Differential effects of superior and inferior spermatic nerves on testosterone secretion and spermatic blood flow in cats

Citation
Sr. Chiocchio et al., Differential effects of superior and inferior spermatic nerves on testosterone secretion and spermatic blood flow in cats, ENDOCRINOL, 140(3), 1999, pp. 1036-1043
Citations number
33
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
ENDOCRINOLOGY
ISSN journal
00137227 → ACNP
Volume
140
Issue
3
Year of publication
1999
Pages
1036 - 1043
Database
ISI
SICI code
0013-7227(199903)140:3<1036:DEOSAI>2.0.ZU;2-E
Abstract
It has been postulated that testosterone secretion is partially regulated b y signals from the spermatic nerves. To further examine this hypothesis in vivo, the superior (SSN) or the inferior (ISN) spermatic nerves were stimul ated electrically (varying intensity, 25 Hz, 0.2 msec, 10 min) in anestheti zed cats, determining the testosterone concentration and the blood flow in the spermatic vein. In some additional experiments arterial blood was sampl ed, and norepinephrine (NE) output was calculated. Stimulation of the SSN ( 25-35 V) increased the testosterone concentration in spermatic vein blood ( P < 0.01 compared with prestimulation levels). The response varied among an imals, reaching a 50-100% increase in some animals, whereas in others it ra nged from almost undetectable to more than 10 ng/100 g.min. Under the same experimental conditions, the NE output increased from 135.4 +/- 99 to 1614. 2 +/- 347 pg/ml (P < 0.01), and spermatic blood flow decreased from 24.1 +/ - 1.42 to 20.2 +/- 1.65 ml/min.100 g (P < 0.05) during nerve stimulation. B y contrast, stimulation of the ISN (25-35 V) modified neither the testoster one concentration, the NE output, nor the blood flow in the spermatic vein. High intensity stimulation (36-70 V) of each spermatic nerve evoked differ ent vascular and hormonal effects. SSN activation induced a marked decrease in spermatic blood flow during stimulation and an increase in the testoste rone response, whereas ISN activation resulted only in an enhanced spermati c blood flow. Our results suggest that testosterone secretion, although mai nly dependent on gonadotropin secretion, could be further regulated by neur al inputs from the SSN acting directly or alternatively through changes in blood flow. It would appear that the SSN mainly supplies the vasoconstricto r fibers to the testis, whereas the ISN provides vasodilator fibers.