Fc. Tanyel et al., Mechanisms involved in contractile differences among cremaster muscles according to localization of testis, J PED SURG, 36(10), 2001, pp. 1551-1560
Background/Purpose: Evidence suggests differences in contractility in crema
ster muscles (CM) associated with undescended testis caused by alterations
of autonomic innervation. Contractile responses of CM to various pharmacolo
gic agents were evaluated and compared according to the localization of tes
tis.
Methods: Samples of CM from boys with undescended testis or inguinal hernia
were obtained. Twitch and tetanic contractions were recorded isometrically
at 37 degreesC. Effects of verapamil, isoprenaline, calcitonin gene-relate
d peptide (CGRP), substance P (SP) and N-omega-nitro-L-arginine (L-NNA) wer
e investigated.
Results were compared through 2-way analysis of variance, and P values less
than .05 were considered to be different. Results: Verapamil alone signifi
cantly (P < .05) decreased contraction amplitudes in CM from both sources;
the decrease was more pronounced in CM from boys with inguinal hernia (P <
.05). Although isoprenaline increased contraction amplitudes in CM associat
ed with undescended testis (P < .05), CGRP and SP increased contraction amp
litudes in CM associated with descended testis (P < .05). L-NNA increased c
ontraction amplitudes in both groups (P < .05). The decrease of contraction
amplitudes after verapamil displayed a similar pattern after isoprenaline,
SP, and L-NNA. Verapamil-induced contractility decrease was more pronounce
d after CGRP in both groups (P < .05).
Conclusions: Sensitivity of CM to verapamil differs according to localizati
on of testis. Isoprenaline enhances contractility by stimulating Na+-K(+)AT
Pase in undescended testis without altering voltage-sensitive channel sensi
tivity to verapamil. CGRP and SP increase contractility in inguinal hernia,
and CGRP increases the sensitivity of voltage-sensitive Ca2+ channels to v
erapamil in CM from both groups. Nitric Oxide (NO) exerts inhibitory action
on CM contractility, and it is less pronounced in undescended testis. Thes
e differences may contribute to pathophysiology of undescended testis. Copy
right (C) 2001 by W.B. Saunders Company.