R. Tamura et al., SEGMENTAL DISTRIBUTION OF AFFERENT NEURONS INNERVATING THE CANINE TESTIS, Journal of the autonomic nervous system, 58(1-2), 1996, pp. 101-107
To clarify the afferent innervation of the canine scrotal contents, re
trograde labeling of neurons in the dorsal root ganglia (DRG) has been
carried out using two methods: (1) horseradish peroxidase (HRP) injec
tion into the surface of the testis and epididymis; and (2) exposure o
f the superior spermatic nerve to a fluorescent dye (Fast blue; FB). I
njections of HRP resulted in labeling of DRG cells located predominant
ly from T10 to L4 (87%) and, to a lesser extent, at S1-S3 (13%), Trans
ection of the vas deferens previous to testicular injections eliminate
d labeling in the S1-S3 DRG, but not at thoracolumbar levels. These fi
ndings indicated that primary afferent fibers of the testis and epidid
ymis project mainly to the DRG at higher than L4 through the superior
spermatic nerve, but an additional population of the fibers also proje
cts the sacral level through the inferior spermatic nerve. Exposure of
the superior spermatic nerve to FB resulted in a; similar distributio
n of labeled cells as compared with testicular injections of HRP after
vasectomy. Labeled cells (8.1%) were also observed in the contralater
al T13-L3 DRG, In both FB and HRP groups, the major part of the labele
d cells was located in L1 and L2. The sizes of HRP- and FB-labeled cel
ls were smaller than those of unlabeled cells in the L1 and 1,2 DRG. T
he cumulative frequency distribution histogram for the diameter of HRP
- and FB-labeled cells could be fitted by a normal distribution.