scholarly journals Nociceptive TRP Channels and Sex Steroids

2021 ◽  
Author(s):  
Óscar Enciso-Pablo ◽  
Karina Angélica Méndez-Reséndiz ◽  
Tamara Rosenbaum ◽  
Sara Luz Morales-Lázaro
Keyword(s):  
Sensory Neurons ◽  
Sex Steroids ◽  
Essential Role ◽  
Transient Receptor Potential ◽  
Trp Channels ◽  
Receptor Potential ◽  
Environmental Signals ◽  
Nonselective Cation Channels ◽  
Close Relationship ◽  
Transient Receptor

Proteins belonging to Transient Receptor Potential (TRP) family are nonselective cation channels that play an essential role in mammalian physiology, functioning as transducers of several environmental signals including those of chemical, thermal and mechanical natures. A subgroup of these receptors is expressed in sensory neurons where they are activated by noxious stimuli and are key players of pain responses in the organism. Some TRP channels are molecular targets for the classical and non-classical effects of sex steroids. This chapter will describe the close relationship between nociceptive TRP channels and sex steroids as well as their impact on nociception and pain-related responses.

scholarly journals Steroids and TRP Channels: A Close Relationship

2020 ◽  
Vol 21 (11) ◽  
pp. 3819
Author(s):  
Karina Angélica Méndez-Reséndiz ◽  
Óscar Enciso-Pablo ◽  
Ricardo González-Ramírez ◽  
Rebeca Juárez-Contreras ◽  
Tamara Rosenbaum ◽  
...  
Keyword(s):  
Transient Receptor Potential ◽  
Cell Function ◽  
Trp Channels ◽  
Protein Complexes ◽  
Transmembrane Protein ◽  
Receptor Potential ◽  
Long Term Effects ◽  
Close Relationship ◽  
Transient Receptor

Transient receptor potential (TRP) channels are remarkable transmembrane protein complexes that are essential for the physiology of the tissues in which they are expressed. They function as non-selective cation channels allowing for the signal transduction of several chemical, physical and thermal stimuli and modifying cell function. These channels play pivotal roles in the nervous and reproductive systems, kidney, pancreas, lung, bone, intestine, among others. TRP channels are finely modulated by different mechanisms: regulation of their function and/or by control of their expression or cellular/subcellular localization. These mechanisms are subject to being affected by several endogenously-produced compounds, some of which are of a lipidic nature such as steroids. Fascinatingly, steroids and TRP channels closely interplay to modulate several physiological events. Certain TRP channels are affected by the typical genomic long-term effects of steroids but others are also targets for non-genomic actions of some steroids that act as direct ligands of these receptors, as will be reviewed here.

scholarly journals Emerging Perspectives on Pain Management by Modulation of TRP Channels and ANO1

2019 ◽  
Vol 20 (14) ◽  
pp. 3411 ◽  
Author(s):  
Yasunori Takayama ◽  
Sandra Derouiche ◽  
Kenta Maruyama ◽  
Makoto Tominaga
Keyword(s):  
Sensory Neurons ◽  
Transient Receptor Potential ◽  
Trp Channels ◽  
Fungal Infections ◽  
Receptor Potential ◽  
The Body ◽  
Primary Sensory Neurons ◽  
Anoctamin 1 ◽  
Neuronal Excitation ◽  
Transient Receptor

Receptor-type ion channels are critical for detection of noxious stimuli in primary sensory neurons. Transient receptor potential (TRP) channels mediate pain sensations and promote a variety of neuronal signals that elicit secondary neural functions (such as calcitonin gene-related peptide [CGRP] secretion), which are important for physiological functions throughout the body. In this review, we focus on the involvement of TRP channels in sensing acute pain, inflammatory pain, headache, migraine, pain due to fungal infections, and osteo-inflammation. Furthermore, action potentials mediated via interactions between TRP channels and the chloride channel, anoctamin 1 (ANO1), can also generate strong pain sensations in primary sensory neurons. Thus, we also discuss mechanisms that enhance neuronal excitation and are dependent on ANO1, and consider modulation of pain sensation from the perspective of both cation and anion dynamics.

scholarly journals Olfactory memory consolidation requires the TRPV channel OSM-9 in sensory neurons of the circuit.

2020 ◽  
Author(s):  
Kelli L. Benedetti ◽  
Fatema A Saifuddin ◽  
Julia M Miller ◽  
Rashmi Chandra ◽  
Alec Chen ◽  
...  
Keyword(s):  
Sensory Neurons ◽  
Memory Consolidation ◽  
Transient Receptor Potential ◽  
Trp Channels ◽  
Receptor Potential ◽  
Olfactory Memory ◽  
Nociceptive Neurons ◽  
C Elegans ◽  
Endogenous Expression ◽  
Transient Receptor

Memory is one of the most important abilities of the brain. It is defined as an alteration in behavior as a consequence of an experience. For example, the C. elegans nematode will downregulate its chemotactic response to the innately attractive odor, butanone, if the odor is not paired with food. Through repeated, spaced training with this odor in the absence of food, C. elegans will maintain this memory for a prolonged period of time. Although transient receptor potential (TRP) channels are classically thought of as primary sensory receptors, it was reported that the OSM-9/TRPV5/TRPV6 (TRP vanilloid 5/6) channel is required for single exposure learning. Here we describe a new role for osm-9 in consolidation of memory that is induced by repeated, spaced training. In this paradigm, osm-9 mutant animals learn as well as wild-types, but are unable to consolidate the memory. Though sleep is required for memory consolidation, loss of the TRPV channel OSM-9 does not affect sleep. This indicates that the TRP channel promotes memory in a process that acts outside the sleep pathway. We investigate the endogenous expression pattern of OSM-9 and show that it is not expressed in the butanone-responsive AWC olfactory sensory neuron. Instead, it is expressed in the paired AWA olfactory neuron, the ASH nociceptive neurons, the OLQ and two other unidentified sensory neurons which are most likely ADF and ADL as they express osm-9 mRNA. Because OSM-9 acts in sensory neurons that do not participate in butanone sensation, this indicates that the circuit participates in olfactory memory consolidation.

Intragastric administration of capsiate, a transient receptor potential channel agonist, triggers thermogenic sympathetic responses

2011 ◽  
Vol 110 (3) ◽  
pp. 789-798 ◽  
Author(s):  
Kaori Ono ◽  
Masako Tsukamoto-Yasui ◽  
Yoshiko Hara-Kimura ◽  
Naohiko Inoue ◽  
Yoshihito Nogusa ◽  
...  
Keyword(s):  
Sympathetic Nerve ◽  
Transient Receptor Potential ◽  
Trp Channels ◽  
Low Frequency ◽  
Receptor Potential ◽  
Transient Receptor Potential Channel ◽  
Intragastric Administration ◽  
Brown Adipose ◽  
Reflex Arc ◽  
Transient Receptor

The sympathetic thermoregulatory system controls the magnitude of adaptive thermogenesis in correspondence with the environmental temperature or the state of energy intake and plays a key role in determining the resultant energy storage. However, the nature of the trigger initiating this reflex arc remains to be determined. Here, using capsiate, a digestion-vulnerable capsaicin analog, we examined the involvement of specific activation of transient receptor potential (TRP) channels within the gastrointestinal tract in the thermogenic sympathetic system by measuring the efferent activity of the postganglionic sympathetic nerve innervating brown adipose tissue (BAT) in anesthetized rats. Intragastric administration of capsiate resulted in a time- and dose-dependent increase in integrated BAT sympathetic nerve activity (SNA) over 180 min, which was characterized by an emergence of sporadic high-activity phases composed of low-frequency bursts. This increase in BAT SNA was abolished by blockade of TRP channels as well as of sympathetic ganglionic transmission and was inhibited by ablation of the gastrointestinal vagus nerve. The activation of SNA was delimited to BAT and did not occur in the heart or pancreas. These results point to a neural pathway enabling the selective activation of the central network regulating the BAT SNA in response to a specific stimulation of gastrointestinal TRP channels and offer important implications for understanding the dietary-dependent regulation of energy metabolism and control of obesity.

scholarly journals Functional Interaction among KCa and TRP Channels for Cardiovascular Physiology: Modern Perspectives on Aging and Chronic Disease

2019 ◽  
Vol 20 (6) ◽  
pp. 1380 ◽  
Author(s):  
Erik Behringer ◽  
Md Hakim
Keyword(s):  
Blood Flow ◽  
Transient Receptor Potential ◽  
Trp Channels ◽  
Receptor Potential ◽  
The Body ◽  
Cardiovascular Physiology ◽  
Treatment And Prevention ◽  
Kca Channels ◽  
Age Related ◽  
Transient Receptor

Effective delivery of oxygen and essential nutrients to vital organs and tissues throughout the body requires adequate blood flow supplied through resistance vessels. The intimate relationship between intracellular calcium ([Ca2+]i) and regulation of membrane potential (Vm) is indispensable for maintaining blood flow regulation. In particular, Ca2+-activated K+ (KCa) channels were ascertained as transducers of elevated [Ca2+]i signals into hyperpolarization of Vm as a pathway for decreasing vascular resistance, thereby enhancing blood flow. Recent evidence also supports the reverse role for KCa channels, in which they facilitate Ca2+ influx into the cell interior through open non-selective cation (e.g., transient receptor potential; TRP) channels in accord with robust electrical (hyperpolarization) and concentration (~20,000-fold) transmembrane gradients for Ca2+. Such an arrangement supports a feed-forward activation of Vm hyperpolarization while potentially boosting production of nitric oxide. Furthermore, in vascular types expressing TRP channels but deficient in functional KCa channels (e.g., collecting lymphatic endothelium), there are profound alterations such as downstream depolarizing ionic fluxes and the absence of dynamic hyperpolarizing events. Altogether, this review is a refined set of evidence-based perspectives focused on the role of the endothelial KCa and TRP channels throughout multiple experimental animal models and vascular types. We discuss the diverse interactions among KCa and TRP channels to integrate Ca2+, oxidative, and electrical signaling in the context of cardiovascular physiology and pathology. Building from a foundation of cellular biophysical data throughout a wide and diverse compilation of significant discoveries, a translational narrative is provided for readers toward the treatment and prevention of chronic, age-related cardiovascular disease.

Sign in / Sign up

Export Citation Format

Share Document