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Learn MoreEpigallocatechin gallate (EGCG) is a popular ingredient found in hair growth supplements, serums, & topicals. Unfortunately, there’s little clinical data showing it can regrow hair in humans, and at higher doses, it might be toxic. On the one hand, in vitro studies suggest EGCG has 5-alpha reductase inhibiting properties, and thus might improve hair growth outcomes by lowering dihydrotestosterone (DHT). On the other hand, no clinical studies exist showing that EGCG – as a standalone ingredient – promotes hair growth in men & women with androgenic alopecia. In this article, we’ll explore the data and reveal if EGCG is worth its costs.
Epigallocatechin gallate (EGCG), a compound found in green tea, is often included in serums and supplements targeted for hair growth. On the one hand, EGCG has the potential to impact a variety of diseases. As a powerful antioxidant and an antitumor agent, EGCG might have therapeutic benefit for those with diabetes, Parkinson’s disease, Alzheimer’s disease, stroke, and obesity.[1]Singh, B.N., Shankar, S., Srivastava, R.K. (2011). Green tea catechin, epigallocatechin-3-gallate (EGCG): mechanisms, perspectives and clinical applications. Biochemical Pharmacology. 82(12). … Continue reading On the other hand, the evidence on EGCG and hair regrowth is incredibly limited – particularly for men and women with pattern hair loss (androgenetic alopecia).
In this article, we will examine the potential for EGCG to impact hair follicle growth and determine whether the evidence supports its use in hair loss products.
Green tea is one of the oldest and most popular drinks in the world, mainly grown in Japan, China, and Taiwan. Full of several chemicals known as flavonoids (which includes EGCG) green tea is best known for its antioxidant, anti-inflammatory, antimicrobial, and chemoprotective properties.[3]Musial, C., Kuban-Jankowska, A., Gorska, Ponikowska, M. (2020). Beneficial properties of green tea catechins. International Journal of Molecular Science. 21(5). 1744. Available at: … Continue reading It is logical to think that some of these properties may benefit hair growth, however, is there any scientific evidence to show this?
There are some studies completed in cells and in hair follicles that elucidate some of the pathways in which EGCG exerts its effects on hair follicles.
One study determined the effect of EGCG and its derivatives on 5α-reductase activity.[4]Hiipakka, R.A., Zhang, H.Z., Dai, W., Dai, Q., Liao, S. (2002). Structure-activity relationships for inhibition of human 5α-reductases by polyphenols. Biochemical Pharmacology. 63. 1165-1176. … Continue reading In a cell-free enzyme assay, Epicatechin gallate (ECG), and EGCG were both able to effectively inhibit 5α-reductase than Epicatechin and Epigallocatechin. Furthermore, they were more effective inhibitors of Type 1 5α-reductase than Type 2 (Figure 2). However, in a whole-cell assay, none of EGCG or its derivatives has any effect, indicating that it may not be able to cross the cell barrier, and therefore might be limited in its effectiveness in animal or human studies.
Another study conducted in human dermal papilla cells examined the effects of EGCG on dihydrotestosterone-induced cell death.[6]Shin, S., Kim, K., Lee, M.J., Lee, J., Choi, S., Kim, K.S., Ko, J.M., Han, H., Kim, S.Y., Youn, H.J., Ahn, K.Y., An, I.S., An, S., Cha, H.J. (2016). Epigallocatechin gallate-mediated alteration of … Continue reading Dermal papilla cells are specialized cells involved in cell signaling and hair follicle cycling.[7]Morgan, B.A., (2014). The dermal papilla: an instructive niche for epithelial stem and progenitor cells in development and regeneration of the hair follicle. Cold Spring Harbor Perspectives in … Continue reading
Human dermal papilla cells were treated with dihydrotestosterone (DHT) and EGCG at a range of concentrations. Then the researchers conducted cell viability assays, cell cycle analysis, and intracellular reactive oxygen species assay.
Treatment with 10 µM of EGCG alone showed the highest cell viability, with a subsequent dose-dependent decrease after 20 µM (Figure 3a). Next, the researchers determined whether EGCG treatment was able to protect cells against the negative effects of DHT. The cells treated with only DHT showed a 40% reduction in cell viability, however, the 5 – 15 µM concentrations of EGCG showed a subsequent rescue in cell viability. This rescue however was not able to return cell viability levels to the control level (Figure 3b).
The researchers next determined the percentage of cells that were undergoing cell death (apoptosis), using a technique called flow cytometry. When cells are detected to be in the sub-G1 stage of the cell cycle, this means that they are undergoing apoptosis. Cells were treated with either nothing (- -), DHT alone (- +), EGCG alone (+ -), or EGCG and DHT together (+ +) (Figure 3). DHT treatment alone increased the percentage of dying cells to around 20%. EGCG treatment also increased the number of dying cells, but not to the same extent as DHT treatment. When cells were treated with EGCG and DHT together, there was a notable decrease in cell death indicating that EGCG can rescue cells from DHT-induced cell death. This was not a full rescue, however, as it returned cell death levels to that of EGCG alone, instead of levels after no treatment at all.
The effect of EGCG on levels of reactive oxygen species (ROS) inside the cell was next measured. It was found that DHT drastically increased ROS with around 45% of cells showing a positive signal (Figure 4). EGCG alone reduced the number of cells with ROS to nearly 0%, which was even lower than the no-treatment group. The group treated with EGCG and DHT together showed a reduction in ROS, with around 30% of cells showing a positive signal, however, this was still notably increased compared to the no-treatment group.
Reactive oxygen species are also one of the factors involved in the induction of senescence.[11]Lai, J.J., Chang, P., Lai, K.P., Chen, L., Chang, C. (2012). The role of androgen and androgen receptors in skin-related disorders. Archives of Dermatological Research. 304(7). 499-510. Available at: … Continue reading Cellular aging leads to a natural process known as senescence, which plays a crucial role in maintaining the balance of cellular function in our body. Senescence is characterized by a decrease in cell division and growth, but it does not necessarily indicate cell death or inactivity. Instead, senescent cells undergo a dynamic transformation in the signaling and secretion of specific markers, ultimately removing them from the body. Although this is beneficial for overall health, the buildup of senescent cells can cause chronic inflammation and lead to various diseases.[12]Hernandez-Segura, A., Nehme, J., Demaria, M. (2018). Hallmarks of cellular senescence. Trends in Cellular Biology. 28(6). 436-453. Available at: https://doi.org/10.1016/j.tcb.2018.02.001
Treatment of dermal papilla cells with DHT alone significantly increased the percentage of cells undergoing senescence to over 20% (Figure 5). Combination treatment with EGCG did lower the percentage of senescent cells to around 15% however this did not reach the same level as the untreated group.
The researchers also conducted a microarray analysis of over 1000 microRNAs (miRNAs) to determine the mechanism of action of EGCG’s protective effects against DHT. MiRNAs are a class of non-coding RNAs that play important roles in regulating gene expression.[14]O’Brian, J., Hayder, H., Zayed, Y., Peng, C. (2018). Overview of MicroRNA Biogenesis, Mechanisms of Actions, and Circulation. Frontiers in Endocrinology. 9. 1-12. Available at: … Continue reading It was found that EGCG treatment up-regulated a number of miRNAs involved in cell growth and survival and cell cycle regulation. Some of these included:
EGCG treatment also led to the down-regulation of specific miRNAs involved in the suppression of the cell cycle and induction of apoptosis. Some of these include:
So, to summarize, EGCG can confer some protective effects against cell death, levels of ROS, and subsequent number of senescent cells in DHT-treated cells, indicating that EGCG treatment might be able to negate some effects of DHT in human dermal papilla cells. These effects however were only partial and did not restore levels to the control. Furthermore, it was found that one way that EGCG exerted its effects was by regulating the expression of specific miRNAs involved in cell growth and survival to offset some of the effects of DHT.
Another study was conducted to measure the effect of a range of EGCG concentrations alone on human dermal papilla cells, and a 10% topical treatment on 3 human volunteers (we will go more into this part below).[15]Kwon, O.S., Han, J.H., Yoo, H.G., Chung, J.H., Cho, K.H., Eun, H.C., Kim, K.H. (2007). Human hair growth enhancement in vitro by green tea epigallocatechin-3-gallate (EGCG). Phytomedicine. 14. … Continue reading The effect of EGCG treatment on phosphorylated Erk and Akt expression was then determined using western blot.
The P13-Akt pathway leads to the phosphorylation of the protein P-Akt which promotes keratinocyte survival and growth.[16]Bourguignon, L.Y.W., Matrix hyaluronan-activated CD44 signaling promotes keratinocyte activities and improves abnormal epidermal functions. The American Journal of Pathology. 184(7). 1912-1919. … Continue reading Erk is a protein that when phosphorylates regulates six fundamental processes including cell proliferation, cell survival, cell growth, cell metabolism, cell migration, and cell differentiation.[17]Lavoie, H., Gagnon, J., Therrien, M. (2020). ERK signaling: a master regulator of cell behavior, life, and fate. Nature Reviews Molecular Cell Biology. 21. 607-632. Available at: … Continue reading
Human dermal papilla cells showed a dose-dependent increase in both Erk and Akt protein expression alongside a subsequent increase in cell growth (Figure 6), indicating that EGCG can enhance cell proliferation of human dermal papilla cells.
The researchers also examined the effect of EGCG on key proteins involved in the induction and suppression of apoptosis. Bax is an apoptosis promotor and Bcl-2 is an apoptosis inhibitor.[19]Muller-Rover, S., Rossiter, H., Lindner, G., Peters, E.M.J., Kupper, T.S., Paus, R. (1999). Hair follicle apoptosis and Bcl-2. Journal of Investigative Dermatology. 4. 272-277. Available at: … Continue reading Compared to the control group, EGCG treatment increased protein expression of Bcl-2 – the apoptosis inhibitor – and decreased expression of Bax – the apoptosis promoter – in a dose-dependent manner (Figure 7).
So the in vitro (in cells) data suggests that EGCG can promote hair follicle growth through inhibition of proteins involved in cell death, and the enhancement of expression of proteins involved in cell survival and proliferation. Furthermore, there is also some evidence that EGCG can inhibit 5α-reductase and protect against the effects of DHT.
We can see how EGCG might affect hair follicles, but is there any clinical evidence to show that it works?
The only clinical data that we could find that used EGCG alone – in humans – was a small study conducted on three healthy volunteers who did not have any hair loss disorders.[21]Kwon, O.S., Han, J.H., Yoo, H.G., Chung, J.H., Cho, K.H., Eun, H.C., Kim, K.H. (2007). Human hair growth enhancement in vitro by green tea epigallocatechin-3-gallate (EGCG). Phytomedicine. 14. … Continue reading Ten percent EGCG in ethanol or ethanol vehicle (control) was applied once daily to two areas of the scalp for 4 successive days. The treated areas were then excised and dissected to separate the dermal papillae. These were then lysed and used in a technique called western blotting to determine the protein expression of key markers involved in cell growth Akt and Erk, as well as markers involved in the induction or suppression of apoptosis.
When analyzing the effects of topical EGCG on the expression of the above proteins, it was found that phosphorylated ERK and phosphorylated Akt were both increased, indicating that EGCG confers a positive effect on cell growth (Figure 9). Furthermore, EGCG treatment increased the expression of Bcl-2, a suppressor of apoptosis, and reduced the expression of Bax, a key inducer of apoptosis.
So, these findings indicate that topical EGCG can suppress cell death whilst simultaneously enhancing cell growth in humans. However, this study was not completed in people with any type of hair loss disorder, therefore we cannot say whether it will actually work to stimulate hair growth in those with hair loss.
The European Food Safety Authority has assessed the safety of green tea catechins. They have determined that catechins from green tea infusions and similar drinks are generally safe. However, when taken as a food supplement, catechin doses at or above 800 mg/day may pose health concerns due to liver damage.[23]Younes, M., Aggett, P., Aguilar, F., Crebelli, R., Dusemund, B., Filipic, M., Frutos, M.J., Galtier, P., Gott, D., Gundert-Remy, U., Lambre, C., Leblanc, J.C., Lillegaard, I.T., Moldeus, P., … Continue reading
Based on the limited available data, people with androgenetic alopecia may benefit from EGCG treatment. However, there are no clinical studies undertaken using EGCG alone in patients with hair loss disorders, so we cannot recommend using it alone.
References[+]
↑1 | Singh, B.N., Shankar, S., Srivastava, R.K. (2011). Green tea catechin, epigallocatechin-3-gallate (EGCG): mechanisms, perspectives and clinical applications. Biochemical Pharmacology. 82(12). 1807-1821. Available at: https://doi.org/10.1016/j.bcp.2011.07.093 |
---|---|
↑2 | Dhariwala, M, Y., Ravikumar, P. (2019). An overview of herbal alternatives in androgenetic alopecia. Journal of Cosmetic Dermatology. 18. 966-975. Available at: https://doi.org/10.1111/jocd.12930 |
↑3 | Musial, C., Kuban-Jankowska, A., Gorska, Ponikowska, M. (2020). Beneficial properties of green tea catechins. International Journal of Molecular Science. 21(5). 1744. Available at: https://doi.org/10.3390/ijms21051744 |
↑4, ↑5 | Hiipakka, R.A., Zhang, H.Z., Dai, W., Dai, Q., Liao, S. (2002). Structure-activity relationships for inhibition of human 5α-reductases by polyphenols. Biochemical Pharmacology. 63. 1165-1176. Available at: https://10.1016/s006-2952(02)00848-1 |
↑6, ↑8, ↑9, ↑10 | Shin, S., Kim, K., Lee, M.J., Lee, J., Choi, S., Kim, K.S., Ko, J.M., Han, H., Kim, S.Y., Youn, H.J., Ahn, K.Y., An, I.S., An, S., Cha, H.J. (2016). Epigallocatechin gallate-mediated alteration of the microRNA expression profile in 5α-Dihydrotestosterone-treated human dermal papilla cells. Annals of Dermatology. 28(3). 327-334. Available at: https://10.5021/ad.2016.28.3.327 |
↑7 | Morgan, B.A., (2014). The dermal papilla: an instructive niche for epithelial stem and progenitor cells in development and regeneration of the hair follicle. Cold Spring Harbor Perspectives in Medicine. 4(7). a015180. Available at: https://doi/org/10.1101/cshperspect.a015180 |
↑11 | Lai, J.J., Chang, P., Lai, K.P., Chen, L., Chang, C. (2012). The role of androgen and androgen receptors in skin-related disorders. Archives of Dermatological Research. 304(7). 499-510. Available at: https://doi.org/10.1007/s00403-012-1265-x |
↑12 | Hernandez-Segura, A., Nehme, J., Demaria, M. (2018). Hallmarks of cellular senescence. Trends in Cellular Biology. 28(6). 436-453. Available at: https://doi.org/10.1016/j.tcb.2018.02.001 |
↑13, ↑15, ↑18, ↑21 | Kwon, O.S., Han, J.H., Yoo, H.G., Chung, J.H., Cho, K.H., Eun, H.C., Kim, K.H. (2007). Human hair growth enhancement in vitro by green tea epigallocatechin-3-gallate (EGCG). Phytomedicine. 14. 551-555. Available at: https://doi.org/10.1016/j.phymed.2006.09.009 |
↑14 | O’Brian, J., Hayder, H., Zayed, Y., Peng, C. (2018). Overview of MicroRNA Biogenesis, Mechanisms of Actions, and Circulation. Frontiers in Endocrinology. 9. 1-12. Available at: https://doi.org/10.3389/fendo.2018.00402 |
↑16 | Bourguignon, L.Y.W., Matrix hyaluronan-activated CD44 signaling promotes keratinocyte activities and improves abnormal epidermal functions. The American Journal of Pathology. 184(7). 1912-1919. Available at: https://dx.doi.org/10.1016/j.ajpath.2014.03.010 |
↑17 | Lavoie, H., Gagnon, J., Therrien, M. (2020). ERK signaling: a master regulator of cell behavior, life, and fate. Nature Reviews Molecular Cell Biology. 21. 607-632. Available at: https://doi.org/10.1038/s41580-020-0255-7 |
↑19, ↑20, ↑22 | Muller-Rover, S., Rossiter, H., Lindner, G., Peters, E.M.J., Kupper, T.S., Paus, R. (1999). Hair follicle apoptosis and Bcl-2. Journal of Investigative Dermatology. 4. 272-277. Available at: https://doi.org/10.1038/sj.jidsp.5640228 |
↑23 | Younes, M., Aggett, P., Aguilar, F., Crebelli, R., Dusemund, B., Filipic, M., Frutos, M.J., Galtier, P., Gott, D., Gundert-Remy, U., Lambre, C., Leblanc, J.C., Lillegaard, I.T., Moldeus, P., Mortenson, A., Oskarsson, A., Stankovic, I., Waalkens-Berendsen, I., Wouterson, R.A., Andrade, R.J., Fortes, C., Mosesso, P., Restani, P., Arcella, D., Pizzo, F., Smeraldi, C., Wright. (2018). Scientific opinion on the safety of green tea catechins. EFSA Journal. Available at: https://doi.org/10.2903/j.efsa.2018.5239 |
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Learn MoreDr. Sarah King is a researcher & writer who holds a BSc in Medical Biology, an MSc in Forensic Biology, and a Ph.D. in Molecular and Cellular Biology. While at university, Dr. King’s research focused on cellular aging and senescence through NAD-dependent signaling – along with research into prostaglandins and their role in hair loss. She is a co-author on several upcoming manuscripts with the Perfect Hair Health team.
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