Abstract
Acne vulgaris is the most common skin condition associated with inflammation of pilosebaceous unit. Since conventional therapies have not demonstrated desirable effectiveness and possess remarkable side effects, there is a growing interest in the use of herbal medicines for the management of acne vulgaris. In this study, plant-derived molecules investigated in acne vulgaris have been reviewed and their possible underlying mechanisms of action were discussed. For this purpose, different electronic databases including PubMed, Scopus, Cochrane library and Google Scholar were searched to obtain any in vitro, in vivo, or human studies evaluating the phytochemicals in the management of acne vulgaris. Data were collected from 1980 to 2018 (up to October). Most of the phytochemicals investigated in acne were from the category of polyphenols including resveratrol, myricitrin, schisandrin, terchebulin, alpha-mangotin, curcumin, ellagic acid and epigallocatechin 3-gallate. Moreover, alkaloids and terpenoids such as berberine, ursolic acid, lupeol were evaluated in acne vulgaris with less abundance. Various molecular mechanisms were involved in effects of phytochemicals including antioxidant (through down-regulation of H2O2, MDA, ROS and upregulation of SOD), anti-inflammatory (through reduction of proinflammatory cytokines, i.e., IL-1ß, IL-6, IL-8, TGF-β, TNF-α, NF-κB), immunomodulatory, antibacterial (against Propionibacterium acnes and Propionibacterium granulosum), antiandrogenic, reducing sebum production, and lipogenesis inhibitory activities. Therefore, phytochemicals seem to be a precious source for identifying new medicines for treatment of acne vulgaris; however, since most of studies are preclinical, further clinical studies are needed to achieve more conclusive and reliable results.
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Song YH, Cai H, Gu N et al (2011) Icariin attenuates cardiac remodelling through down-regulating myocardial apoptosis and matrix metalloproteinase activity in rats with congestive heart failure. J Pharm Pharmacol 63(4):541–549
Liu CH, Huang HY (2013) In vitro anti-propionibacterium activity by curcumin containing vesicle system. Chem Pharm Bull (Tokyo) 61(4):419–425
Zouboulis C, Eady A, Philpott M et al (2005) What is the pathogenesis of acne? Exp Dermatol 14(2):143
Wu T-Q, Mei S-Q, Zhang J-X et al (2007) Prevalence and risk factors of facial acne vulgaris among Chinese adolescents. Int J Adolesc Med Health 19(4):407–412
Perkins AC, Maglione J, Hillebrand GG, Miyamoto K, Kimball AB (2012) Acne vulgaris in women: prevalence across the life span. J Womens Health 21(2):223–230
Zaenglein AL, Pathy AL, Schlosser BJ et al (2016) Guidelines of care for the management of acne vulgaris. J Am Acad Dermatol 74(5):945–73.e33
Bhate K, Williams H (2013) Epidemiology of acne vulgaris. Br J Dermatol 168(3):474–485
Rapp SR, Feldman SR, Graham G et al (2006) The acne quality of life index (Acne-QOLI). Am J Clin Dermatol 7(3):185–192
Kapoor S, Saraf S (2011) Topical herbal therapies an alternative and complementary choice to combat acne. Res J Med Plant 5(6):650–659
Tahir I, Khan MR, Shah NA, Aftab M (2016) Evaluation of phytochemicals, antioxidant activity and amelioration of pulmonary fibrosis with Phyllanthus emblica leaves. BMC Complement Altern Med 16(1):406
Williams HC, Dellavalle RP, Garner S (2012) Acne vulgaris. Lancet 379(9813):361–372
Hosein Farzaei M, Bahramsoltani R, Rahimi (2016) Phytochemicals as adjunctive with conventional anticancer therapies. Curr Pharm Des 22(27):4201–4218
Bahramsoltani R, Farzaei MH, Rahimi (2014) Medicinal plants and their natural components as future drugs for the treatment of burn wounds: an integrative review. Arch Dermatol Res 306(7):601–617
Azimi H, Fallah-Tafti M, Khakshur AA, Abdollahi M (2012) A review of phytotherapy of acne vulgaris: perspective of new pharmacological treatments. Fitoterapia 83(8):1306–1317
Nishijima S, Kurokawa I, Katoh N, Watanabe K (2000) The bacteriology of acne vulgaris and antimicrobial susceptibility of Propionibacterium acnes and Staphylococcus epidermidis isolated from acne lesions. J Dermatol 27(5):318–323
Gollnick H (2003) Current concepts of the pathogenesis of acne. Drugs 63(15):1579–1596
Ganceviciene R, Fimmel S, Glass E, Zouboulis CC (2006) Psoriasin and follicular hyperkeratinization in acne comedones. Dermatology 213(3):270–272
Degitz K, Placzek M, Borelli C, Plewig G (2007) Pathophysiology of acne. J Dtsch Dermatol Ges 5(4):316–323
Vora J, Srivastava A, Modi H (2017) Antibacterial and antioxidant strategies for acne treatment through plant extracts. Inf Med Unlock 13:128–132
Kim J, Ochoa M-T, Krutzik SR et al (2002) Activation of toll-like receptor 2 in acne triggers inflammatory cytokine responses. J Immunol 169(3):1535–1541
Jeremy AH, Holland DB, Roberts SG, Thomson KF, Cunliffe WJ (2003) Inflammatory events are involved in acne lesion initiation. J Invest Dermatol 121(1):20–27
Tanghetti EA (2013) The role of inflammation in the pathology of acne. J Clin Aesthet Dermatol 6(9):27
Downie MM, Kealey T (1998) Lipogenesis in the human sebaceous gland: glycogen and glycerophosphate are substrates for the synthesis of sebum lipids. J Invest Dermatol 111(2):199–205
McNairn AJ, Doucet Y, Demaude J et al (2013) TGFβ signaling regulates lipogenesis in human sebaceous glands cells. BMC Dermatol 13(1):2
Lyon CC (2001) Acne: diagnosis and management. SAGE Publications Sage UK, London
Arican O, Kurutas EB, Sasmaz S (2005) Oxidative stress in patients with acne vulgaris. Mediators Inflamm 2005(6):380–384
Jung H-A, Su B-N, Keller WJ, Mehta RG, Kinghorn AD (2006) Antioxidant xanthones from the pericarp of Garcinia mangostana (Mangosteen). J Agric Food Chem 54(6):2077–2082
Asasutjarit R, Larpmahawong P, Fuongfuchat A, Sareedenchai V, Veeranondha S (2014) Physicochemical properties and anti-Propionibacterium acnes activity of film-forming solutions containing alpha-mangostin-rich extract. AAPS Pharm Sci Tech 15(2):306–316
Zou W, Yin P, Shi Y et al (2019) A novel biological role of α-Mangostin via TAK1-NF-κB pathway against inflammatory. Inflammation 42(1):103–112
Franceschelli S, Pesce M, Ferrone A et al (2016) A novel biological role of alpha-mangostin in modulating inflammatory response through the activation of SIRT-1 signaling pathway. J Cell Physiol 231(11):2439–2451
Fang Y, Su T, Qiu X et al (2016) Protective effect of alpha-mangostin against oxidative stress induced-retinal cell death. Sci Rep 6:1018–1038
Marquez-Valadez B, Maldonado PD, Galvan-Arzate S et al (2012) Alpha-mangostin induces changes in glutathione levels associated with glutathione peroxidase activity in rat brain synaptosomes. Nutr Neurosci 15(5):13–19
Kou X, Chen N (2012) Pharmacological potential of ampelopsin in Rattan tea. Food Sci Hum Wellness 1(1):14–18
Qi S, Xin Y, Guo Y et al (2012) Ampelopsin reduces endotoxic inflammation via repressing ROS-mediated activation of PI3K/Akt/NF-κB signaling pathways. Int Immunopharmacol 12(1):278–287
Weng L, Zhang H, Li X et al (2017) Ampelopsin attenuates lipopolysaccharide-induced inflammatory response through the inhibition of the NF-κB and JAK2/STAT3 signaling pathways in microglia. Int Immunopharmacol 44:1–8
Hou X, Zhang J, Ahmad H et al (2014) Evaluation of antioxidant activities of ampelopsin and its protective effect in lipopolysaccharide-induced oxidative stress piglets. PLoS ONE 9(9):e108314
Farzaei MH, Rahimi R, Abdollahi M (2015) The role of dietary polyphenols in the management of inflammatory bowel disease. Curr Pharm Biotechnol 16(3):196–210
Lee KE, Youm JK, Lee WJ, Kang S, Kim YJ (2017) Polyphenol-rich apple extract inhibits dexamethasone-induced sebaceous lipids production by regulating SREBP1 expression. Exp Dermatol 26(10):958–960
Lu Y, Foo LY (2000) Antioxidant and radical scavenging activities of polyphenols from apple pomace. Food Chem 68(1):81–85
Skyberg JA, Robison A, Golden S et al (2011) Apple polyphenols require T cells to ameliorate dextran sulfate sodium-induced colitis and dampen proinflammatory cytokine expression. J Leukoc Biol 90(6):1043–1054
Xu ZR, Li JY, Dong XW et al (2015) Apple polyphenols decrease atherosclerosis and hepatic steatosis in ApoE−/− mice through the ROS/MAPK/NF-kappaB pathway. Nutrients 7(8):7085–7105
Etti IC, Abdullah R, Kadir A et al (2017) The molecular mechanism of the anticancer effect of Artonin E in MDA-MB 231 triple negative breast cancer cells. PLoS ONE 12(8):e0182357
Nayak M, Nagarajan A, Majeed M, Nagabhushanam K, Choudhury AK (2017) In vitro anti-acne activity of phytoactives from the stem bark of Artocarpus hirsutus Lam. and characterisation of pyranocycloartobiloxanthone A as a mixture of two anomers. Nat Prod Res 2017:1–5
Reddy GR, Ueda N, Hada T et al (1991) A prenylflavone, artonin E, as arachidonate 5-lipoxygenase inhibitor. Biochem Pharmacol 41(1):115–118
Li CG, Yan L, Jing YY et al (2017) Berberine augments ATP-induced inflammasome activation in macrophages by enhancing AMPK signaling. Oncotarget 8(1):95–109
Spatuzza C, Postiglione L, Covelli B et al (2014) Effects of berberine and red yeast on proinflammatory cytokines IL-6 and TNF-alpha in peripheral blood mononuclear cells (PBMCs) of human subjects. Front pharmacol 5:230
Zhang H, Shan Y, Wu Y et al (2017) Berberine suppresses LPS-induced inflammation through modulating Sirt1/NF-kappaB signaling pathway in RAW264.7 cells. Int Immunopharmacol 52:93–100
Sun Y, Yuan X, Zhang F et al (2017) Berberine ameliorates fatty acid-induced oxidative stress in human hepatoma cells. Sci Rep 7(1):11340
Sadeghnia HR, Kolangikhah M, Asadpour E, Forouzanfar F, Hosseinzadeh H (2017) Berberine protects against glutamate-induced oxidative stress and apoptosis in PC12 and N2a cells. Iran J Basic Med Sci 20(5):594–603
Tian Y, Zhao L, Wang Y et al (2016) Berberine inhibits androgen synthesis by interaction with aldo-keto reductase 1C3 in 22Rv1 prostate cancer cells. Asian J Androl 18(4):607–612
Seki T, Morohashi M (1993) Effect of some alkaloids, flavonoids and triterpenoids, contents of Japanese–Chinese traditional herbal medicines, on the lipogenesis of sebaceous glands. Skin Pharmacol Physiol 6(1):56–60
Farzaei MH, Zobeiri M, Parvizi F et al (2018) Curcumin in liver diseases: a systematic review of the cellular mechanisms of oxidative stress and clinical perspective. Nutrients 10:7
Haghi A, Azimi H, Rahimi R (2017) A comprehensive review on pharmacotherapeutics of three phytochemicals, curcumin, quercetin, and Allicin, in the treatment of gastric cancer. J Gastrointest Cancer 48(4):314–320
Liu CH, Huang HY (2012) Antimicrobial activity of curcumin-loaded myristic acid microemulsions against Staphylococcus epidermidis. Chem Pharm Bull 60(9):1118–1124
Dai J, Gu L, Su Y et al (2018) Inhibition of curcumin on influenza A virus infection and influenzal pneumonia via oxidative stress, TLR2/4, p38/JNK MAPK and NF-kappaB pathways. Int Immunopharmacol 54:177–187
Zhang Z, Li K (2018) Curcumin attenuates high glucose-induced inflammatory injury through the reactive oxygen species-phosphoinositide 3-kinase/protein kinase B-nuclear factor-kappaB signaling pathway in rat thoracic aorta endothelial cells. J Diabetes Investig 9(4):731–740
Yu S, Wang M, Guo X, Qin R (2018) Curcumin attenuates inflammation in a severe acute pancreatitis animal model by regulating TRAF1/ASK1 signaling. Med Sci Monit 24:2280–2286
Sivasankar C, Maruthupandiyan S, Balamurugan K et al (2016) A combination of ellagic acid and tetracycline inhibits biofilm formation and the associated virulence of Propionibacterium acnes in vitro and in vivo. Biofouling 32(4):397–410
Umesalma S, Sudhandiran G (2010) Differential inhibitory effects of the polyphenol ellagic acid on inflammatory mediators NF-κB, iNOS, COX-2, TNF-α, and IL-6 in 1, 2-dimethylhydrazine-induced rat colon carcinogenesis. Basic Clin Pharmacol Toxicol 107(2):650–655
Rios JL, Giner RM, Marin M, Recio MC (2018) A pharmacological update of ellagic acid. Planta Med
Rozentsvit A, Vinokur K, Samuel S, Li Y, Gerdes AM, Carrillo-Sepulveda MA (2017) Ellagic acid reduces high glucose-induced vascular oxidative stress through ERK1/2/NOX4 signaling pathway. Cell Physiol Biochem 44(3):1174–1187
Ural MS, Yonar ME, Mise Yonar S (2015) Protective effect of ellagic acid on oxidative stress and antioxidant status in Cyprinus carpio during malathion exposure. Cell Mol Biol (Noisy-le-grand) 61(5):58–63
Uzar E, Alp H, Cevik MU et al (2012) Ellagic acid attenuates oxidative stress on brain and sciatic nerve and improves histopathology of brain in streptozotocin-induced diabetic rats. Neurol Sci 33(3):567–574
Farzaei MH, Shahpiri Z, Bahramsoltani R et al (2017) Efficacy and tolerability of phytomedicines in multiple sclerosis patients: a review. CNS Drugs 31(10):867–889
Yoon JY, Kwon HH, Min SU, Thiboutot DM, Suh DH (2013) Epigallocatechin-3-gallate improves acne in humans by modulating intracellular molecular targets and inhibiting P. acnes. J Invest Dermatol 133(2):429–440
Koseki J, Matsumoto T, Matsubara Y et al (2015) Inhibition of Rat 5alpha-reductase activity and testosterone-induced sebum synthesis in hamster sebocytes by an extract of quercus acutissima cortex. Evid Based Complement Alternat Med. 2015:853846
Yang N, Zhang H, Cai X, Shang Y (2018) Epigallocatechin-3-gallate inhibits inflammation and epithelialmesenchymal transition through the PI3K/AKT pathway via upregulation of PTEN in asthma. Int J Mol Med 41(2):818–828
Shi J, Deng H, Pan H, Xu Y, Zhang M (2017) Epigallocatechin-3-gallate attenuates microcystin-LR induced oxidative stress and inflammation in human umbilical vein endothelial cells. Chemosphere 168:25–31
Guo M, An F, Wei X, Hong M, Lu Y (2017) Comparative effects of schisandrin A, B, and C on acne-related inflammation. Inflammation 40(6):2163–2172
Batubara I, Kuspradini H, Muddathir AM, Mitsunaga T (2014) Intsia palembanica wood extracts and its isolated compounds as Propionibacterium acnes lipase inhibitor. J Wood Sci 60(2):169–174
Moon JE, Shin J-H, Kwon O, Kim JY, Jomf J (2015) A standardized extract of rhus verniciflua stokes protects wistar rats against lipopolysaccharide-induced acute inflammation. J Med Food 18(11):1223–1230
Kahkeshani N, Farzaei F, Fotouhi M et al (2019) Pharmacological effects of gallic acid in health and disease: a mechanistic review. Iran J Basic Med Sci 22(3):225–237
Lin WH, Kuo HH, Ho LH, Tseng ML, Siao AC, Hung CT et al (2015) Gardenia jasminoides extracts and gallic acid inhibit lipopolysaccharide-induced inflammation by suppression of JNK2/1 signaling pathways in BV-2 cells. Iran J Basic Med Sci 18(6):555–562
Wei G, Wu Y, Gao Q et al (2018) Gallic acid attenuates postoperative intra-abdominal adhesion by inhibiting inflammatory reaction in a rat model. Med Sci Monit 24:827–838
Oyagbemi AA, Omobowale TO, Saba AB et al (2016) Gallic acid ameliorates cyclophosphamide-induced neurotoxicity in Wistar rats through free radical scavenging activity and improvement in antioxidant defense system. J Diet Suppl 13(4):402–419
Mohamed HM, Abd El-Twab SM (2016) Gallic acid attenuates chromium-induced thyroid dysfunction by modulating antioxidant status and inflammatory cytokines. Environ Toxicol Pharmacol 48:225–236
Tsai PJ, Huang WC, Hsieh MC et al (2015) Flavones isolated from scutellariae radix suppress propionibacterium acnes-induced cytokine production in vitro and in vivo. Molecules 21(1):E15
Lim BO, Yu BP, Kim SC, Park DK (1999) The antioxidative effect of ganhuangenin against lipid peroxidation. Phytother Res 13(6):479–483
Nian H, Ma M-H, Nian S-S, Xu L-L (2009) Antiosteoporotic activity of icariin in ovariectomized rats. Phytomedicine 16(4):320–326
Xu CQ, Liu BJ, Wu JF et al (2010) Icariin attenuates LPS-induced acute inflammatory responses: involvement of PI3K/Akt and NF-kappaB signaling pathway. Eur J Pharmacol 642(1–3):146–153
Kong L, Liu J, Wang J, Luo Q, Zhang H, Liu B et al (2015) Icariin inhibits TNF-alpha/IFN-gamma induced inflammatory response via inhibition of the substance P and p38-MAPK signaling pathway in human keratinocytes. Int Immunopharmacol 29(2):401–407
Song YH, Cai H, Zhao ZM et al (2016) Icariin attenuated oxidative stress induced-cardiac apoptosis by mitochondria protection and ERK activation. Biomed Pharmacother 83:1089–1094
Li WW, Gao XM, Wang XM, Guo H, Zhang BL (2011) Icariin inhibits hydrogen peroxide-induced toxicity through inhibition of phosphorylation of JNK/p38 MAPK and p53 activity. Mutat Res 708(1–2):1–10
Demetzos C, Dimas KS (2001) Labdane-type diterpenes: chemistry and biological activity. Stud Nat Prod Chem 25:235–292
Girón N, Través PG, Rodríguez B et al (2008) Supression of inflammatory responses by labdane-type diterpenoids. Toxicol Appl Pharmacol 228(2):179–189
Van Kiem P, Anh HLT, Nhiem NX et al (2012) Labdane-type diterpenoids from the rhizomes of Hedychium coronarium inhibit lipopolysaccharide-stimulated production of pro-inflammatory cytokines in bone marrow-derived dendritic cells. Chem Pharm Bull (Tokyo) 60(2):246–250
Liu F, He Y, Liang Y et al (2013) PI3-kinase inhibition synergistically promoted the anti-tumor effect of lupeol in Hepatocellular carcinoma. Cancer Cell Int 13(1):108
Kwon HH, Yoon JY, Park SY, Min S, Kim YI, Park JY et al (2015) Activity-guided purification identifies lupeol, a pentacyclic triterpene, as a therapeutic agent targeting multiple pathogenic factors of acne. Invest Dermatol 135(6):1491–1500
Zhu Y, Li X, Chen J, Chen T, Shi Z, Lei M et al (2016) The pentacyclic triterpene Lupeol switches M1 macrophages to M2 and ameliorates experimental inflammatory bowel disease. Int Immunopharmacol 30:74–84
Prasad S, Kalra N, Singh M, Shukla Y (2008) Protective effects of lupeol and mango extract against androgen induced oxidative stress in Swiss albino mice. Asian J Androl 10(2):313–318
Semwal DK, Semwal RB, Combrinck S, Viljoen A (2016) Myricetin: a dietary molecule with diverse biological activities. Nutrients 8(2):90
Hou W, Hu S, Su Z et al (2018) Myricetin attenuates LPS-induced inflammation in RAW 264.7 macrophages and mouse models. Future Med Chem 10(19):2253–2264
da Lee H, Lee CS (2016) Flavonoid myricetin inhibits TNF-alpha-stimulated production of inflammatory mediators by suppressing the Akt, mTOR and NF-kappaB pathways in human keratinocytes. Eur J Pharmacol 784:164–172
Cho BO, Yin HH, Park SH et al (2016) Anti-inflammatory activity of myricetin from Diospyros lotus through suppression of NF-kappaB and STAT1 activation and Nrf2-mediated HO-1 induction in lipopolysaccharide-stimulated RAW264.7 macrophages. Biosci Biotechnol Biochem 80(8):1520–1530
Kang KA, Wang ZH, Zhang R et al (2010) Myricetin protects cells against oxidative stress-induced apoptosis via regulation of PI3K/Akt and MAPK signaling pathways. Int J Mol Sci 11(11):4348–4360
Chobot V, Hadacek F (2011) Exploration of pro-oxidant and antioxidant activities of the flavonoid myricetin. Redox Rep 16(6):242–247
Pereira M, Siba I, Chioca L et al (2011) Myricitrin, a nitric oxide and protein kinase C inhibitor, exerts antipsychotic-like effects in animal models. Prog Neuropsychopharmacol Biol Psychiatry 35(7):1636–1644
Qi S, Feng Z, Li Q, Qi Z, Zhang Y (2017) Myricitrin modulates NADPH oxidase-dependent ROS production to inhibit endotoxin-mediated inflammation by blocking the JAK/STAT1 and NOX2/p47(phox) pathways. Oxid Med Cell Longev 2017:9738745
Gao J, Chen S, Qiu Z et al (2018) Myricitrin ameliorates ethanol-induced steatosis in mouse AML12 liver cells by activating AMPK, and reducing oxidative stress and expression of inflammatory cytokines. Mol Med Rep 17(5):7381–7387
Domitrovic R, Rashed K, Cvijanovic O, Vladimir-Knezevic S, Skoda M, Visnic A (2015) Myricitrin exhibits antioxidant, anti-inflammatory and antifibrotic activity in carbon tetrachloride-intoxicated mice. Chem Biol Interact 230:21–29
Sun GB, Qin M, Ye JX et al (2013) Inhibitory effects of myricitrin on oxidative stress-induced endothelial damage and early atherosclerosis in ApoE−/− mice. Toxicol Appl Pharmacol 271(1):114–126
Jung MK, Ha S, Son JA et al (2012) Polyphenon-60 displays a therapeutic effect on acne by suppression of TLR2 and IL-8 expression via down-regulating the ERK1/2 pathway. Arch Dermatol Res 304(8):655–663
Sidahmed HM, Hashim NM, Amir J et al (2013) Pyranocycloartobiloxanthone A, a novel gastroprotective compound from Artocarpus obtusus Jarret, against ethanol-induced acute gastric ulcer in vivo. Phytomedicine 20(10):834–843
Hashim NM, Rahmani M, Ee GCL et al (2012) Antioxidant, antimicrobial and tyrosinase inhibitory activities of xanthones isolated from Artocarpus obtusus FM Jarrett. Molecules 17(5):6071–6082
Farzaei MH, Rahimi R, Nikfar S, Abdollahi M (2018) Effect of resveratrol on cognitive and memory performance and mood: a meta-analysis of 225 patients. Pharmacol Res 128:338–344
Taylor EJ, Yu Y, Champer J, Kim J (2014) Resveratrol demonstrates antimicrobial effects against propionibacterium acnes in vitro. Dermatol Ther (Heidelb) 4(2):249–257
Docherty JJ, McEwen HA, Sweet TJ, Bailey E, Booth TD (2007) Resveratrol inhibition of Propionibacterium acnes. J Antimicrob Chemother 59(6):1182–1184
Leejae S, Hasap L, Voravuthikunchai SP (2013) Inhibition of staphyloxanthin biosynthesis in Staphylococcus aureus by rhodomyrtone, a novel antibiotic candidate. J Med Microbiol 62(Pt 3):421–428
Chorachoo J, Amnuaikit T, Voravuthikunchai SP (2013) Liposomal encapsulated rhodomyrtone: a novel antiacne drug. Evid Based Complement Alternat Med 2013:157635
Saising J, Ongsakul M, Voravuthikunchai SP (2011) Rhodomyrtus tomentosa (Aiton) Hassk. ethanol extract and rhodomyrtone: a potential strategy for the treatment of biofilm-forming staphylococci. J Med Microbiol 60(12):1793–1800
Park SY, Kim YH, Kim Y et al (2011) Upregulation of heme oxygenase-1 via PI3K/Akt and Nrf-2 signaling pathways mediates the anti-inflammatory activity of Schisandrin in Porphyromonas gingivalis LPS-stimulated macrophages. Immunol Lett 139:93–101
Cai Z, Liu J, Bian H, Cai J, Zhu G (2016) Suppression of P2X7/NF-κB pathways by Schisandrin B contributes to attenuation of lipopolysaccharide-induced inflammatory responses in acute lung injury. Arch Pharm Res 39(4):499–507
Ran J, Ma C, Xu K, et al (2018) Schisandrin B ameliorated chondrocytes inflammation and osteoarthritis via suppression of NF-kappaB and MAPK signal pathways. Drug Des Devel Ther 12:1195–1204
Takanche JS, Lee YH, Kim JS et al (2018) Anti-inflammatory and antioxidant properties of Schisandrin C promote mitochondrial biogenesis in human dental pulp cells. Int Endod J 51(4):438–447
Kwon DH, Cha HJ, Choi EO, Leem SH, Kim GY, Moon SK et al (2018) Schisandrin A suppresses lipopolysaccharide-induced inflammation and oxidative stress in RAW 264.7 macrophages by suppressing the NF-kappaB, MAPKs and PI3K/Akt pathways and activating Nrf2/HO-1 signaling. Int J Mol Med 41(1):264–74
Ying W, Li ZC, Li-Qing Y, Mai L, Mei T (2018) Schisandrin B alleviates acute oxidative stress via modulating Nrf2/Keap1-mediated antioxidant pathway. Appl Physiol Nutr Metab 2018:1–24.
Muddathir AM, Yamauchi K, Mitsunaga T (2013) Anti-acne activity of tannin-related compounds isolated from Terminalia laxiflora. J Wood Sci 59(5):426–431
Sultana N (2011) Clinically useful anticancer, antitumor, and antiwrinkle agent, ursolic acid and related derivatives as medicinally important natural product. J Enzyme Inhib Med Chem 26(5):616–642
Zhang Z, Zhang H, Chen R, Wang Z (2018) Oral supplementation with ursolic acid ameliorates sepsis-induced acute kidney injury in a mouse model by inhibiting oxidative stress and inflammatory responses. Mol Med Rep 17(5):7142–7148
Peng J, Ren X, Lan T et al (2016) Renoprotective effects of ursolic acid on ischemia/reperfusion induced acute kidney injury through oxidative stress, inflammation and the inhibition of STAT3 and NFkappaB activities. Mol Med Rep 14(4):3397–3402
Ma JQ, Ding J, Zhang L, Liu CM (2014) Ursolic acid protects mouse liver against CCl4-induced oxidative stress and inflammation by the MAPK/NF-kappaB pathway. Environ Toxicol Pharmacol 37(3):975–983
Fabbrocini G, Staibano S, De Rosa G et al (2011) Resveratrol-containing gel for the treatment of acne vulgaris: a single-blind, vehicle-controlled, pilot study. Am J Clin Dermatol 12(2):133–141
Pan-In P, Wongsomboon A, Kokpol C, Chaichanawongsaroj N, Wanichwecharungruang S (2015) Depositing alpha-mangostin nanoparticles to sebaceous gland area for acne treatment. J Pharmacol Sci 129(4):226–232
Lee JW, Kang YJ, Choi HK, Yoon YG (2018) Fractionated Coptis chinensis extract and its bioactive component suppress Propionibacterium acnes-stimulated inflammation in human keratinocytes. J Microbiol Biotechnol
Im M, Kim SY, Sohn KC, Choi DK, Lee Y, Seo YJ et al (2012) Epigallocatechin-3-gallate suppresses IGF-I-induced lipogenesis and cytokine expression in SZ95 sebocytes. J Invest Dermatol 132(12):2700–2708
Coenye T, Brackman G, Rigole P, De Witte E, Honraet K, Rossel B et al (2012) Eradication of Propionibacterium acnes biofilms by plant extracts and putative identification of icariin, resveratrol and salidroside as active compounds. Phytomedicine 19(5):409–412
Sultan MZ, Jeon YM, Moon SS (2008) Labdane-type diterpenes active against acne from pine cones (Pinus densiflora). Planta med 74(4):449–452
Sharma R, Kishore N, Hussein A, Lall N (2013) Antibacterial and anti-inflammatory effects of Syzygium jambos L. (Alston) and isolated compounds on acne vulgaris. BMC Complement Altern Med 13:292
Wunnoo S, Saising J, Voravuthikunchai SP (2017) Rhodomyrtone inhibits lipase production, biofilm formation, and disorganizes established biofilm in Propionibacterium acnes. Anaerobe 43:61–68
Saising J, Voravuthikunchai SP (2012) Anti-Propionibacterium acnes activity of rhodomyrtone, an effective compound from Rhodomyrtus tomentosa (Aiton) Hassk. leaves. Anaerobe 18(4):400–404
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Soleymani, S., Farzaei, M.H., Zargaran, A. et al. Promising plant-derived secondary metabolites for treatment of acne vulgaris: a mechanistic review. Arch Dermatol Res 312, 5–23 (2020). https://doi.org/10.1007/s00403-019-01968-z
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DOI: https://doi.org/10.1007/s00403-019-01968-z