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
. 2020 Nov 26;25(23):5557.
doi: 10.3390/molecules25235557.

Tetracyclic and Pentacyclic Triterpenes with High Therapeutic Efficiency in Wound Healing Approaches

Affiliations
Review

Tetracyclic and Pentacyclic Triterpenes with High Therapeutic Efficiency in Wound Healing Approaches

Roxana Ghiulai et al. Molecules. .

Abstract

Wounds are among the most common skin conditions, displaying a large etiological diversity and being characterized by different degrees of severity. Wound healing is a complex process that involves multiple steps such as inflammation, proliferation and maturation and ends with scar formation. Since ancient times, a widely used option for treating skin wounds are plant- based treatments which currently have become the subject of modern pharmaceutical formulations. Triterpenes with tetracyclic and pentacyclic structure are extensively studied for their implication in wound healing as well as to determine their molecular mechanisms of action. The current review aims to summarize the main results of in vitro, in vivo and clinical studies conducted on lupane, ursane, oleanane, dammarane, lanostane and cycloartane type triterpenes as potential wound healing treatments.

Keywords: pentacyclic triterpenes; tetracyclic triterpenes; wound healing.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Skin structure.
Figure 2
Figure 2
Healing cascade phases of acute wounds.
Figure 3
Figure 3
Chemical structures of lupane-skeleton triterpenes.
Figure 4
Figure 4
Chemical structures of ursane-skeleton triterpenes.
Figure 5
Figure 5
Chemical structures of oleanane-skeleton triterpenes A.
Figure 6
Figure 6
Chemical structures of oleanane-skeleton triterpenes B.
Figure 7
Figure 7
Key structural features present in all pentacyclic triterpene structures with wound healing properties (A); superimposed 3D structures of wound healing pentacyclic triterpene structures (B); areas where key functional groups appear are highlighted in yellow; structures that have glycosylated OH or COOH groups, are depicted only as triterpene scaffolds for better image clarity.
Figure 8
Figure 8
Chemical structures of dammarane-type triterpenes.
Figure 9
Figure 9
Chemical structure of cycloastragenol, a lanostane-type triterpenes.
Figure 10
Figure 10
Chemical structure of cycloartane-type triterpenes.

References

    1. Clark R.A.F. Wound repair: Basic biology to tissue engineering. In: Vacanti R., Lanza R., Langer J., editors. Principles of Tissue Engineering. 4th ed. Academic Press; London, UK: 2014. pp. 1595–1617.
    1. Nather A. The Diabetic Foot. World Scientific Pub. Co. Pte. Lt.; Singapore: 2012. pp. 89–96.
    1. Leaper D.J., Harding K.G. ABC of wound healing: Traumatic and surgical wounds. BMJ. 2006;332:532–535. doi: 10.1136/bmj.332.7540.532. - DOI - PMC - PubMed
    1. Enoch S., Leaper D.J. Basic science of wound healing. Surgery (Oxford) 2008;26:31–37. doi: 10.1016/j.mpsur.2007.11.005. - DOI
    1. Prakash G., Varma S., Malhotra P. Prevention and Management of Infections. In: Sharma A., editor. Textbook of Systemic Vasculitis. Jaypee Brothers Medical Publishers; New Delhi, India: 2015. pp. 407–412.

MeSH terms

LinkOut - more resources