4.5 Article

Peripheral and central neuroplasticity in a mouse model of endometriosis

Journal

JOURNAL OF NEUROCHEMISTRY
Volume -, Issue -, Pages -

Publisher

WILEY
DOI: 10.1111/jnc.15843

Keywords

central neuroinflammation and sensitization; chronic pelvic pain; endometriosis; hypersensitivity; peripheral and central neuroplasticity; vagina-innervating afferents

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This study investigates the changes in sensory neurons and central nervous system processing in endometriosis patients with chronic pelvic pain. It reveals that sensory neurons innervating the reproductive tract develop mechanical hypersensitivity in endometriosis, along with neuroinflammation and sensitization of spinal circuitry. These findings provide insights into the altered pain sensitivity in endometriosis and offer a potential platform for targeted pain relief treatments.
Chronic pelvic pain (CPP) is the most debilitating symptom of gynaecological disorders such as endometriosis. However, it remains unclear how sensory neurons from pelvic organs affected by endometriosis, such as the female reproductive tract, detect and transmit nociceptive events and how these signals are processed within the central nervous system (CNS). Using a previously characterized mouse model of endometriosis, we investigated whether the increased pain sensitivity occurring in endometriosis could be attributed to (i) changes in mechanosensory properties of sensory afferents innervating the reproductive tract, (ii) alterations in sensory input from reproductive organs to the spinal cord or (iii) neuroinflammation and sensitization of spinal neural circuits. Mechanosensitivity of vagina-innervating primary afferents was examined using an ex vivo single-unit extracellular recording preparation. Nociceptive signalling from the vagina to the spinal cord was quantified by phosphorylated MAP kinase ERK1/2 immunoreactivity. Immunohistochemistry was used to determine glial and neuronal circuit alterations within the spinal cord. We found that sensory afferents innervating the rostral, but not caudal portions of the mouse vagina, developed mechanical hypersensitivity in endometriosis. Nociceptive signalling from the vagina to the spinal cord was significantly enhanced in mice with endometriosis. Moreover, mice with endometriosis developed microgliosis, astrogliosis and enhanced substance P neurokinin-1 receptor immunoreactivity within the spinal cord, suggesting the development of neuroinflammation and sensitization of spinal circuitry in endometriosis. These results demonstrate endometriosis-induced neuroplasticity occurring at both peripheral and central sites of sensory afferent pathways. These findings may help to explain the altered sensitivity to pain in endometriosis and provide a novel platform for targeted pain relief treatments for this debilitating disorder.

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