structures regulating hormone secretion from the pituitary gland and has been considered as the higher regulatory center of the immune system. Recently, the hypothalamo-neurohypophysial system (HNS) emerged as an important component of neuroendocrine–immune network, wherein the oxytocin (OT)-secreting system (OSS) plays an essential role. The OSS, consisting of OT neurons in the supraoptic nucleus, paraventricular nucleus, their several accessory nuclei and associated structures, can integrate neural, endocrine, metabolic, and immune information and plays a pivotal role in the development and functions of the immune system. The OSS can promote the development of thymus and bone marrow, perform immune surveillance, strengthen immune defense, and maintain immune homeostasis. Correspondingly, OT can inhibit inflammation, exert antibiotic-like effect, promote wound healing and regeneration, and suppress stress-associated immune disorders. In this process, the OSS can release OT to act on immune system directly by activating OT receptors or through modulating activities of other hypothalamic–pituitary–immune axes and autonomic nervous system indirectly. However, our understandings of the role of the OSS in neuroendocrine regulation of immune system are largely incomplete, particularly its relationship with other hypothalamic–pituitary–immune axes and the vasopressin-secreting system that coexists with the OSS in the HNS. In addition, it remains unclear about the relationship between the OSS and peripherally produced OT in immune regulation, particularly intrathymic OT that is known to elicit central immunological self-tolerance of T-cells to hypophysial hormones. In this work, we provide a brief review of current knowledge of the features of OSS regulation of the immune system and of potential approaches that mediate OSS coordination of the activities of entire neuroendocrine–immune network.

Highlights

  • Immune activities are regulated by many factors, such as the genetic individual variations, immune cytokine, hormone, emotion, nutrition, metabolism, sleep, age, neural activity, and pathogens

  • Changes in neuroendocrine activities can affect the immune response through pituitary tropic hormones and the autonomic nervous system [7]

  • The regulatory effects of OT on immune responses should allow OT to influence the progress of autoimmune diseases, which is supported by the finding that in women living with HIV, high levels of OT were positively associated with CD4+ cell counts [49]

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Summary

Approaches Mediating Oxytocin Regulation of the Immune System

Reviewed by: Honoo Satake, Suntory, Japan Salvatore Andrea Mastrolia, University of Bari, Italy Vincent Geenen, University of Liège, Belgium. OT can inhibit inflammation, exert antibiotic-like effect, promote wound healing and regeneration, and suppress stress-associated immune disorders. In this process, the OSS can release OT to act on immune system directly by activating OT receptors or through modulating activities of other hypothalamic–pituitary–immune axes and autonomic nervous system indirectly. Our understandings of the role of the OSS in neuroendocrine regulation of immune system are largely incomplete, its relationship with other hypothalamic–pituitary–immune axes and the vasopressin-secreting system that coexists with the OSS in the HNS. We provide a brief review of current knowledge of the features of OSS regulation of the immune system and of potential approaches that mediate OSS coordination of the activities of entire neuroendocrine–immune network

INTRODUCTION
Humans and animals
Myocardial cell
Diabetic rats
Immune Surveillance
Strengthening Immune Defense
Maintenance of Immune Homeostasis
Other Immune Functions
Adverse Effect
RELATIONSHIP BETWEEN THE OSS AND OTHER NEUROENDOCRINE REGULATORY SYSTEMS
Comparison of Immune Regulatory Effects of VP versus OT
Relationship between the OSS and Other Neuroendocrine Activities
Intrathymic OT versus the OSS in Immune Regulation
CONCLUSION

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