Rapid signaling of steroid hormones in the vertebrate nervous system

10.2741/3970 ◽  
2012 ◽  
Vol 17 (1) ◽  
pp. 996 ◽  
Author(s):  
Hirotaka Sakamoto
Keyword(s):  
Nervous System ◽  
Steroid Hormones ◽  
Rapid Signaling

Receptor and Enzyme Mechanisms as Targets for Endocrine Disruptors

2017 ◽  
Author(s):  
Heather B. Patisaul ◽  
Scott M. Belcher
Keyword(s):  
Nervous System ◽  
Steroid Hormones ◽  
Endocrine Disruptors ◽  
Endocrine Disruption ◽  
Hormone Receptors ◽  
Mammalian Brain ◽  
Mechanistic Studies ◽  
Rapid Signaling ◽  
The Impact ◽  
The Brain

In this chapter, the current understanding of the mechanisms of endocrine disruption on the brain and nervous system are presented. Because the overwhelming majority of mechanistic studies on EDCs have focused on the actions mediated by nuclear hormone receptors, this mechanisms is described in detail. The chapter also discusses the classic transcriptional mechanisms of steroid action and the impact of EDCs on rapid signaling (non-genomic) mechanisms. It presents an overview of the enzymes and pathways involved in the biosynthesis of steroid hormones, which are critical to proper functioning of the HPA and HPG axis, and the neuroactive steroids synthesized and active in the mammalian brain. The potential for EDCs to alter metabolic enzymes, with a focus on possible targets in the metabolic blood-brain barrier, is presented as a potential, though largely unexplored, mode of EDC action in the brain.

The dare gene: steroid hormone production, olfactory behavior, and neural degeneration in Drosophila

Development ◽  
1999 ◽  
Vol 126 (20) ◽  
pp. 4591-4602 ◽  
Author(s):  
M.R. Freeman ◽  
A. Dobritsa ◽  
P. Gaines ◽  
W.A. Segraves ◽  
J.R. Carlson
Keyword(s):  
Nervous System ◽  
Steroid Hormones ◽  
Steroid Hormone ◽  
Larval Instar ◽  
Hormone Production ◽  
Ring Gland ◽  
Olfactory Stimuli ◽  
Steroid Hormone Signaling ◽  
Adrenodoxin Reductase ◽  
Strength Result

Steroid hormones mediate a wide variety of developmental and physiological events in insects, yet little is known about the genetics of insect steroid hormone biosynthesis. Here we describe the Drosophila dare gene, which encodes adrenodoxin reductase (AR). In mammals, AR plays a key role in the synthesis of all steroid hormones. Null mutants of dare undergo developmental arrest during the second larval instar or at the second larval molt, and dare mutants of intermediate severity are delayed in pupariation. These defects are rescued to a high degree by feeding mutant larvae the insect steroid hormone 20-hydroxyecdysone. These data, together with the abundant expression of dare in the two principal steroid biosynthetic tissues, the ring gland and the ovary, argue strongly for a role of dare in steroid hormone production. dare is the first Drosophila gene shown to encode a defined component of the steroid hormone biosynthetic cascade and therefore provides a new tool for the analysis of steroid hormone function. We have explored its role in the adult nervous system and found two striking phenotypes not previously described in mutants affected in steroid hormone signaling. First, we show that mild reductions of dare expression cause abnormal behavioral responses to olfactory stimuli, indicating a requirement for dare in sensory behavior. Then we show that dare mutations of intermediate strength result in rapid, widespread degeneration of the adult nervous system.

Behavioral Endocrinology: Integrating Mind and Body

2020 ◽  
Vol 4 (2) ◽  
pp. 97-110
Author(s):  
Peter T. Ellison
Keyword(s):  
Nervous System ◽  
Steroid Hormones ◽  
Behavioral Ecology ◽  
Endocrine System ◽  
Behavioral Endocrinology ◽  
Paternal Behavior ◽  
Mind And Body ◽  
The Central Nervous System ◽  
Primary Focus

Abstract The nervous system and the endocrine system interact to integrate behavior and physiology. Hormones play an important role in this interaction, particularly steroid hormones. Other molecules, notably oxytocin, can serve both as hormones in the soma and neuromodulators in the central nervous system. Understanding the influence of the endocrine system on human behavior, both individual and social, has been a primary focus of behavioral endocrinology for many decades, though technical and methodological challenges have been formidable. The recent enthusiasm for enzyme-linked immunoassay kits for measuring steroid hormones in saliva has been found to be largely unsound, for example. Despite these difficulties, advances in many areas have been made and new areas, such as the endocrinology of paternal behavior and the role of oxytocin in social interactions, have emerged. Reproductive ecology provides a theoretical framework for integrating the diverse content of human behavioral ecology.

Effects of steroid hormones on gene expression of glial markers in the central and peripheral nervous system: variations induced by aging

1998 ◽  
Vol 33 (7-8) ◽  
pp. 827-836 ◽  
Author(s):  
RobertoCosimo Melcangi ◽  
Valerio Magnaghi ◽  
Ilaria Cavarretta ◽  
MarcoAndrea Riva ◽  
Flavio Piva ◽  
...  
Keyword(s):  
Gene Expression ◽  
Nervous System ◽  
Steroid Hormones ◽  
Peripheral Nervous System

scholarly journals Steroid hormones and neurosteroids in normal and pathological aging of the nervous system

2003 ◽  
Vol 71 (1) ◽  
pp. 3-29 ◽  
Author(s):  
M. Schumacher ◽  
S. Weill-Engerer ◽  
P. Liere ◽  
F. Robert ◽  
R.J.M. Franklin ◽  
...  
Keyword(s):  
Nervous System ◽  
Steroid Hormones ◽  
Pathological Aging

scholarly journals Protective Actions of 17β-Estradiol and Progesterone on Oxidative Neuronal Injury Induced by Organometallic Compounds

2015 ◽  
Vol 2015 ◽  
pp. 1-16 ◽  
Author(s):  
Yasuhiro Ishihara ◽  
Takuya Takemoto ◽  
Atsuhiko Ishida ◽  
Takeshi Yamazaki
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Steroid Hormones ◽  
Endocrine System ◽  
Organometallic Compounds ◽  
Neuronal Injury ◽  
Neuroactive Steroids ◽  
The Central Nervous System ◽  
Neuroprotective Actions ◽  
Pass Through

Steroid hormones synthesized in and secreted from peripheral endocrine glands pass through the blood-brain barrier and play a role in the central nervous system. In addition, the brain possesses an inherent endocrine system and synthesizes steroid hormones known as neurosteroids. Increasing evidence shows that neuroactive steroids protect the central nervous system from various harmful stimuli. Reports show that the neuroprotective actions of steroid hormones attenuate oxidative stress. In this review, we summarize the antioxidative effects of neuroactive steroids, especially 17β-estradiol and progesterone, on neuronal injury in the central nervous system under various pathological conditions, and then describe our recent findings concerning the neuroprotective actions of 17β-estradiol and progesterone on oxidative neuronal injury induced by organometallic compounds, tributyltin, and methylmercury.

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