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°Å¼¼µÈ Åä³¢¿¡¼­ ³²¼ºÈ£¸£¸óÅõ¿©°¡ À½°æÀÇ Nitric Oxide Synthase¿¡ ¹ÌÄ¡´Â ¿µÇâ The Effect of Testosterone on Nitric Oxide Synthase in the Penis of the Rabbit

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Abstract

¼­·Ð
À½°æ¹ß±â´Â À½°æÇظéüÆòÈ°±ÙÀÌ ÀÌ¿ÏµÇ°í ¼Ò°øÀÌ ÆØâµÇ¾î À½°æ³»¾ÐÀÌ Áõ°¡µÊ¿¡ µû¶ó À¯
¹ßµÈ´Ù. ÀÌ·¯ÇÑ À½°æ¹ß±â´Â À½°æÇظéüÆòÈ°±ÙÀÇ ±äÀå·Â¿¡ ÀÇÇØ Á¶ÀýµÇ´Â ¹Ù, ºñ¾Æµå·¹³¯¸°¼º
ºñÄݸ°¼º ½Å°æÀü´Þ¹°Áú°ú Çظéü ³»ÇǼ¼Æ÷¿¡¼­ ºÐºñµÇ´Â À̿Ϲ°ÁúÀÌ À½°æ¹ß±âÀÇ Áß½ÉÀÎ À½
°æÇظéüÆòÈ°±ÙÀÇ ÀÌ¿Ï¿¡ Áß¿äÇÑ ¿ªÇÒÀ» ÇÏ°í ÀÖÀ½ÀÌ ¹àÇôÁö°í ÀÖ´Ù. nitric oxide(NO)´Â Æò
È°±Ù ÀÌ¿ÏÀÇ »ý¸®ÇÐÀû Àü·ÉÀ¸·Î ÃÖ±Ù À½°æÇظéüÆòÈ°±Ù ÀÌ¿ÏÀÇ ÁÖ ¸Å°³Ã¼·Î ¾Ë·ÁÁö¸é¼­ À½
°æÀÇ NO¿¡ ´ëÇÑ ³²¼ºÈ£¸£¸ó ¿ªÇÒÀÌ ¿¬±¸µÇ°í ÀÖ´Ù. ±×·¯³ª ÇöÀç±îÁöÀÇ º¸°í¸¦ Åä´ë·Î ³²¼º
È£¸£¸óÀÌ À½°æÀÇ NO¿¡ ¹ÌÄ¡´Â Á÷Á¢ÀûÀÎ »óÈ£°ü°è¸¦ ÃßÁ¤Çϱâ´Â ¹ÌÈíÇÑ ½ÇÁ¤ÀÌ´Ù.
º» ¿¬±¸¿¡¼­´Â ³²¼ºÈ£¸£¸óÀÌ À½°æÀÇ NO¿¡ ¹ÌÄ¡´Â ¿µÇâÀ» °üÂûÇÏ°íÀÚ ¼º¼÷ÇÑ Åä³¢¸¦ ´ë
»óÀ¸·Î °íȯÁ¦ °Å·Î ³²¼º È£¸£¸ó °áÇÌÀ» À¯µµÇÏ°í ±â°£¿¡ µû¶ó ³²¼º È£¸£¸óÀ» º¸ÃæÇÏ¿©, ³²
¼ºÈ£¸£¸óÀÌ À½°æ¹ß±âÀÇ ÁÖ ¸Å°³Ã¼·Î ¾Ë·ÁÁø NO¿¡ ¹ÌÄ¡´Â È¿°ú¸¦ °üÂûÇÏ°íÀÚ ÇÏ¿´´Ù.

Purpose: Androgen was thought to be linked to sexual activity in man but its
peripheral action have not been identified precisely. Recently, androgens dependent nature
of nitric oxide synthase(NOS), the enzyme system producing nitric oxide(NO) as the
principal mediator in penile erection, has been studied. The present study was designed
to determine if NO within the penis is regulated by androgen.
Materials and Methods: Effect of testosterone on the penile NO was investigated from
three groups of rabbit; control(a sham operation), castration group(four sub-groups: 1, 2,
3 and 4 weeks after castration) and testosterone replacement group(four sub-groups:
testosterone propionate(10§·/day) was given subcutaneously from 1, 2, 3 and 4 weeks
after castration for 7 days respectively). Strips of rabbit corpus cavernosum were
isolated and mounted in organ chambers. The relaxation effects were assessed with
electrical field stimulation(EFS) in the precontracted cavernosal muscle strips with
phenylephrine. Penile NOS activity was measured by the rate of
14C-L-arginine-citrulline conversion. Penile tissue was subsequently
stained for the presence of NOS, using a nicotinamide adenine dinucleotide phosphate
diaphorase(NADPH-d) histochemistry.
Results: EFS evoked a relaxation of rabbit corpus cavernosum. A gradual decrease in
the EFS evoked relaxation was recorded, proportional to the duration of being castrated,
which was restored to the level of control by testosterone replacement. After castration,
penile NOS activity was significantly reduced to 51.3%, 43.7%, 37.5%, and 32.7% of the
level of control at 1, 2, 3, 4 weeks. This decrease in penile NOS activity after castration
was also restored by testosterone replacement. Diffusely scattered delicate nerve fibers
showing blue color reaction after NADPH-d histochemical staining were reduced in
castrated cavernosum in comparison with control.
Conclusions: Based on presented data we conclude that testosterone plays a direct role
in penile erection by regulating the activity of NOS within the penis.

Å°¿öµå

Testosterone; Nitric oxide; Cavernosal smooth muscle; Rabbit;

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