PHD, Kent State University, 2025, College of Arts and Sciences / School of Biomedical Sciences
Spinal cord injury (SCI) significantly impairs ejaculatory function, a complex reflex controlled by the spinal ejaculation generator (SEG) located in the lumbar spinal cord. In male rats, mice and humans, the SEG comprises a cluster of specialized neurons known as lumbar spinothalamic (LSt) cells, which integrate sensory inputs during sexual activity into a coordinated autonomic and motor response culminating in ejaculation. Sensory inputs, originating partially from the dorsal penile nerve (DPN), require glutamate receptor activation in LSt cells. Previous studies have established that LSt neurons express GluN1 receptor, and antagonizing these receptors disrupts DPN-induced ejaculatory reflex. This dissertation hypothesized that GluA receptor activation is also essential for sensory-induced ejaculatory reflexes in adult male rats. To test this hypothesis, fluorescent in situ hybridization (FISH) was employed to examine the expression of GluA1, 2, 3 and 4 receptor mRNA in LSt cells in sham and SCI male rats. The results showed that GluA receptors subunits are expressed in LSt cells and remained unaffected by SCI. Furthermore, the role of GluA receptors in sensory-induced ejaculation was tested using an intraspinal injection of AMPA receptor antagonist NBQX in anesthetized, spinalized rats with DPN stimulation. NBQX administration blocked DPN-induced ejaculatory reflexes at the higher, but not lower, NBQX volume, supporting the hypothesis of GluA receptor involvement in ejaculation.
In addition to peripheral sensory inputs, the SEG is influenced by supraspinal inputs from brainstem and hypothalamus areas, including dopaminergic and serotonergic projections. The dissertation also investigates the role of dopamine D3 receptors in ejaculation, hypothesizing their critical involvement in this reflex. FISH and immunofluorescence assays revealed that LSt cells co-expressed mRNA for dopamine D1, D2 and D3 receptors, with no significant alterations following SCI. Although t (open full item for complete abstract)
Committee: Lique Coolen (Advisor)
Subjects: Biomedical Research; Neurosciences; Surgery