In Vitro and in Vivo Demonstration of the Beneficial Effects of a Caesalpinia sappan Seeds Extract on Human Skin: From ROS Scavenging to Dark Spot Bleaching
Background:Caesalpinia sappan seeds have recently shown beneficial effects on human health because of its content in anti-inflammatory and antioxidant compounds. Reasoning that these compounds could also display beneficial effects on human skin, we investigate the antioxidant power of a Caesalpinia sappan seeds extract and its ability to protect skin against oxidative attacks. Additionally, as inflammation is often related to oxidative bursts, we evaluate the potency of our extract to act on inflammation. Finally, as our Caesalpinia sappan seeds extract is particularly rich in 4-methyl-catechol, a well-known divalent cation chelator, we test its ability to reduce tyrosinase activity which depends on the presence of copper ions, and by this way to produce any significant whitening effect on human skin. Materials and Methods: In the first part of our study, intrinsic potential of our Caesalpinia sappan seeds extract was evaluated by using a paramagnetic radical, i.e. the DiPhenl Pricryl Hydrazyl (DPPH), which emits specific colorations following its oxidation state. For the second time, we took advantage of our original model of enrichment of epidermis cell cultures in progenitor cells to show the ability of our extract to protect progenitor cells against UV irradiations. Subsequently, the potency of our Caesalpinia sappan seeds extract to inhibit Lysyl Oxidase (LOX) activity was evaluated in an in vitro model composed by a purified human enzyme. Concerning the putative whitening effect of our Caesalpinia sappan seeds extract, it was assessed in several steps: 1) measurement of its inhibitory effect on tyrosinase activity in an in vitro acellular model calling for a mushroom enzyme, 2) measurement of its inhibitory effect on melanogenesis in a model of human normal melanocytes, and at last 3) assessment of its whitening effect, and notably its bleaching effect on dark spots, in an in vivo model calling for human volunteers. Results: Our Caesalpinia sappan seeds extract strongly inhibited DPPH oxidation from 33.2 +/? 4.9% to 97.1 +/? 0.5% for Caesalpinia sappan seeds concentrations from 0.01 to 1% (v/v), respectively. As a consequence, Caesalpinia sappan seeds extract was able to efficiently protect cutaneous progenitor cells against UVB radiations from 51.1 +/? 1.7% to 86.2 +/? 3.8% of protection for Caesalpinia sappan seeds
References
[1]
Sasongko, H., Hedianti, D.P. and Safitri, L.I. (2024) Caesalpinia sappan Reduce Fever with an Anti-Inflammatory and Antioxidant Mechanism: A Review. JPSCR: Journal of Pharmaceutical Science and Clinical Research, 9, 118-139. https://doi.org/10.20961/jpscr.v9i1.79562
[2]
Konečný, L., Lomozová, Z., Karabanovich, G., Roh, J., Vávrová, K. and Mladěnka, P. (2024) Rapid Method for Screening of Both Calcium and Magnesium Chelation with Comparison of 21 Known Metal Chelators. JBIC Journal of Biological Inorganic Chemistry, 29, 785-800. https://doi.org/10.1007/s00775-024-02078-6
[3]
Wojcieszyńska, D., Hupert-Kocurek, K., Jankowska, A. and Guzik, U. (2012) Properties of Catechol 2,3-Dioxygenase from Crude Extract of Stenotrophomonas Maltophilia Strain KB2 Immobilized in Calcium Alginate Hydrogels. Biochemical Engineering Journal, 66, 1-7. https://doi.org/10.1016/j.bej.2012.04.008
[4]
Rouzer, C.A. and Samuelsson, B. (1987) Reversible, Calcium-Dependent Membrane Association of Human Leukocyte 5-Lipoxygenase. Proceedings of the National Academy of Sciences of the United States of America, 84, 7393-7397. https://doi.org/10.1073/pnas.84.21.7393
[5]
Solano, F. (2018) On the Metal Cofactor in the Tyrosinase Family. International Journal of Molecular Sciences, 19, Article 633. https://doi.org/10.3390/ijms19020633
[6]
Meunier, M., Bracq, M., Chapuis, E., Lapierre, L., Humeau, A., Bernard, S., et al. (2023) Targeting SDF-1 as an Efficient Strategy to Resolve Skin Hyperpigmentation Issues with Himanthalia elongata Extract. Journal of Cosmetic Dermatology, 22, 383-394. https://doi.org/10.1111/jocd.15357
[7]
Gulcin, İ. (2020) Antioxidants and Antioxidant Methods: An Updated Overview. Archives of Toxicology, 94, 651-715. https://doi.org/10.1007/s00204-020-02689-3
[8]
Goodell, M.A., Brose, K., Paradis, G., Conner, A.S. and Mulligan, R.C. (1996) Isolation and Functional Properties of Murine Hematopoietic Stem Cells That Are Replicating in Vivo. The Journal of experimental medicine, 183, 1797-1806. https://doi.org/10.1084/jem.183.4.1797
[9]
Durand, R.E. and Olive, P.L. (1982) Cytotoxicity, Mutagenicity and DNA Damage by Hoechst 33342. Journal of Histochemistry & Cytochemistry, 30, 111-116. https://doi.org/10.1177/30.2.7061816
[10]
Nakai, K. and Tsuruta, D. (2021) What Are Reactive Oxygen Species, Free Radicals, and Oxidative Stress in Skin Diseases? International Journal of Molecular Sciences, 22, Article 10799. https://doi.org/10.3390/ijms221910799
[11]
Krieg, P. and Fürstenberger, G. (2014) The Role of Lipoxygenases in Epidermis. Biochimica et Biophysica Acta (BBA)—Molecular and Cell Biology of Lipids, 1841, 390-400. https://doi.org/10.1016/j.bbalip.2013.08.005
[12]
Xue, T., Lu, Z., Zhang, W., Wang, Z., Shi, Y., Jiang, H., et al. (2022) Facial Erythema Due to Lupus Vulgaris and Candida albicans Infections: A Case Report. Clinical, Cosmetic and Investigational Dermatology, 15, 1397-1402. https://doi.org/10.2147/ccid.s372359
[13]
Scherdin, U., Bürger, A., Bielfeldt, S., Filbry, A., Weber, T., Schölermann, A., et al. (2008) Skin-Lightening Effects of a New Face Care Product in Patients with Melasma. Journal of Cosmetic Dermatology, 7, 68-75. https://doi.org/10.1111/j.1473-2165.2008.00364.x
[14]
Elvebakken, H.F., Christensen, I.B., Vedel, C. and Kjærulff, S. (2024) A Proof of Concept: Clinical Anti‐aging Efficacy and Safety of Lactiplantibacillus plantarum LB244R® Applied Topically in a Double-Blinded Placebo-Controlled Study. Journal of Cosmetic Dermatology, 23, 1233-1242. https://doi.org/10.1111/jocd.16138
[15]
Bradford, M.M. (1976) A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye Binding. Analytical Biochemistry, 72, 248-254. https://doi.org/10.1016/0003-2697(76)90527-3
[16]
Lemaitre, J. (2024) Looking for the Philosopher’s Stone: Emerging Approaches to Target the Hallmarks of Aging in the Skin. Journal of the European Academy of Dermatology and Venereology, 38, 5-14. https://doi.org/10.1111/jdv.19820
[17]
Kim, S.Y., Kim, T., Moon, K., Kim, T.J., Shin, D., Cho, Y.S., et al. (2008) Regulation of Pro-Inflammatory Responses by Lipoxygenases via Intracellular Reactive Oxygen Species in Vitro and in Vivo. Experimental and Molecular Medicine, 40, 461-476. https://doi.org/10.3858/emm.2008.40.4.461
[18]
Smelly, M. and Hawkey, C. (2003) Cox-Lox Inhibition: Current Evidence for an Emerging New Therapy. International Journal of Clinical Practice, 57, 301-304. https://doi.org/10.1111/j.1742-1241.2003.tb10489.x
[19]
Hammarberg, T., Reddy, K.V., Persson, B. and Rádmark, O. (2002) Calcium Binding to 5-Lipoxygenase. In: Honn, K.V., Marnett, L.J., Nigam, S., Dennis, E. and Serhan, C., Eds., Eicosanoids and Other Bioactive Lipids in Cancer, Inflammation, and Radiation Injury, 5., Springer, 117-121. https://doi.org/10.1007/978-1-4615-0193-0_19
[20]
Sharma, H.K. and Vaidyanathan, C.S. (1975) A New Mode of Ring Cleavage of 2,3‐dihydroxybenzoic Acid in Tecoma stans (L.). European Journal of Biochemistry, 56, 163-171. https://doi.org/10.1111/j.1432-1033.1975.tb02219.x
[21]
Rinnerthaler, M., Bischof, J., Streubel, M., Trost, A. and Richter, K. (2015) Oxidative Stress in Aging Human Skin. Biomolecules, 5, 545-589. https://doi.org/10.3390/biom5020545
[22]
Kehrer, J.P. (2000) The Haber-Weiss Reaction and Mechanisms of Toxicity. Toxicology, 149, 43-50. https://doi.org/10.1016/s0300-483x(00)00231-6