The capsaicin receptor TRPV1 has been widely characterized in the sensory system as a key component of pain and inflammation. A large amount of evidence shows that TRPV1 is also functional in the brain although its role is still debated. Here we report that TRPV1 is highly expressed in microglial cells rather than neurons of the anterior cingulate cortex and other brain areas. We found that stimulation of microglial TRPV1 controls cortical microglia activation per se and indirectly enhances glutamatergic transmission in neurons by promoting extracellular microglial microvesicles shedding. Conversely, in the cortex of mice suffering from neuropathic pain, TRPV1 is also present in neurons affecting their intrinsic electrical properties and sy...
The transient receptor potential subfamily V member 1 (TRPV1) belongs to the diverse transient recep...
Transient receptor potential cation channel, subfamily V, member 1 (TRPV1, also known as vanilloid r...
Neuropathic pain and allodynia may arise from sensitization of central circuits. We report a mechani...
The capsaicin receptor TRPV1 has been widely characterized in the sensory system as a key component ...
During neuropathic pain, caspases are activated in the limbic cortex. We investigated the role of TR...
During neuropathic pain, caspases are activated in the limbic cortex. We investigated the role of TR...
Although activation of spinal glia has been implicated in the development of pathological pain, the ...
TRPV1 is an ion channel activated by heat and pungent agents including capsaicin, and has been exten...
TRPV1 is well known as a sensor ion channel that transduces a potentially harmful environment into e...
The transient receptor potential vanilloid receptor type-1 ( TRPV1) is critically involved in periph...
Primary afferent pain fibers (nociceptors) are divided into subclasses based on distinct molecular...
Background: The transient receptor potential vanilloid subtype-1 (TRPV1) channel is a calcium select...
The transient receptor potential subfamily V member 1 (TRPV1) belongs to the diverse transient recep...
Noxious stimuli are detected by primary afferent neurons of the dorsal root ganglia (DRG). Such neur...
Acute neurogenic inflammation and pain associated to bacterial infection have been traditionally asc...
The transient receptor potential subfamily V member 1 (TRPV1) belongs to the diverse transient recep...
Transient receptor potential cation channel, subfamily V, member 1 (TRPV1, also known as vanilloid r...
Neuropathic pain and allodynia may arise from sensitization of central circuits. We report a mechani...
The capsaicin receptor TRPV1 has been widely characterized in the sensory system as a key component ...
During neuropathic pain, caspases are activated in the limbic cortex. We investigated the role of TR...
During neuropathic pain, caspases are activated in the limbic cortex. We investigated the role of TR...
Although activation of spinal glia has been implicated in the development of pathological pain, the ...
TRPV1 is an ion channel activated by heat and pungent agents including capsaicin, and has been exten...
TRPV1 is well known as a sensor ion channel that transduces a potentially harmful environment into e...
The transient receptor potential vanilloid receptor type-1 ( TRPV1) is critically involved in periph...
Primary afferent pain fibers (nociceptors) are divided into subclasses based on distinct molecular...
Background: The transient receptor potential vanilloid subtype-1 (TRPV1) channel is a calcium select...
The transient receptor potential subfamily V member 1 (TRPV1) belongs to the diverse transient recep...
Noxious stimuli are detected by primary afferent neurons of the dorsal root ganglia (DRG). Such neur...
Acute neurogenic inflammation and pain associated to bacterial infection have been traditionally asc...
The transient receptor potential subfamily V member 1 (TRPV1) belongs to the diverse transient recep...
Transient receptor potential cation channel, subfamily V, member 1 (TRPV1, also known as vanilloid r...
Neuropathic pain and allodynia may arise from sensitization of central circuits. We report a mechani...