H. Danuser et al., EXTRINSIC INNERVATION OF THE CAT PROSTATE-GLAND - A COMBINED TRACING AND IMMUNOHISTOCHEMICAL STUDY, The Journal of urology, 157(3), 1997, pp. 1018-1024
Purpose: The purpose of the present study was to determine the periphe
ral neural pathways, spinal distribution, sizes, and peptide transmitt
er content of primary afferent and autonomic efferent neurons that inn
ervate the prostate gland. Methods: Retrograde transport of the fluore
scent dye ''fast blue'' (injected into the prostate gland) was combine
d with neurotransmitter immunohistochemistry. Lesions of the pelvic an
d pudendal nerve were used to determine the peripheral neural pathways
. Results: The majority of the afferent innervation arose from the sac
ral dorsal root ganglia (DRG) and was equally comprised of small, subs
tance P- and calcitonin gene-related peptide-immunoreactive (IR) neuro
ns and large, non-IR neurons. The majority (70%) of the afferent axons
traversed the pelvic nerve with the remainder traversing the pudendal
nerve. Fewer afferent neurons were located in lumbar DRG; nearly all
of these were small, peptidergic neurons. Efferent autonomic neurons w
ere located in the inferior mesenteric ganglia (IMG), sympathetic chai
n ganglia (SCG), and pelvic plexus ganglia (PPG). Nearly all efferent
neurons in the IMG and SCG, but only 2/3 of the PPG neurons, contained
dopamine-beta-hydroxylase. Substantial neuropeptide Y innervation was
derived from the SCG but not the IMG or PPG. Conclusions: First, clin
ical reports suggested that sensory innervation of the prostate would
be purely nociceptive in nature (implied by small, peptide-IR neurons)
. However, the present study suggests that there may also be a substan
tial, presumably non-nociceptive, afferent innervation (implied by fin
dings of large, non-IR neurons). Second, 3 sources of autonomic effere
nt innervation exist, each being different in the distribution of tran
smitter phenotypes. Understanding the physiological role of putative n
on-nociceptive primary afferent neurons, and the differential roles of
the various autonomic neurons, is likely to be important in developin
g therapies for the treatment of prostatic diseases, such as benign pr
ostatic hyperplasia and prostatodynia.