2,4,6-Triphenyl-1-hexene, an Anti-Melanogenic Compound from Marine-Derived Bacillus sp. APmarine135

Although melanin protects against ultraviolet radiation, its overproduction causes freckles and senile lentigines. Recently, various biological effects of metabolites derived from marine microorganisms have been highlighted due to their potential for biological and pharmacological applications. In this study, we discovered the anti-melanogenic effect of Bacillus sp. APmarine135 and verified the skin-whitening effect. Fractions of APmarine135 showed the melanin synthesis inhibition effect in B16 melanoma cells, and 2,4,6-triphenyl-1-hexene was identified as an active compound. The melanogenic capacity of 2,4,6-triphenyl-1-hexene (1) was investigated by assessing the intracellular melanin content in B16 cells. Treatment with 5 ppm of 2,4,6-triphenyl-1-hexene (1) for 72 h suppressed the α-melanocyte-stimulating hormone (α-MSH)-induced intracellular melanin increase to the same level as in the untreated control group. Additionally, 2,4,6-triphenyl-1-hexene (1) treatment suppressed the activity of tyrosinase, the rate-limiting enzyme for melanogenesis. Moreover, 2,4,6-triphenyl-1-hexene (1) treatment downregulated tyrosinase, Tyrp-1, and Tyrp-2 expression by inhibiting the microphthalmia-associated transcription factor (MITF). Furthermore, 2,4,6-triphenyl-1-hexene (1) treatment decreased the melanin content in the three-dimensional (3D) human-pigmented epidermis model MelanoDerm and exerted skin-whitening effects. Mechanistically, 2,4,6-triphenyl-1-hexene (1) exerted anti-melanogenic effects by suppressing tyrosinase, Tyrp-1, and Tyrp-2 expression and activities via inhibition of the MITF. Collectively, these findings suggest that 2,4,6-triphenyl-1-hexene (1) is a promising anti-melanogenic agent in the cosmetic industry.


Introduction
Melanogenesis is the process of melanin production to protect the skin against the deleterious effects of ultraviolet (UV) radiation [1].However, melanin overproduction causes freckles, senile lentigines, and other forms of melanin hyperpigmentation, which are serious aesthetic problems [2].Melanogenesis is regulated by three key enzymes: tyrosinase and tyrosinase-related protein (TRP)-1 and -2 [3].Tyrosinase is a rate-limiting enzyme that catalyzes two different steps in melanogenesis: the hydroxylation of L-tyrosine to 3,4-dihydroxyphenylalanine (DOPA) and the subsequent oxidation of DOPA to dopaquinine.TRP-1 catalyzes the oxidation of indol-5,6-quinone 2-carboxylic acid (DHICA) to carboxylated indole-quinone, whereas TRP-2 catalyzes the conversion of DOPA chrome to TRP-2 by binding to their promoter sites [5].Thus, the upregulation or activation melanogenic proteins can increase melanin synthesis, whereas inhibiting these p could be an effective strategy for skin whitening.Several studies have been cond identify and isolate tyrosinase inhibitors from various natural and synthetic sourc ically, these inhibitors are tested using monophenolic substrates such as tyrosin phenolic substrates such as L-dopa, with their effectiveness assessed based pachrome formation.
Although several synthetic anti-melanogenic agents have been reported, the cations as cosmetic ingredients are limited due to severe side effects in humans, high toxicity, low stability, poor skin penetration, and odor [6].Therefore, recent on anti-melanogenic agents have focused on natural products that are free of side Marine microorganisms found in unexplored habitats, such as deep-sea sed hydrothermal vents, and Arctic and Antarctic waters, have the potential to produ metabolites with diverse biological activities [7].Particularly, research evidence in that bacteria, fungi, and cyanobacteria, closely associated with sponges, are real pr of the bioactive compounds isolated from the sponges.For example, 140 novel b compounds have been isolated from microorganisms associated with sponges b 2017 and 2022, indicating that they are a reservoir for natural products [8].In co marine microorganisms have attracted attention due to the presence of novel com with photoprotective, anti-aging, antioxidant, and skin-whitening activities [9].studies have revealed that small molecules from marine bacteria, such as pseud mone A, deoxyvasicinone, (-)-4-hydroxysattabacin, and homothallin-II, exhibit an nogenic effects [10][11][12][13].Additionally, the culture extract of Bacillus sp.APma strongly inhibits melanogenesis in MSH-stimulated B16 melanoma cells.

Anti-Melanogenic Evaluation of APmarine135 Fractions
The Bacillus sp.APmarine135 was cultivated in 2 L of a SYP medium (10 g/L starch, 4 g/L yeast, 2 g/L peptone, and 34.25 g/L sea salt in 1 L distilled water) fo under constant shaking.After 60 h, sterilized a HP-20 resin (200 mL) was adde

Inhibition of Epidermal Pigmentation via 2,4,6-Triphenyl-1-hexene on a 3D Human Skin Equivalent Model
So far, we demonstrated the anti-melanogenic effect and mechanism of 2,4,6-triphenyl-1-hexene in B16 cells.However, skin pigmentation is a complex reaction consisting of melanin synthesis, transport, and transfer.Briefly, melanin produced in melanocytes at the basal layer of the epidermis is transferred to adjacent keratinocytes in the form of melanosomes.Through the sequential differentiation processes of keratinocytes, the transferred melanin is accumulated up to the outermost layer of the epidermis stratum corneum and epidermal pigmentation is completed.On the basis of this, we observed the (A) Cellular tyrosinase activity was spectrophotometrically measured at 475 nm, as described in Materials and Methods.(B) The protein expression of tyrosinase in B16 cells was determined using Western blot analysis.Cells were treated with 2,4,6-triphenyl-1-hexene for 48 h.Equal amounts of proteins were separated using 10% SDS-PAGE and detected using specific antibodies.β-Actin was detected as a loading control.(C,D) mRNA levels of melanogenic protein-encoding genes in B16 cells were determined using real-time qPCR.Cells were treated with 2,4,6-triphenyl-1-hexene for 24 h.The mRNA levels of the genes encoding tyrosinase, Tyrp-1, Tyrp-2, and the MITF were normalized to those of β-actin.The results for B16 cells are presented as means ± standard deviation (SD), expressed as a percentage relative to controls (* p < 0.05, ** p < 0.01, *** p < 0.001 vs. the α-MSH-treated group; ### p < 0.001 vs. the α-MSH-untreated control group).
In the current study, we used α-melanocyte-stimulating hormone (α-MSH)-stimulated B16 murine melanoma cells to find the anti-melanogenic efficacy of 2,4,6-triphenyl-1-hexene (1).α-MSH, known as a family of peptide hormones, stimulates the production and release of melanin via melanocytes in the skin.In B16 melanoma cells, α-MSH activates tyrosinase and melanogenesis via adenyl cyclase activation.Namely, in response to α-MSH, B16 melanoma cells underwent differentiation characterized by increased melanin biosynthesis [17].Therefore, many studies have conducted experiments using B16 cell lines stimulated with α-MSH to verify the inhibition of melanin production via whitening materials [17][18][19][20].In particular, referring to these reports, since α-MSH maximizes melanin production in B16 around 72 h, the inhibitory efficacy of melanin production via 2,4,6triphenyl-1-hexene was also verified at 72 h in α-MSH-stimulated B16 cells in this study.In addition, in order to examine the inhibitory effect of 2,4,6-triphenyl-1-hexene (1) on the potent targets involved in melanin production, the current experiments were performed at 48 h for the protein level and 24 h for the mRNA level.Although the general in vitro experiment using the α-MSH-stimulated B16 cells is widely accepted, it was thought that it would be more realistic to verify the anti-melanogenic efficacy using human melanocytes.However, experimental data using human cells were not obtained in this study.Instead, we obtained more meaningful and realistic whitening efficacy data in this study using a 3D reconstructed skin model.
In the current study, we used α-melanocyte-stimulating hormone (α-MSH)-stimulated B16 murine melanoma cells to find the anti-melanogenic efficacy of 2,4,6-triphenyl-1hexene (1).α-MSH, known as a family of peptide hormones, stimulates the production and release of melanin via melanocytes in the skin.In B16 melanoma cells, α-MSH activates tyrosinase and melanogenesis via adenyl cyclase activation.Namely, in response to α-MSH, B16 melanoma cells underwent differentiation characterized by increased melanin biosynthesis [17].Therefore, many studies have conducted experiments using B16 cell lines stimulated with α-MSH to verify the inhibition of melanin production via whitening materials [17][18][19][20].In particular, referring to these reports, since α-MSH maximizes melanin production in B16 around 72 h, the inhibitory efficacy of melanin production via 2,4,6triphenyl-1-hexene was also verified at 72 h in α-MSH-stimulated B16 cells in this study.In addition, in order to examine the inhibitory effect of 2,4,6-triphenyl-1-hexene (1) on the potent targets involved in melanin production, the current experiments were performed at 48 h for the protein level and 24 h for the mRNA level.Although the general in vitro experiment using the α-MSH-stimulated B16 cells is widely accepted, it was thought that it would be more realistic to verify the anti-melanogenic efficacy using human melanocytes.However, experimental data using human cells were not obtained in this study.Instead, we obtained more meaningful and realistic whitening efficacy data in this study using a 3D reconstructed skin model.
In general, many anti-melanogenic compounds based on tyrosinase inhibition are characterized by having tyrosine moiety.However, despite its anti-melanogenic activity, 2,4,6-triphenyl-1-hexene (1) does not contain any phenolic group derived from tyrosine.To the best of our knowledge, 2,4,6-triphenyl-1-hexene (1) is the first class of anti-melanogenic inhibitors without any tyrosine moiety in its structure.The ability of 2,4,6-triphenyl-1hexne (1) to inhibit melanin production was also confirmed using color photographs of B16 cells.To define the underlying molecular mechanisms of 2,4,6-triphenyl-1-hexene (1) in anti-melanogenesis, we first confirmed that 2,4,6-triphenyl-1-hexene (1) suppressed the activity of tyrosinase, the rate-limiting enzyme for melanogenesis.As shown in Figure 4A, 2,4,6-triphenyl-1-hexene (1) slightly but significantly reduced the activity of tyrosinase.However, because it did not strongly inhibit tyrosinase activity, it was difficult to consider that inhibition of tyrosinase activity via 2,4,6-triphenyl-1-hexene (1) would have played an important role in melanin production.In addition, it was observed that the results of tyrosinase activity inhibition were slightly different depending on whether L-tyrosine and L-DOPA were used as substrates.This may be predicted as a result of the substrate concentration or solvent due to limitations in in vitro experimental conditions, but there is also the possibility that inhibition of tyrosinase activity via 2,4,6-triphenyl-1-hexene (1) may differ depending on the substrate on which tyrosinase acts during the melanin production process.Therefore, we conducted additional experiments focusing on the inhibition of protein expression rather than the efficacy in inhibiting tyrosinase activity via 2,4,6-triphenyl-1-hexene (1).As expected, 2,4,6-triphenyl-1-hexene (1) induced a reduction in tyrosinase, Tyrp-1, and Tyrp-2 expression through the MITF inhibition, confirming that this is the mechanism by which melanin production is suppressed (Figure 4B,C).Interestingly, 2,4,6-triphenyl-1-hexene (1) significantly suppressed both tyrosinase expression and activity.These results imply that 2,4,6-triphenyl-1-hexene (1) could act as a powerful tyrosinase inhibitor like kojic acid or arbutin, although toxicity must be considered under experimental conditions.In addition, further study will be needed to determine whether signaling pathways such as cAMP-PKA-CREB, which are upstream signaling pathways that regulate MITF-tyrosinase signaling, are inhibited.
In this study, the morphology and epidermal pigmentation were normal during the whole period of study (Figure 5A,B, macroscopic view).However, epidermal hyperdifferentiation was also observed through histological observation (Figure 5D).This is a unique feature of MelanoDerm that we have observed in previous studies [10,[23][24][25].However, it is also necessary to comprehensively examine whether this phenomenon affected the epidermal pigmentation.Macroscopic observations clearly demonstrated the difference in pigmentation of the epidermis according to the substance treatment.Epidermal pigmentation was significantly suppressed via kojic acid as a positive control, and the concentration-dependent suppression of epidermal pigmentation was also observed via the test substance.Furthermore, the Fontana-Masson's (F-M) staining results clearly demonstrate the difference in the amount of melanin accumulated in the epidermis.Therefore, although there was some degree of epidermal hyper-differentiation, these results show that epidermal pigmentation was normal in this model.However, because it is not sufficient to demonstrate the viability of melanocytes through F-M staining alone, we are planning to reinforce this through follow-up studies.In addition, many other cells in the skin, such as immune cells and dermal fibroblasts, could affect skin pigmentation [26][27][28][29].However, MelanoDerm consists only of keratinocytes and melanocytes.So, it also has limitations in representing the complex pigmentation reactions that occur in native skin.

General Experimental Procedure
Low-resolution LC/MS measurements were performed using the Agilent Technologies 1260 quadrupole (Agilent Technologies, Santa Clara, CA, USA) and Waters Micromass ZQ LC/MS system (Waters Corp, Milford, MA, USA) using a reversed-phase column (Phenomenex, Torrance, CA, USA) (Phenomenex Luna C18 (2) 100 Å, 50 mm × 4.6 mm, 5 µm) at a flow rate of 1.0 mL/min at the National Research Facilities and Equipment Center (NanoBioEnergy Materials Center) at Ewha Womans University.The NMR spectra were obtained using an Agilent NMR spectrometer (Agilent, Santa Clara, CA, USA) at 400 MHz for 1 H and at 100 MHz for 13 C using the signals of the residual solvent as internal references (δ H 7.24 ppm and δ C 77.2 ppm for deuterated chloroform [CDCl 3 ]).High-resolution EI-MS spectra were acquired using a JEOL JMS-AX505WA mass spectrometer (JEOL Ltd., Tokyo, Japan) at Seoul National University.

Collection and Phylogenetic Analysis of Strain APmarine135
The marine-derived Bacillus sp.strain APmarine135 was isolated from a stony coral, Scleractinia, collected from the Federated States of Micronesia.The strain was identified as a Bacillus sp.based on 16S rRNA gene sequence analysis (accession number NR_025264.1).

Cultivation, Extraction, and Isolation
The Bacillus sp.APmarine135 was cultivated in 54 L of a SYP medium (10 g/L of soluble starch, 4 g/L of yeast, 2 g/L of peptone, and 34.25 g/L of sea salt in 1 L of distilled water) for 3 days at 27 • C under constant shaking at 80 rpm.After 60 h, a sterilized HP-20 resin (5.4 L) was added, followed by further incubation for 12 h, after which the resin was collected and washed four times (30 min each) with 54 L of 20% acetone (H 2 O/acetone, 80/20 by volume).Finally, the resin was eluted with 54 L of 99.5% acetone for 24 h under constant shaking.Acetone was removed under reduced pressure, and the resulting crude extract (3.5 g) was fractionated via medium-pressure liquid chromatography (MPLC) using a silica column.The mobile phases A and B were n-hexane and chloroform, respectively.The samples were run for 60 min at a flow rate of 20 mL/min with the following gradient program for solvent B: 0 to 10.9 min, 0%; 10 to 21.8 min, 0 to 11.9%; 21.8 to 26 min, 11.9%; 26 to 37 min, 11.9 to 26%; 37 to 43 min, 26%; 43 to 52.6 min, 26 to 100%; and 52.6 to 60 min and 100% to obtain fractions M1-M7.The sample was eluted with 100% methanol for 25 min and labeled M8.Fraction M3 was purified using preparative HPLC (Phenomenex Luna C18 [2] 100 Å, 250 mm × 21.2 mm).The mobile phases A and B were water and acetonitrile, respectively.The sample was run for 30 min at a flow rate of 15 mL/min using the following gradient program for solvent B: 0 to 5 min, 75%; and 5 to 25 min, 75 to 95%; 25 to 30 min, 95% to yield 2,4,6-triphenyl-1-hexene (1, t R 20.0 min, 36 mg).

Cell Viability Assay
Cell viability was determined using the Quanti-MAX™ WST-8 Cell Viability Assay Kit (Biomax, Seoul, Republic of Korea) according to the manufacturer's protocols.Cells were seeded in a 96-well plate (8000 cells/well) for 24 h, and the culture medium was replaced with a fresh culture medium containing 2,4,6-triphenyl-1-hexene diluted to the indicated concentrations.After 72 h, cell viability was assessed by replacing the medium with an appropriate medium containing a 10% WST-8 solution.The plate was incubated for 1 h, and absorbance was measured at 450 nm using a Microplate Reader (BioTek, Winooski, VT, USA).Cell viability was calculated using the following formula: cell viability (%) = (optical density (450 nm) of the experimental group/optical density of the control group) × 100.

Measurement of Melanin Content
To quantify melanin content, B16 cells (2 × 10 4 cells/well in 48-well plates) were cultured for 24 h, followed by pretreatment with increasing concentrations of 2,4,6-triphenyl-1-hexene (1) for 6 h.Thereafter, α-MSH (0.1 µM) was added to induce melanin production in a phenol red-free cell culture medium.After 72 h, 1N NaOH was added to each well to measure the intracellular melanin content, and the plate was heated to 60 • C for 30 min.The resulting lysate was aliquoted into a 96-well plate, and the absorbance was determined at 405 nm.Intracellular melanin content was normalized to the total protein content.Melanin levels were calculated via comparison with those of the corresponding controls and are shown as percentages.

Cellular Tyrosinase Activity Assay
Cellular tyrosinase activity was estimated by measuring oxidase activity.Briefly, B16 cells were lysed in 1 mL of a sodium phosphate buffer (0.1 M, pH 6.8) containing 1% Triton X-100 for 20 min, followed by centrifugation at 13,000 rpm for 20 min at 4 • C. The supernatant and substrate solution (10 mM L-DOPA or 0.03% L-tyrosine) were dispensed in equal volumes into a 96-well plate, followed by the addition of 2,4,6-triphenyl-1-hexene (1).The cellular tyrosinase activity was determined at 475 nm using a spectrophotometer at least 5 times over 10 at an incubation temperature of 37 • C.

Western Blot Analysis
Briefly, B16 cells were cultured in 6-well plates, followed by treatment with 2,4,6triphenyl-1-hexene (1).The next day, the cells were washed twice with cold PBS, and total intracellular proteins were extracted on ice for 20 min using the RIPA buffer 1X (Cell Signaling Technology, Danvers, MA, USA) supplemented with a 1:200 dilution of a protease inhibitor cocktail III and phosphatase inhibitor cocktail set III (Calbiochem Biosciences, La Jolla, CA, USA).After centrifugation at 13,000 rpm and 4 • C, the supernatant was collected, and the total protein content was determined using a Pierce bicinchoninic acid (BCA) protein assay kit.Equal amounts of soluble proteins were resolved using 10% SDS-PAGE and transferred to a nitrocellulose membrane (BioRad, Hercules, CA, USA) in a cold transfer buffer (25 mM Tris, 192 mM glycine, and 20% (w/v) MeOH) for 90 min at 280 mA.Thereafter, the membranes were blocked for at least 1 h with TBS 1X supplemented with a 5% blotting-grade blocker (BioRad) and incubated overnight at 4 • C with primary antibodies diluted to the appropriate concentration (as per the provided data sheet) in 1X TBS.Primary antibodies against β-actin (#ab3280) and tyrosinase (#ab52493) were purchased from Abcam (Cambridge, UK).Following overnight incubation, the membranes were further incubated with secondary antibodies and enhanced using a Clarity™ Western ECL substrate (ECL solution; BioRad).Goat anti-rabbit IgG (HRP) (#ab6721) and rabbit anti-mouse IgG (HRP) (#ab6728) secondary antibodies were purchased from Abcam (Cambridge, UK).Images of the blotted membranes were captured using an iBright™ CL750 Imaging System (Invitrogen, Carlsbad, CA, USA).The expression levels of the proteins were normalized to those of endogenous actin.

Real-Time PCR
To determine the mRNA expression levels of melanogenesis-related genes, B16 cells were cultured in 6-well plates and treated with 2,4,6-triphenyl-1-hexene (1).The next day, the cells were washed twice with cold PBS, and the total RNA was extracted from cell lysates using a TRIzol reagent (Thermo Fisher Scientific, Waltham, MA, USA) according to the manufacturer's instructions.Complimentary DNA was synthesized from total mRNA using the GoScript™ Reverse Transcription System (Promega, Madison, WI, USA) and a thermal cycler (T-100; BioRad).The PCR amplification of the target cDNA was performed on the CFX Connect Optics Module (BioRad) using iQ SYBR ® Green Supermix (BioRad) and specific primers.The mRNA levels of the target genes were normalized to those of β-actin.Specific primers were purchased from BioRad Laboratories.

Evaluation of Skin-Whitening Efficacy Using a 3D Reconstructed Skin Model
The MelanoDerm (MEL-300-B, MatTek Corp., Ashland, MA, USA) was incubated in an EPI-100-NMM-113-PRF medium (MatTek Corp., Ashland, MA, USA) at 37 • C in a humidified 5% CO 2 incubator.The MelanoDerm used in this experiment was MEL-300-B, and it was manufactured using keratinocytes and melanocytes derived from the neonatal foreskin of African-American babies.MelanoDerm was treated with different concentrations of 2,4,6-triphenyl-1-hexene (1) every other day for 14 days.Epidermal pigmentation was examined via optical and histological observations.Epidermal pigmentation was calculated by comparing variations in L values (a lightness/darkness index) on days 1 and 14 and estimating the difference between them (∆L).For histological examination, tissues were fixed in 10% neutral buffered formalin (BBC Biochemical, Mount Vernon, WA, USA), embedded in paraffin, and cut into 5 µm sections.Thereafter, the sections were stained with hematoxylin and eosin (H&E) and Fontana-Masson's (F-M) and imaged.

Conclusions
In this study, we identified 2,4,6-triphenyl-1-hexene (1) as a potent skin-whitening agent derived from the marine microorganism of APmarine 135.We demonstrated that 2,4,6-triphenyl-1-hexene (1) suppressed melanin synthesis and simultaneously reduced both the activity and expression of tyrosinase in B16 cells.Then, we verified its skinwhitening effect using a 3D human-pigmented epidermis model, MelanoDerm.Based on these results, we conclude that marine microorganisms are a good source of biologically active compounds and further suggest that 2,4,6-triphenyl-1-hexene (1) is a promising anti-melanogenic agent in the cosmetic and pharmaceutical field.

Figure 2 .
Figure 2. Concentration-dependent anti-melanogenic effect of APmarine135 in B16 cells.Effects of incubation with the indicated concentrations of APmarine135 for 72 h on intracellular melanin contents in α-MSH-stimulated B16 cells.APmarine135 sample conditions are 10%, 20%, 30% (A), 50% and 100% (B), rexpectively.Intracellular melanin content was determined by measuring the absorbance of B16 cell lysates at 405 nm and normalizing to the protein content, which was determined using a protein assay kit.Results are presented as mean ± standard deviation (SD), expressed as a percentage relative to the control group.(### p < 0.001 vs. control group, ** p < 0.01, *** p < 0.001 vs. α-MSH-treated group).

Figure 2 .
Figure 2. Concentration-dependent anti-melanogenic effect of APmarine135 in B16 cells.Effects of incubation with the indicated concentrations of APmarine135 for 72 h on intracellular melanin contents in α-MSH-stimulated B16 cells.APmarine135 sample conditions are 10%, 20%, 30% (A), 50% and 100% (B), rexpectively.Intracellular melanin content was determined by measuring the absorbance of B16 cell lysates at 405 nm and normalizing to the protein content, which was determined using a protein assay kit.Results are presented as mean ± standard deviation (SD), expressed as a percentage relative to the control group.(### p < 0.001 vs. control group, ** p < 0.01, *** p < 0.001 vs. α-MSH-treated group).

Figure 3 .
Figure 3. Anti-melanogenic effects of non-toxic concentrations of 2,4,6-triphenyl-1-hexene in B16 melanoma cells.(A) Effect of 2,4,6-triphenyl-1-hexene on B16 cell viability.B16 cells were treated with the indicated concentrations of 2,4,6-triphenyl-1-hexene for 72 h, and cell viability was estimated using a CCK-8 assay kit.(B) Effects of incubation with the indicated concentrations of 2,4,6triphenyl-1-hexene for 72 h on intracellular melanin content in α-MSH-stimulated B16 cells.Intracellular melanin content was determined by measuring the absorbance of B16 cell lysates at 405 nm and normalizing the obtained values to the protein content, which was determined using a protein assay kit.Results are presented as mean ± standard deviation (SD), expressed as a percentage relative to the control group.(C) Microscopic images of B16 cells under the same conditions as above.Figures depict results from at least three replicate experiments.Results are presented as mean ± SD, expressed as a percentage relative to the control or α-MSH-treated group."-" means non-treated or without any treatment, and "+" means treated with the indicated compound along with α-MSH at a concentration of 0.1 µM where indicated.Scale bar in (C) = 50 µm.(A; * p < 0.05, ** p < 0.01, *** p < 0.001 vs. control group, B; ### p < 0.001 vs. control group, * p < 0.05, *** p < 0.001 vs. α-MSH-treated group).

Figure 3 .
Figure 3. Anti-melanogenic effects of non-toxic concentrations of 2,4,6-triphenyl-1-hexene in B16 melanoma cells.(A) Effect of 2,4,6-triphenyl-1-hexene on B16 cell viability.B16 cells were treated with the indicated concentrations of 2,4,6-triphenyl-1-hexene for 72 h, and cell viability was estimated using a CCK-8 assay kit.(B) Effects of incubation with the indicated concentrations of 2,4,6-triphenyl-1-hexene for 72 h on intracellular melanin content in α-MSH-stimulated B16 cells.Intracellular melanin content was determined by measuring the absorbance of B16 cell lysates at 405 nm and normalizing the obtained values to the protein content, which was determined using a protein assay kit.Results are presented as mean ± standard deviation (SD), expressed as a percentage relative to the control group.(C) Microscopic images of B16 cells under the same conditions as above.Figures depict results from at least three replicate experiments.Results are presented as mean ± SD, expressed as a percentage relative to the control or α-MSH-treated group."-" means non-treated or without any treatment, and "+" means treated with the indicated compound along with α-MSH at a concentration of 0.1 µM where indicated.Scale bar in (C) = 50 µm.(A; * p < 0.05, ** p < 0.01, *** p < 0.001 vs. control group, B; ### p < 0.001 vs. control group, * p < 0.05, *** p < 0.001 vs. α-MSH-treated group).