Archives of Sexual Behavior

, Volume 19, Issue 3, pp 193–209 | Cite as

Enhanced sexual behavior in exercising men

  • James R. White
  • David A. Case
  • D. McWhirter
  • A. M. Mattison


The effects of 9 months of aerobic exercise on aerobic work capacity (physical fitness), coronary heart disease risk factors, and sexuality were studied in 78 sedentary but healthy men (mean age, 48 years). The men exercised in supervised groups 60 min per day, 3.5 days per week on average. Peak sustained exercise intensity was targeted at 75–80% of maximum aerobic working capacity. A control group of 17 men (mean age, 44 years) participated in organized walking at a moderate pace 60 min per day, 4.1 days per week on average. Each subject maintained a daily diary of exercise, diet, smoking, and sexuality during the first and last months of the program. Beneficial effects of chronic, vigorous exercise on fitness and coronary heart disease risk factors were obtained in close agreement with prior studies. Analysis of diary entries revealed significantly greater sexuality enhancements in the exercise group (frequency of various intimate activities, reliability of adequate functioning during sex, percentage of satisfying orgasms, etc.). Moreover, the degree of sexuality enhancement among exercisers was correlated with the degree of their individual improvement in fitness.

Key words

male sexuality exercise coronary heart disease risk factors erectile dysfunction smoking anxiety sexual arousal 


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  1. Baldwin, K., Winder, W., Terjung, R., and Holloszy, J. (1972). Glycolytic capacity of red, white, and intermediate muscle: Adaptive response to running.Med. Sci. Sport Exercise 4: 50.Google Scholar
  2. Barlow, D. H. (1986). Causes of sexual dysfunction: The role of anxiety and cognitive interference.J. Consult. Clin. Psychol. 54: 140–148.PubMedGoogle Scholar
  3. Barlow, D. H., Sakheim, D. K., and Beck, J. G. (1983). Anxiety increases sexual arousal.J. Abn. Pshycol. 92: 49–54.Google Scholar
  4. Beach, F. A. (1965). Retrospect and prospect. In Beach, F. A. (ed.),Sex and Behavior Wiley, New York, pp. 535–569.Google Scholar
  5. Beck, J. G., and Barlow, D. H. (1984). Current conceptualizations of sexual dysfunction: A review and an alternative perspective.Clin. Psychol. Rev. 4: 363–378.Google Scholar
  6. Blankenhorn, D. H. (1981). Will atheroma regress with diet and exercise?Am. J. Surg. 141: 644–645.PubMedGoogle Scholar
  7. Braude, M. C., and Morrison, J. M. (1976). Preclinical toxicity studies of naltrexone.Nat. Inst. Drug Abuse Res. Monogr. Ser. 9: 16–26.Google Scholar
  8. Brisson, G. R., Volle, M. A., Desharnais, M., Dion, M., and Tanako, M. (1977). Pituitarygonadal axis in exercising man.Med. Sci. Sport Exercise 9: 47.Google Scholar
  9. Clausen, J. P. (1976). Circulatory adjustments to dynamic exercise and effects of physical training in normal subjects and patients with coronary artery disease.Progr. Cardiovasc. Dis. 18: 459–495.Google Scholar
  10. Cumming, D. C., Brunsting, L. A., Strich, G., Ries, A. L., and Rebar, R. W. (1986). Reproductive hormone increases in response to acute exercise in men.Med. Sci. Sport Exercise 18: 369–373.Google Scholar
  11. Cumming, D. C., Wall, S. R., Galbraith, M. A., and Belcastro, A. N. (1987). Reproductive hormone responses to resistance exercise.Med. Sci. Sport Exercise 19: 234–238.Google Scholar
  12. De Lignieres, B., Plas, J-N., Commandre, F., Morville, R., Viani, J-L., and Plas, L. (1976). Secretion testiculaire d'androgenes apres effort physique prolongue chez l'homme.Nouvelle Presse Med. 5: 2060–2064.Google Scholar
  13. Dessypris, A., Kuopposalmi, K., and Adlercreutz, H. (1976). Plasma cortisol, testosterone, androstenedione, and luteinizing hormone (LH) in a non-competitive marathon run.J. Steroid Biochem. 7: 33–37.PubMedGoogle Scholar
  14. Dowell, R. T. (1983). Cardiovascular physiology of exercise. In Pollock, M., Wilmore, J., and Fox, S., III (eds.),Exercise in Health and Disease: Evaluation and Prescription for Prevention and Rehabilitation W. B. Saunders, Philadelphia, pp. 19–27.Google Scholar
  15. Dressendorfer, R. H., Wade, C. E., and Iverson, D. (1987). Decreased plasma testosterone in overtrained runners.Med. Sci. Sport Exercise 19 (Suppl.): 62.Google Scholar
  16. Forsberg, L., Gustavii, B., Hojerback, T., and Olsson, A. M. (1979). Impotence, smoking andβ-blocking drugs.Fertil. Steril. 31: 589–591.PubMedGoogle Scholar
  17. Galbo, H., Hummer, L., Petersen, L. B., Christensen, N. J., and Bie, N. (1977). Thyroid and testicular responses to graded and prolonged exercise in man.Eur. J. Appl. Physiol. Occup. Physiol. 36: 101–106.PubMedGoogle Scholar
  18. Gilbert, D. G., Hagen, R. L., and D'Agostino, J. A. (1986). The effects of smoking on human sexual potency.Addictive Behav. 11: 431–434.Google Scholar
  19. Goldstein, A., and Hansteen, R. W. (1977). Evidence against involvement of endorphins in sexual arousal and orgasm in man.Arch. Gen. Psychiat. 34: 1179–1180.PubMedGoogle Scholar
  20. Gollnick, P., Armstrong, R., Saltin, B., Saubert, C., Sembrowich, W., and Shepherd, R. (1973). Effect of training on enzyme activity and fiber composition of human skeletal muscle.J. Appl. Physiol. 34: 107–111.PubMedGoogle Scholar
  21. Guyton, A. C., Jones, C. E., and Coleman, T. G. (1973).Circulatory Physiology: Cardiac Output and Its Regulation, 2nd ed. W. B. Saunders, Philadelphia.Google Scholar
  22. Holloszy, J. (1973). Adaptations of skeletal muscle to endurance exercise: Anaerobic metabolism. In Wilmore, J. (ed.),Exercise and Sports Sciences Reviews Academic Press, New York, pp. 46–71.Google Scholar
  23. Juenemann, K-P., Lue, T. F., Luo, J-A., Benowitz, L., Abozeid, M., and Tanagho, E. A. (1987). The effects of cigarette smoking on penile erection.J. Urol. 138: 438–441.PubMedGoogle Scholar
  24. Kannel, W. B., Sorlie, P., and McNamara, P. (1971). The relation of physical activity to risk of coronary heart disease: The Framingham study. In Larson, O. A., and Malmborg, R. O. (eds.),Coronary Heart Disease and Physical Fitness University Park Press, Baltimore, MD.Google Scholar
  25. Kaplan, H. S. (1979).Disorders of Sexual Desire Simon and Schuster, New York.Google Scholar
  26. Kuopposalmi, K., Naveri, H., Rehunen, S., Harkonen, M., and Adlercreutz, H. (1976). Effect of strenuous anaerobic running exercise on plasma growth hormone, cortisol, luteinizing hormone, testosterone, androstendedione, estrone, and estradiol.J. Steroid Biochem. 7: 823–829.PubMedGoogle Scholar
  27. Lamb, D. R. (1975). Androgens and exercise.Med. Sci. Sport Exercise 7: 1–5.Google Scholar
  28. Mandell, A. (1979). The second wind.Psychiat. Ann. 9: 153–160.Google Scholar
  29. Masters, W., and Johnson, V. (1970).Human Sexual Inadequacy Little, Brown, Boston.Google Scholar
  30. Mendlson, J. H., Ellingboe, J., Keuhnle, J. C., and Mello, N. K. (1979). Effects of naltrexone on mood and neuroendocrine function in normal adult males.Psychoneuroendocrinology 3: 231–236.Google Scholar
  31. Meyerson, B. J., and Terenius, L. (1977). Beta-endorphin and male sexual behavior.Eur. J. Pharm. 42: 191–192.Google Scholar
  32. Mirin, S. M., Mendelson, J. H., Ellingboe, J., and Meyer, R. E. (1976). Acute effects of heroin and naltrexone on testosterone and gonadotrophin secretion: A pilot study.Psychoneuroendocrinology. 1: 359–369.Google Scholar
  33. Morgan, T., Cobb, L., Short, F., Ross, R., and Gunn, D. (1971). Effects of long-term exercise on human muscle mitochondria. In Pernow, B., and Saltin, B. (eds),Muscle Metabolism During Exercise Plenum Press, New York, pp. 87–95.Google Scholar
  34. Morville, R., Pesuies, P. C., Guezzennec, C. Y., Serrurier, B. D., and Guignard, M. (1979). Plasma variations in testicular and adrenal androgens during prolonged physical exercise in man.Ann. Endocrinol. 40: 501–510.Google Scholar
  35. Naughton, J., and Hellerstein, H. (1973).Exercise Testing and Training in Coronary Heart Disease Academic Press, New York.Google Scholar
  36. Sutton, J. R., Coleman, M. J., Casey, J., and Lazarus, L. (1973). Androgen responses during physical exercise.Br. Med. J. 1: 520–522.PubMedGoogle Scholar
  37. Sutton, J. R., Coleman, M. J., Casey, J. H. (1978). Testosterone production rate during exercise. In Landry, F., and Orban, W. A. R. (eds.),Third International Symposium on Biochemistry of Exercise, Book 3, Symposium Specialists, Miami, FL.Google Scholar
  38. Taylor, J. (1953). A personality scale of manifest anxiety.J. Abn. Soc. Psychol. 48: 285–290.Google Scholar
  39. Tiefer, L. (1978). Content and consequences of contemporary sex research: A feminist perspective. In McGill, T. E., Dewsbury, D. A., and Sachs, B. D. (eds.),Sex and Behavior: Status and Prospectus Plenum Press, New York, pp. 363–385.Google Scholar
  40. Virag, R., Bouilly, P., and Frydman, D. (1985). Is impotence an arterial disorder?Lancet 1: 181–184.PubMedGoogle Scholar
  41. Wahren, J., Felig, P., Ahlborg, G., and Jorfeldt, L. (1971). Glucose metabolism during leg exercise in man.J. Clin. Inv. 50: 2715–2725.Google Scholar
  42. Wheeler, G. D., Wall, S. R., Belcastro, A. N., and Cumming, D. C. (1984). Reduced serum testosterone and prolactin levels in male distance runners.J. Am. Med. Assoc. 252: 514–516.Google Scholar
  43. White, J. R. (1986).The National Health Test Goldfield Publications, La Jolla, CA.Google Scholar
  44. Wilkerson, J. E., Horvath, S. M., and Gutin, B. (1980). Plasma testosterone during treadmill exercise,J. Appl. Physiol. 49: 249–253.PubMedGoogle Scholar

Copyright information

© Plenum Publishing Corporation 1990

Authors and Affiliations

  • James R. White
    • 1
  • David A. Case
    • 2
  • D. McWhirter
    • 3
  • A. M. Mattison
    • 3
  1. 1.Physical Education Department, C-017University of CaliforniaSan Diego, La JollaUSA
  2. 2.Department of PsychologyUniversity of CaliforniaSan Diego, La JollaUSA
  3. 3.School of MedicineUniversity of CaliforniaSan Diego, La JollaUSA

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