Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2024 Jul 17:15:1435220.
doi: 10.3389/fphys.2024.1435220. eCollection 2024.

Targeting heme in sickle cell disease: new perspectives on priapism treatment

Affiliations
Review

Targeting heme in sickle cell disease: new perspectives on priapism treatment

Tammyris Helena Rebecchi Silveira et al. Front Physiol. .

Abstract

Men with sickle cell disease (SCD) frequently experience priapism, defined as prolonged, painful erections occurring without sexual arousal or desire. This urological emergency can lead to penile fibrosis and permanent erectile dysfunction if not treated adequately. Due to its complex pathophysiology, there is currently no effective preventative treatment for this condition. Recent studies have highlighted the dysfunction of the nitric oxide (NO) and cyclic guanosine monophosphate (cGMP) pathway in erectile tissues as a critical mechanism in developing priapism in SCD. Additionally, further research indicates that intravascular hemolysis promotes increased smooth muscle relaxation in the corpus cavernosum and that excess heme may significantly contribute to priapism in SCD. Pharmacological treatments should ideally target the pathophysiological basis of the disease. Agents that reduce excess free heme in the plasma have emerged as potential therapeutic candidates. This review explores the molecular mechanisms underlying the excess of heme in SCD and its contribution to developing priapism. We discuss pharmacological approaches targeting the excess free heme in the plasma, highlighting it as a potential therapeutic target for future interventions in managing priapism.

Keywords: corpus cavernosum; haptoglobin; heme; heme oxygenase; hemopexin.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
Hemopexin as a candidate for priapism prevention in SCD.

Similar articles

Cited by

References

    1. Adeyoju A. B., Olujohungbe A. B. K., Morris J., Yardumian A., Bareford D., Akenova A., et al. (2002). Priapism in sickle-cell disease; incidence, risk factors and complications - an international multicentre study. BJU Int. 90, 898–902. 10.1046/j.1464-410x.2002.03022.x - DOI - PubMed
    1. Alvaia M. A., Maia H. A. A. da S., Nelli A. de M., Guimarães C. O. S., Carvalho E. S. de S., Netto J. M. B., et al. (2020). Prevalence of priapism in individuals with sickle cell disease and implications on male sexual function. Einstein (Sao Paulo) 18, eAO5070. 10.31744/einstein_journal/2020AO5070 - DOI - PMC - PubMed
    1. Andersson K.-E. (2011). Mechanisms of penile erection and basis for pharmacological treatment of erectile dysfunction. Pharmacol. Rev. 63, 811–859. 10.1124/pr.111.004515 - DOI - PubMed
    1. Anele U. A., Le B. V., Resar L. M. S., Burnett A. L. (2015). How I treat priapism. Blood 125, 3551–3558. 10.1182/blood-2014-09-551887 - DOI - PMC - PubMed
    1. Anele U. A., Mack A. K., Resar L. M. S., Burnett A. L. (2014). Hydroxyurea therapy for priapism prevention and erectile function recovery in sickle cell disease: a case report and review of the literature. Int. Urol. Nephrol. 46, 1733–1736. 10.1007/s11255-014-0737-7 - DOI - PMC - PubMed

LinkOut - more resources