Erectile response to acute and chronic occlusion of the internal pudendal and penile arteries
- PMID: 2913367
- DOI: 10.1016/s0022-5347(17)40782-8
Erectile response to acute and chronic occlusion of the internal pudendal and penile arteries
Abstract
We designed two animal experiments to elucidate the effect of obstruction of the internal pudendal artery on erectile function. In five dogs the internal pudendal or penile artery was acutely clamped unilaterally or bilaterally with a non-crushing vascular clamp. In eight dogs, the internal pudendal or penile artery was ligated, unilaterally or bilaterally, and occlusion was maintained for two months. In both models, electrodes were implanted around the cavernous nerves for electroerection. In unilateral occlusion, blood flow in the contralateral internal pudendal artery was recorded via an ultrasonic probe. In both unilateral and bilateral occlusion, intracavernous pressure in both corpora cavernosa was recorded through a 21-gauge butterfly needle connected to a Statham transducer. In the chronic model, selective pudendal angiography was done after the erection study was completed; the dogs were then sacrificed and the penile tissue was examined histologically under light microscopy. Unilateral acute clamping of the internal pudendal or penile artery caused a compensatory increase in arterial flow in the contralateral pudendal artery with only moderate impairment of intracavernous pressure on the ipsilateral side, but bilateral occlusion resulted in a marked reduction in the intracavernous pressure response to neurostimulation. In contrast, chronic obstruction of penile vessels had a minimal effect on erectile function due to the development of a rich network of collaterals around the penis. Histological evaluation revealed mild local changes in the cavernous tissue with characteristic compensatory enlargement of branches of the cavernous artery on the control side in cases of unilateral occlusion.
Similar articles
-
The effect of venous incompetence and arterial insufficiency on erectile function: an animal model.J Urol. 1990 Sep;144(3):790-3. doi: 10.1016/s0022-5347(17)39593-9. J Urol. 1990. PMID: 2388351
-
Cavernous vein arterialization for vasculogenic impotence. An animal model.Urology. 1990 Jun;35(6):513-8. doi: 10.1016/0090-4295(90)80106-w. Urology. 1990. PMID: 2353378
-
The effect of cigarette smoking on penile erection.J Urol. 1987 Aug;138(2):438-41. doi: 10.1016/s0022-5347(17)43181-8. J Urol. 1987. PMID: 3599273
-
Arteriogenic erectile impotence.Dan Med Bull. 1986 Jun;33(3):134-50. Dan Med Bull. 1986. PMID: 3522113 Review.
-
Evidence based assessment of erectile dysfunction.Int J Impot Res. 1998 May;10 Suppl 2:S64-73; discussion S77-9. Int J Impot Res. 1998. PMID: 9647964 Review.
Cited by
-
Molecular and Histologic Evidence of Novel Erectile Dysfunction Rat Model as an Aging Atherosclerosis Model: A Preliminary Study.World J Mens Health. 2020 Jul;38(3):345-352. doi: 10.5534/wjmh.190031. Epub 2019 Jun 14. World J Mens Health. 2020. PMID: 31385467 Free PMC article.
-
Resection and Reconstruction of Giant Abdominoscrotal Arteriovenous Malformation.Plast Reconstr Surg Glob Open. 2020 Mar 27;8(3):e2725. doi: 10.1097/GOX.0000000000002725. eCollection 2020 Mar. Plast Reconstr Surg Glob Open. 2020. PMID: 32537371 Free PMC article.
-
Galectin-3 is involved in inflammation and fibrosis in arteriogenic erectile dysfunction via the TLR4/MyD88/NF-κB pathway.Cell Death Discov. 2024 Feb 20;10(1):92. doi: 10.1038/s41420-024-01859-x. Cell Death Discov. 2024. PMID: 38378809 Free PMC article.
-
Mesenchymal stem cell-derived exosomes ameliorate erection by reducing oxidative stress damage of corpus cavernosum in a rat model of artery injury.J Cell Mol Med. 2019 Nov;23(11):7462-7473. doi: 10.1111/jcmm.14615. Epub 2019 Sep 11. J Cell Mol Med. 2019. PMID: 31512385 Free PMC article.
-
Protection of nontarget structures in prostatic artery embolization.Radiol Bras. 2022 Jan-Feb;55(1):6-12. doi: 10.1590/0100-3984.2021.0021. Radiol Bras. 2022. PMID: 35210658 Free PMC article.
MeSH terms
LinkOut - more resources
Full Text Sources