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The effect of impaired lipid metabolism on the smooth muscle cells of rabbits

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Summary

Our clinical data enabled us to demonstrate a correlation between impaired lipid metabolism and vasculogenic impotent men. Our aim was to evaluate the effect of an impaired lipid metabolism on the smooth muscle of the corpus cavernosum. A total of 16 rabbits were given a cholesterol-enriched diet for 3 months, and 8 of these received additional thromboxane A2 receptor antagonist; 10 other rabbits (control) were fed a normal diet. Subsequently, cavernous tissue biopsies were taken, and tissue lipid extractions and electron microscopic evaluation were made from 3 rabbits in each group. In the untreated high-cholesterol diet group, cholesterol levels reached approx. 2.1 μg/mg body weight compared with 1.07 μg/mg b.wt. in the thromboxane A2 receptor antagonist-treated group and elevated levels compared with control group. Similar results were found for the triglyceride and free fatty acid levels. Lecithin tissue levels in treated rabbits were distinctly elevated against those of other 2 groups. Ultramorphological examination of the control group disclosed normal smooth muscle cell (SMC) architecture with numerous sites of intercellular contacts. These findings contrasted with those of the high-cholesterol diet groups which showed significant SMC degeneration with loss of intercellular contacts. Our data imply that impaired lipid metabolism causes cavernous SMC degeneration which plays a major role in the pathogenesis of erectile dysfunction. The thromboxane A2 receptor antagonist seems to produce a protective metabolic effect on the erectile tissue which may have some consequences future treatment strategies.

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References

  1. Anitschkow N, Chalatow S (1913) On experimental cholesteatosis and its influence on the formation of some pathologic processes (in German). Zentralbl Allg Pathol 24:1

    Google Scholar 

  2. Bergmann RA (1956) Proceedings of First European Regional Conference on Electron Microscopy, Stockholm

  3. Bouilly P, Virag R (1984) Results of a comparative study of the impotence incidence on the occasion of a medical examination and the incidence of arterial risk factors in a series of impotent subjects. In: Virag R, Virag-Lappas H (eds) Les Editions du CERI: Proceedings of the First World Meeting on Impotence, Paris, June 1984, p 23

  4. Caesar R, Edwards GA, Ruska H (1957) Architecture and nerve supply of mammalian smooth muscle tissue. J Biophys Biochem Cytol 3:867

    Google Scholar 

  5. Fournier GR Jr, Jünemann KP, Lue TF, Tanagho EA (1987) Mechanisms of venous occlusion during canine penile erection: an anatomic demonstration. J Urol 137:163

    Google Scholar 

  6. Hebrang A, Vrhovski D, Vidakovic Z, Subic N (1986) The correlation of angiographic findings and atherosclerotic risk factors in vascular impotence. Second World Meeting on Impotence, Prague, June 17–20

  7. Jünemann KP, Luo JA, Lue TF, Tanagho EA (1986) Further evidence of venous outflow restriction during erection. Bri J Urol 58:320

    Google Scholar 

  8. Jünemann KP, Persson-Jünemann C, Alken P (1990) Pathophysiology of erectile dysfunction. Semin Urol 8:80

    Google Scholar 

  9. Lue TF, Takamura T, Schmidt RA, Palubinskas AJ, Tanagho EA (1983) Hemodynamics of erection in the monkey. J Urol 130:1237

    Google Scholar 

  10. Montague DK, James RE Jr, de Wofe V (1979) Diagnostic evaluation, classification and treatment of men with sexual dysfunction. Urology 14:545

    Google Scholar 

  11. Persson C, Diederichs W, Lue TF, Yen TS, Fishman IJ, McLin PH, Tanagho EA (1989) Correlation of altered penile ultrastructure with clinical arterial evaluation. J Urol 142:1462

    Google Scholar 

  12. Persson-Jünemann C, Diedrichs W, Lue TF (1988) Correlation of impaired penile ultrastructure to quantified clinical impotence. In: Goldstein I, Krane RJ, Padma-Nathan (eds) Proceedings of the Sixth Biennial International Symposium for Corpus Cavernosum Revascularization — Third Biennial World Meeting on Impotence, Boston, MA, Oct. 6–9

  13. Bligh EG, Dyer WF (1959) Con J Biochem 37:911

    Google Scholar 

  14. Rubin A, Babbott D (1958) Impotence and diabetes mellitus. JAMA 168:498

    Google Scholar 

  15. Sarramon JP, Rischmann P, Elman B (1986) Within the last five years our experience in impotence vascular surgery. Second World Meeting on Impotence, Prague, June 17–20

  16. Virag R (1986) The screening of impotence by the use of visual sexual stimulation after intracavernous injection of a small (8 mg) dose of papaverine. Second World Meeting on Impotence, Prague, June 17–20

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Jünemann, K.P., Aufenanger, J., Konrad, T. et al. The effect of impaired lipid metabolism on the smooth muscle cells of rabbits. Urol. Res. 19, 271–275 (1991). https://doi.org/10.1007/BF00299056

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