A Frog Peptide Ameliorates Skin Photoaging Through Scavenging Reactive Oxygen Species
Open accessAbstract
Although many bioactive peptides have been identified from the frog skins, their protective effects and the molecular mechanisms against skin photodamage are still poorly understood. In this study, a novel 20-residue peptide (antioxidin-NV, GWANTLKNVAGGLCKMTGAA) was characterized from the skin of plateau frog Nanorana ventripunctata . Antioxidin-NV obviously decreased skin erythema, thickness and wrinkle formation induced by Ultraviolet (UV) B exposure in hairless mice. In UVB-irradiated keratinocytes (HaCaT cells) and hairless mice, it effectively inhibited DNA damage through reducing p-Histone H2A.X (γH2AX) expression, alleviated cell apoptosis by decreasing the expression of apoptosis-specific protein (cleaved caspase 3), and reduced interleukin-6 (IL-6) production via blocking UVB-activated Toll-like receptor 4 (TLR4)/p38/JNK/NF-κB signaling. In UVB-irradiated human skin fibroblasts (HSF cells) and hairless mice, it effectively restored HSF cells survival rate, and rescued α-SMA accumulation and collagen (especially type I collagen) production by restoring transforming growth factor-β1 (TGF-β1)/Smad2 signaling. We found that antioxidin-NV directly and rapidly scavenged intracellular and mitochondrial ROS in HaCaT cells upon UVB irradiation, and quickly eliminated the artificial free radicals, 2, 2′-azinobis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS + ). Taken together, antioxidin-NV directly and rapidly scavenged excessive ROS upon UVB irradiation, subsequently alleviated UVB-induced DNA damage, cell apoptosis, and inflammatory response, thus protecting against UVB-induced skin photoaging. These properties makes antioxidin-NV an excellent candidate for the development of novel anti-photoaging agent.
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Written from the paper’s full text.
TL;DR
Antioxidin-NV, a novel 20-residue frog-skin peptide from *Nanorana ventripunctata*, directly scavenges ROS and protects against UVB-induced skin photoaging in cells and hairless mice. It reduces DNA damage, apoptosis, inflammation, and restores collagen production via TGF-β1/Smad2 signaling.
Key findings
- Antioxidin-NV (GWANTLKNVAGGLCKMTGAA) was isolated and characterized; MALDI-TOF MS measured 1963.70 Da versus calculated 1963.30 Da, and its precursor is 72 amino acids with a 24-residue signal peptide, 28-residue acidic region, and 20-residue mature peptide.
- It rapidly scavenged ABTS+ in a dose- and time-dependent manner: at 80 μg/ml, 96% within 1 min and nearly 99% within 8 min; at 5 μg/ml, 40% within 4 min.
- In UVB-irradiated HaCaT cells, apoptosis was 43.26% with UVB alone and 14.44% with antioxidin-NV at 40 μg/ml; it also reduced γH2AX, cleaved caspase 3, and IL-6 via blocking TLR4/p38/JNK/NF-κB signaling.
- In UVB-irradiated hairless mice, topical antioxidin-NV reduced erythema, epidermal thickness, and wrinkle formation, restored α-SMA and type I collagen, and increased TGF-β1/Smad2 signaling; scrambled sNV had no significant therapeutic effect.
Methods
- Peptide purification and characterization: skin secretions from *N. ventripunctata* (n = 30; 20–25 g) were fractionated by Sephadex G-50 and C18 RP-HPLC, then analyzed by Edman degradation, MALDI-TOF MS, and cDNA cloning; antioxidin-NV and scrambled sNV were synthesized.
- In vitro assays: HaCaT keratinocytes and HSF cells were UVB-irradiated at 80 mJ/cm² and treated with antioxidin-NV (10, 20, 40 μg/ml) or vitamin C (40 μg/ml); outcomes included ABTS+ scavenging, intracellular/mitochondrial ROS, MTT cytotoxicity, hemolysis, DNA fragmentation, western blot, immunofluorescence, flow cytometry, and ELISA.
- In vivo model: male SKH-1 hairless mice (n = 30, 6–8 weeks old, 20–30 g) were randomized into five groups of six; UVB was 100 mJ/cm² five times in week 1 then 200 mJ/cm² three times/week for 12 weeks, with topical 100 μl of 200 μg/ml antioxidin-NV, vitamin C, PBS, or sNV; skin was analyzed by H&E, Masson stain, IHC, immunofluorescence, western blot, and ELISA, with statistics by Student’s t-test or one-way ANOVA (p < 0.05).
Limitations
- The paper states that the effects of antioxidin-NV on DNA damage-related signaling pathways need further investigation to clarify its protective mechanism in vitro and in vivo.
- The paper reports no adverse effects on body weight, general health, or behavior with topical antioxidin-NV, but does not present a dedicated long-term toxicity or safety study.
- Evident from the text: the in vivo work uses only male SKH-1 hairless mice, a single topical mouse dose (200 μg/ml), and no human data; in vitro experiments report n = 3 and in vivo n = 6, limiting broader generalization.
Model-written summary. Check it against the paper before relying on it.
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Claims the paper makes
0 of 31 cited sources checked · 0 supported · 0 flagged
- Findingown data
Antioxidin-NV decreased skin erythema, thickness and wrinkle formation induced by UVB exposure in hairless mice.
“Antioxidin-NV obviously decreased skin erythema, thickness and wrinkle formation induced by Ultraviolet (UV) B exposure in hairless mice.”
- Also stated in: § Antioxidin-NV Suppressed UVB-Induced Skin Photoaging in Hairless Mice · boosted
“topical application of antioxidin-NV significantly suppressed UVB-induced skin photoaging in hairless mice with reduced skin erythema, hyperplasia, wrinkling, and roughness compared to PBS-treated mice.”
Quote in the paperSubstantial claim - Also stated in: § Antioxidin-NV Suppressed UVB-Induced Skin Photoaging in Hairless Mice · boosted
- Findingown data
In UVB-irradiated HSF cells and hairless mice, antioxidin-NV rescued α-SMA accumulation and collagen (especially type I collagen) production by restoring TGF-β1/Smad2 signaling.
“rescued α-SMA accumulation and collagen (especially type I collagen) production by restoring transforming growth factor-β1 (TGF-β1)/Smad2 signaling.”
Quote in the paperSubstantial claim - Findingown data
In UVB-irradiated HaCaT cells and hairless mice, antioxidin-NV inhibited DNA damage through reducing γH2AX expression.
“In UVB-irradiated keratinocytes (HaCaT cells) and hairless mice, it effectively inhibited DNA damage through reducing p-Histone H2A.X (γH2AX) expression”
- Also stated in: § Antioxidin-NV Inhibited UVB-Induced DNA Damage in HaCaT Cells and Hairless Mice by Reducing p-Histone H2A.X (γH2AX) Expression · plain
“However, antioxidin-NV significantly reduced γH2AX expression in HaCaT cells induced by UVB irradiation in a dose-dependent manner (Figures 4B,C).”
Quote in the paperSubstantial claim - Also stated in: § Antioxidin-NV Inhibited UVB-Induced DNA Damage in HaCaT Cells and Hairless Mice by Reducing p-Histone H2A.X (γH2AX) Expression · plain
- Findingown data
A novel 20-residue peptide (antioxidin-NV, GWANTLKNVAGGLCKMTGAA) was characterized from the skin of the plateau frog Nanorana ventripunctata.
“In this study, a novel 20-residue peptide (antioxidin-NV, GWANTLKNVAGGLCKMTGAA) was characterized from the skin of plateau frog Nanorana ventripunctata.”
- Also stated in: § Isolation and Characterization of Antioxidin-NV · plain
“The purified peptide was designated as antioxidin-NV (Supplementary Figure S1C).”
Quote in the paperSubstantial claim - Also stated in: § Isolation and Characterization of Antioxidin-NV · plain
- Findingown data
In UVB-irradiated HaCaT cells and hairless mice, antioxidin-NV alleviated cell apoptosis by decreasing cleaved caspase 3 expression.
“alleviated cell apoptosis by decreasing the expression of apoptosis-specific protein (cleaved caspase 3)”
- Also stated in: § Antioxidin-NV Inhibited UVB-Induced Cell Apoptosis in HaCaT Cells and Hairless Mice · plain
“Immunofluorescence and western blot analysis showed that antioxidin-NV significantly reduced the expression of apoptotic protein cleaved caspase 3 (a marker protein for apoptosis) in the UVB-irradiated HaCaT cells in a dose-dependent manner (Figures 5B,C).”
Quote in the paperSubstantial claim - Also stated in: § Antioxidin-NV Inhibited UVB-Induced Cell Apoptosis in HaCaT Cells and Hairless Mice · plain
- Findingown data
In UVB-irradiated HaCaT cells and hairless mice, antioxidin-NV reduced IL-6 production via blocking UVB-activated TLR4/p38/JNK/NF-κB signaling.
“reduced interleukin-6 (IL-6) production via blocking UVB-activated Toll-like receptor 4 (TLR4)/p38/JNK/NF-κB signaling.”
Quote in the paperSubstantial claim - Findingown data
Antioxidin-NV directly and rapidly scavenged intracellular and mitochondrial ROS in HaCaT cells upon UVB irradiation.
“We found that antioxidin-NV directly and rapidly scavenged intracellular and mitochondrial ROS in HaCaT cells upon UVB irradiation”
- Also stated in: § Antioxidin-NV Rapidly Eliminated Artificial ABTS+ Radicals and Scavenged Intracellular/Mitochondrial ROS · plain
“the addition of antioxidin-NV significantly decreased the intracellular ROS level in HaCaT cells upon UVB irradiation (Figures 2B,C).”
- Also stated in: § Antioxidin-NV Rapidly Eliminated Artificial ABTS+ Radicals and Scavenged Intracellular/Mitochondrial ROS · plain
“Furthermore, antioxidin-NV effectively cleared the ROS in mitochondria induced by UVB irradiation (Figure 2D).”
Quote in the paperSubstantial claim - Also stated in: § Antioxidin-NV Rapidly Eliminated Artificial ABTS+ Radicals and Scavenged Intracellular/Mitochondrial ROS · plain
- Findingown data
In UVB-irradiated HSF cells and hairless mice, antioxidin-NV restored HSF cell survival rate.
“In UVB-irradiated human skin fibroblasts (HSF cells) and hairless mice, it effectively restored HSF cells survival rate”
Quote in the paperSubstantial claim - Findingown data
Antioxidin-NV quickly eliminated artificial free radicals ABTS+.
“and quickly eliminated the artificial free radicals, 2, 2′-azinobis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS+).”
- Also stated in: § Antioxidin-NV Rapidly Eliminated Artificial ABTS+ Radicals and Scavenged Intracellular/Mitochondrial ROS · hedged
“As illustrated in Figure 2A, antioxidin-NV could rapidly scavenge ABTS+ in a dose-dependent manner.”
Quote in the paperSubstantial claim - Also stated in: § Antioxidin-NV Rapidly Eliminated Artificial ABTS+ Radicals and Scavenged Intracellular/Mitochondrial ROS · hedged
- Findingown data
Antioxidin-NV treatment significantly increased TGF-β1 production in UVB-irradiated HSF compared with PBS treatment in a dose-dependent manner.
“antioxidin-NV treatment significantly increased TGF-β1 production in UVB-irradiated HSF compared with PBS treatment in a dose-dependent manner”
- Also stated in: § Discussion · plain
“Antioxidin-NV significantly increased UVB-inhibited TGF-β1 secretion in a dose-dependent manner in HaCaT cells.”
Quote in the paperSubstantial claim - Also stated in: § Discussion · plain
- Findingown data
A progressive increment of intracellular ROS level was observed in UVB-irradiated HaCaT cells.
“A progressive increment of intracellular ROS level was observed in the UVB-irradiated HaCaT cells”
Quote in the paperSubstantial claim - Findingown data
Even at the concentration down to 5 μg/ml, 40% ABTS+ was scavenged within 4 min by antioxidin-NV.
“Even the concentration down to 5 μg/ml, 40% ABTS+ was scavenged within 4 min by antioxidin-NV.”
Quote in the paperSubstantial claim - Findingown data
UVB exposure suppressed TGF-β1 production in the skin of hairless mice.
“UVB exposure also suppressed TGF-β1 production in the skin of hairless mice”
Quote in the paperSubstantial claim - Findingown data
The scavenging efficacy of UVB-induced intracellular ROS by antioxidin-NV is comparable to the ROS inhibitor N-acetyl-L-cysteine (NAC).
“The scavenging efficacy of UVB-induced intracellular ROS is comparable to the ROS inhibitor, N-acetyl-L-cysteine (NAC) (Figures 2B,C).”
Quote in the paperSubstantial claim - Findingown data
UVB irradiation directly inhibited HSF survival rate.
“UVB irradiation directly inhibited HSF survival rate”
Quote in the paperSubstantial claim - Findingown data
UVB irradiation produced a typical ladder with clearly increased intensity of DNA fragmentation in HaCaT cells.
“Agarose gel electrophoresis showed that UVB irradiation produced a typical ladder with clearly increased intensity of DNA fragmentation in HaCaT cells”
Quote in the paperSubstantial claim - Findingown data
Antioxidin-NV significantly reduced DNA fragmentation formation in HaCaT cells in a dose-dependent manner.
“antioxidin-NV significantly reduced its formation in a dose-dependent manner (Figure 4A).”
Quote in the paperSubstantial claim - Findingown data
Topical application of antioxidin-NV significantly decreased the secretion of IL-6 compared to PBS treatment in UVB-irradiated hairless mice.
“the topical application of antioxidin-NV significantly decreased the secretion of IL-6 compared to PBS treatment”
Quote in the paperSubstantial claim - Findingown data
Antioxidin-NV effectively suppressed the secretion of IL-6 in a dose-dependent manner in UVB-exposed HaCaT cells.
“antioxidin-NV effiectively suppressed the secretion of IL-6 in a dose-dependent manner”
Quote in the paperSubstantial claim - Findingown data
The amino acid sequence of antioxidin-NV was identified as GWANTLKNVAGGLCKMTGAA.
“After Edman degradation, the amino acid sequence of antioxidin-NV was identified as GWANTLKNVAGGLCKMTGAA.”
Quote in the paperNot a substantial claim - Findingown data
After treatment by TLR4 inhibitor MTS510, the inhibitory effect of antioxidin-NV on NF-κB p65 phosphorylation in UVB-irradiated HaCaT cells was completely inhibited.
“after the treatment by TLR4 inhibitor MTS510, the inhibitory effect of antioxidin-NV on NF-κB p65 phosphorylation in UVB-irradiated HaCaT cells was completely inhibited”
Quote in the paperSubstantial claim - Findingown data
UVB irradiation markedly increased the expression of cleaved caspase-3 in the skin of hairless mice.
“Immunofluorescence, IHC and western blot analysis showed that UVB irradiation markedly increased the expression of cleaved caspase-3 in the skin of hairless mice”
Quote in the paperSubstantial claim - Findingown data
The scrambled antioxidin-NV (sNV, isotype control) had no significant therapeutic effects on UVB-induced skin photoaging.
“The scrambled antioxidin-NV (sNV, isotype control) had no significant therapeutic effects on UVB-induced skin photoaging”
Quote in the paperSubstantial claim - Findingown data
UVB irradiation markedly resulted in a reduction of collagen I deposition in the skin of hairless mice.
“UVB irradiation markedly resulted in a reduction of collagen I deposition in the skin of hairless mice”
Quote in the paperSubstantial claim - Findingown data
Topical application of antioxidin-NV reduced UVB-induced γH2AX expression in hairless mice.
“but topical application of antioxidin-NV reduced UVB-induced γH2AX expression (Figure 4D).”
Quote in the paperSubstantial claim - Findingown data
Antioxidin-NV obviously restored HSF cells survival rate post UVB irradiation in a concentration-dependent manner.
“antioxidin-NV obviously restored HSF cells survival rate post UVB irradiation in a concentration-dependent manner”
- Also stated in: § Discussion · plain
“Antioxidin-NV restored the survival rate of HSF cells upon UVB irradiation in a concentration-dependent manner in vitro.”
Quote in the paperSubstantial claim - Also stated in: § Discussion · plain
- Findingown data
UVB exposure resulted in apoptosis of HaCaT cells (43.26%).
“As illustrated in Figure 5A, UVB exposure resulted in the apoptosis of HaCaT cells (43.26%)”
Quote in the paperSubstantial claim - Findingown data
UVB irradiation increased IL-6 production in the skins of hairless mice.
“UVB irradiation increased IL-6 production in the skins of hairless mice”
Quote in the paperSubstantial claim - Findingown data
UVB irradiation markedly increased JNK, p38, IkBα and p65 phosphorylation in HaCaT cells.
“UVB irradiation markedly increased JNK, p38, IkBα and p65 phosphorylation in HaCaT cells”
Quote in the paperSubstantial claim - Findingown data
UVB irradiation obviously increased the secretion of IL-6 in UVB-exposed HaCaT cells.
“UVB irradiation obviously increased the secretion of IL-6 in UVB-exposed HaCaT cells”
Quote in the paperSubstantial claim - Findingown data
Antioxidin-NV significantly decreased UVB-induced JNK, p38, IkBα and p65 phosphorylation in a concentration-dependent manner in HaCaT cells.
“antioxidin-NV significantly decreased UVB-induced JNK, p38, IkBα and p65 phosphorylation in a concentration-dependent manner”
- Also stated in: § Discussion · plain
“Antioxidin-NV significantly decreased JNK, p38, IkBα and NF-κB p65 phosphorylation.”
Quote in the paperSubstantial claim - Also stated in: § Discussion · plain
- Findingown data
UVB irradiation obviously induced skin photoaging in hairless mice.
“As illustrated in Figure 3A, UVB irradiation obviously induced skin photoaging in hairless mice”
Quote in the paperSubstantial claim - Findingown data
UVB irradiation resulted in a significant increment of γH2AX expression in HaCaT cells.
“Western blot analysis and immunofluorescence staining further showed that UVB irradiation resulted in a significant increment of p-Histone H2A.X (γH2AX) expression, a marker protein for DNA damage.”
Quote in the paperSubstantial claim - Findingown data
Antioxidin-NV treatment markedly increased the abundance and density of collagen fibers in UVB-irradiated skins compared to PBS treatment.
“antioxidin-NV treatment markedly increased the abundance and density of collagen fibers in UVB-irradiated skins compared to PBS treatment”
Quote in the paperSubstantial claim - Findingown data
Antioxidin-NV showed a better therapeutic efficacy against UVB-induced skin photoaging than vitamin C.
“To our surprise, antioxidin-NV showed a better therapeutic efficacy against UVB-induced skin photoaging than vitamin C (VC, positive control) (Figures 3A–C).”
Quote in the paperSubstantial claim - Findingown data
UVB irradiation obviously reduced the expression of α-SMA in the skin of UVB-exposed mice.
“UVB irradiation obviously reduced the expression of α-SMA in the skin of UVB-exposed mice”
Quote in the paperSubstantial claim - Findingown data
The purine receptor inhibitor KN-62 and G protein coupling receptor inhibitor PTX had no significant effect on antioxidin-NV-mediated IL-6 down-regulation in UVB-irradiated HaCaT cells.
“The purine receptor inhibitor KN-62 (2 μM) and G protein coupling receptor inhibitor PTX (10 μg/ml) had no significant effect on antioxidin-NV-mediated IL-6 down-regulation”
Quote in the paperSubstantial claim - Findingown data
Antioxidin-NV (40 μg/ml) treatment reduced UVB-induced HaCaT cell apoptosis at both the early and late stages (14.44%).
“while antioxidin-NV (40 μg/ml) treatment reduced UVB-induced HaCaT cell apoptosis at both the early and late stages (14.44%).”
Quote in the paperSubstantial claim - Findingown data
Topical application of antioxidin-NV greatly suppressed UVB-induced skin erythema, thickness and wrinkle formation in hairless mice.
“Our results revealed that topical application of antioxidin-NV greatly suppressed UVB-induced skin erythema, thickness and wrinkle formation in hairless mice”
Quote in the paperSubstantial claim - Findingown data
In UVB-irradiated hairless mice, antioxidin-NV significantly decreased JNK, p38, IkBα and p65 phosphorylation.
“The same results were observed in UVB-irradiated hairless mice, antioxidin-NV also significantly decreased JNK, p38, IkBα and p65 phosphorylation”
Quote in the paperSubstantial claim - Findingown data
Antioxidin-NV treatment significantly rescued collagen I production in hairless mice post UVB irradiation.
“antioxidin-NV treatment significantly rescued collagen I production in hairless mice post UVB irradiation”
- Also stated in: § Discussion · plain
“Antioxidin-NV significantly rescued the collagen and type I collagen production in HSF cells of the skin tissues after UVB irradiation”
Quote in the paperSubstantial claim - Also stated in: § Discussion · plain
- Findingown data
Antioxidin-NV significantly suppressed UVB-induced skin photoaging in hairless mice.
“Given the above observation that antioxidin-NV significantly suppressed UVB-induced skin photoaging in hairless mice”
Quote in the paperSubstantial claim - Findingown data
Topical application of antioxidin-NV significantly increased TGF-β1 production in the skin of UVB-irradiated hairless mice compared with PBS treatment.
“topical application of antioxidin-NV significantly increased TGF-β1 production in the skin of UVB-irradiated hairless mice compared with PBS treatment”
- Also stated in: § Discussion · plain
“Antioxidin-NV also significantly upregulated TGF-β1 levels in UVB-induced skin tissues in vivo.”
Quote in the paperSubstantial claim - Also stated in: § Discussion · plain
- Findingown data
The deduced amino acid sequence of antioxidin-NV is completely consistent with that sequenced by Edman degradation.
“As shown in Figure 1, the deduced amino acid sequence of antioxidin-NV is completely consistent with that sequenced by Edman degradation.”
Quote in the paperNot a substantial claim - Findingown data
UVB irradiation obviously suppressed TGF-β1 production in HSF cells.
“UVB irradiation obviously suppressed TGF-β1 production in HSF cells”
Quote in the paperSubstantial claim - Findingown data
After the addition of TLR4 inhibitor MTS510, antioxidin-NV-mediated IL-6 down-regulation in UVB-irradiated HaCaT cells was completely inhibited.
“After the addition of TLR4 inhibitor MTS510 (10 μg/ml), antioxidin-NV-mediated IL-6 down-regulation in UVB-irradiated HaCaT cells was completely inhibited”
- Also stated in: § Discussion · plain
“after the treatment by TLR4 inhibitor MTS510, IL-6 down-regulation induced by antioxidin-NV was completely inhibited”
Quote in the paperSubstantial claim - Also stated in: § Discussion · plain
- Findingown data
The cDNA clone encoding the precursor of antioxidin-NV was sequenced from the skin cDNA library of N. ventripunctata (GenBank accession number: MW114946).
“The cDNA clone encoding the precursor of antioxidin-NV was sequenced from the skin cDNA library of N. ventripunctata (GenBank accession number: MW114946).”
Quote in the paperNot a substantial claim - Findingown data
A higher accumulation of α-SMA positive staining was observed in NV treatment compared to PBS in UVB-exposed mice.
“a higher accumulation of a-SMA positive staining was observed in NV treatment when compared to PBS”
- Also stated in: § Discussion · plain
“antioxidin-NV significantly restored UVB-reduced α-SMA expression in vivo.”
Quote in the paperSubstantial claim - Also stated in: § Discussion · plain
- Findingown data
Antioxidin-NV significantly suppressed intracellular and mitochondria ROS generation.
“antioxidin-NV significantly suppressed intracellular and mitochondria ROS generation”
Quote in the paperSubstantial claim - Findingown data
UVB irradiation markedly reduced Smad2 phosphorylation in HSF cells.
“UVB irradiation markedly reduced Smad2 phosphorylation in HSF cells”
Quote in the paperSubstantial claim - Findingown data
Collagen fibers of mice without UVB irradiation (sham) were dense and regular.
“the collagen fibers of mice without UVB irradiation (sham) were dense and regular”
Quote in the paperNot a substantial claim - Findingown data
Antioxidin-NV significantly inhibited the expression of cleaved caspase-3 in the skin of hairless mice induced by UVB irradiation.
“But antioxidin-NV significantly inhibited the expression of cleaved caspase-3 in the skin of hairless mice induced by UVB irradiation”
Quote in the paperSubstantial claim - Findingown data
Antioxidin-NV obviously increased Smad2 phosphorylation in UVB-irradiated HSF cells compared to PBS-treated cells in a dose-dependent manner.
“antioxidin-NV obviously increased Smad2 phosphorylation in UVB-irradiated HSF cells compared to PBS-treated cells in a dose-dependent manner”
Quote in the paperSubstantial claim - Findingown data
Collagen fibers of mice became less dense and more erratically arranged after UVB irradiation.
“the collagen fibers of mice became less dense and more erratically arranged after UVB irradiation”
Quote in the paperSubstantial claim - Findingown data
UVB irradiation significantly increased γH2AX expression in hairless mice.
“Furthermore, IHC analysis also showed that UVB irradiation significantly increased γH2AX expression in hairless mice”
Quote in the paperSubstantial claim - Findingown data
Antioxidin-NV shows strong antioxidant activities by scavenging intracellular and mitochondrial ROS accumulation upon ultraviolet radiation.
“It shows strong antioxidant activities by scaveging intracellular and mitochondrial ROS accumulation upon ultraviolet radiation.”
Quote in the paperSubstantial claim - Findingown data
Antioxidin-NV inhibited UVB-induced MAPK and NF-κB signaling pathway.
“In the present study, antioxidin-NV inhibited UVB-induced MAPK and NF-κB signaling pathway.”
Quote in the paperSubstantial claim - Findingown data
Antioxidin-NV directly scavenged free radicals such as ROS and ABTS+.
“In our work, we found that antioxidin-NV directly scavenged free radicals such as ROS and ABTS+.”
Quote in the paperSubstantial claim - Findingown data
Antioxidin-NV significantly decreased UVB-increased IL-6 secretion in vitro and in vivo.
“antioxidin-NV significantly decreased UVB-increased IL-6 secretion in vitro and in vivo”
Quote in the paperSubstantial claim - Findingown data
Antioxidin-NV increased TGF-β1 secretion in vitro and in vivo.
“Our results indicated that antioxidin-NV increased TGF-β1 secretion in vitro and in vivo.”
Quote in the paperSubstantial claim - Premisecitation
The AOPs can rapidly and constantly eliminate the free radicals of ABTS+ and/or DPPH generated by commercial radical initiators in vitro.
“The AOPs can rapidly and constantly eliminate the free radicals of ABTS+ and/or DPPH that generated by the commercial radical initiators in vitro (Yang et al., 2009; Liu et al., 2010; Lu et al., 2010; Yu et al., 2015; Niu et al., 2018; Cao et al., 2019).”
Quote in the paperNot a substantial claim0 of 3 sources checked - Premisecitation
UV radiation causes excessive reactive oxygen species (ROS) formation from UV absorption by non-DNA chromophores in cells.
“UV radiation causes excessive reactive oxygen species (ROS) formation from UV absorption by non-DNA chromophores in cells (Portugal et al., 2007; Rinnerthaler et al., 2015; Baek and Lee, 2016).”
Quote in the paperSubstantial claim0 of 3 sources checked - Interpretationown data
TLR4 is involved in the antioxidin-NV-mediated IL-6 down-regulation in UVB-irradiated HaCaT cells.
“These results suggest that TLR4 is involved in the antioxidin-NV-mediated IL-6 down-regulation in UVB-irradiated HaCaT cells.”
Quote in the paperSubstantial claim - Interpretationown data
UVB irradiation significantly resulted in cell apoptosis in the skin of mice.
“indicating that UVB irradiation significantly resulted in cell apoptosis in the skin of mice”
Quote in the paperSubstantial claim - Interpretationown data
Antioxidin-NV has strong therapeutic effects against UVB-induced damage.
“suggesting the peptide has strong therapeutic effects against UVB-induced damage”
Quote in the paperSubstantial claim - Interpretationcitation
The mechanism of antioxidin-NV differs from that of other agents against skin photoaging by modulating Nrf2-dependent antioxidant responses or oxidative stress.
“This mechanism differs from that of other agents against skin photoaging by modulating the Nrf2-dependent antioxidant responses (Chaiprasongsuk et al., 2019) or oxidative stress (Zhang et al., 2017).”
Quote in the paperNot a substantial claim0 of 2 sources checked - Interpretationreasoning
Antioxidin-NV could prevent the activation of the mitochondrial pathway of apoptosis by scavenging ROS in vitro and in vivo.
“our results showed that antioxidin-NV could prevent the activation of the mitochondrial pathway of apoptosis by scavenging ROS in vitro and in vivo”
Quote in the paperSubstantial claim - Premisecitation
TGF-β is an important cytokine that promotes collagen production.
“Transforming growth factor-β (TGF-β) is an important cytokine that promotes collagen production (Mouw et al., 2014).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Mouw et al., 2014 source
Not checked in the free run.
- Interpretationown data
Antioxidin-NV is beneficial in the prevention of UVB-induced DNA damage in vivo and in vitro.
“our results suggest that antioxidin-NV is beneficial in the prevention of UVB-induced DNA damage in vivo and in vitro”
Quote in the paperSubstantial claim - Interpretationown data
Antioxidin-NV rescued collagen production in hairless mice upon UVB exposure through restoring TGF-β1/Smad2 signaling.
“suggesting that antioxidin-NV rescued collagen production in hairless mice upon UVB exposure through restoring TGF-β1/Smad2 signaling”
- Also stated in: § Discussion · plain
“Therefore, antioxidin-NV rescued collagen production in UVB-irradiated hairless mice by restoring TGF-β1/Smad2 signaling.”
Quote in the paperSubstantial claim- Rests on an assumption: Smad proteins, including Smad2, are essential components of downstream TGF-β signaling.
- Also stated in: § Discussion · plain
- Interpretationown data
The therapeutic efficacy of antioxidin-NV against UVB-induced skin photoaging is due to its unique amino acid sequence.
“indicating that the therapeutic efficacy of antioxidin-NV against UVB-induced skin photoaging is due to its unique amino acid sequence (Figures 3A–C).”
Quote in the paperSubstantial claim - Interpretationown data
Antioxidin-NV could inhibit UVB-induced cell apoptosis in the skin of hairless mice.
“suggesting that it could inhibit UVB-induced cell apoptosis in the skin of hairless mice”
Quote in the paperSubstantial claim - Interpretationreasoning
Antioxidin-NV had low side effects.
“implying antioxidin-NV had low side effects.”
Quote in the paperNot a substantial claim - Interpretationown data
Antioxidin-NV reduced UVB-induced inflammatory response in HaCaT cells and hairless mice by attenuating UVB-activated TLR4/p38/JNK/NF-κB signaling.
“we concluded that antioxidin-NV reduced UVB-induced inflammatory response in HaCaT cells and hairless mice by attenuating UVB-activated TLR4/p38/JNK/NF-κB signaling”
Quote in the paperSubstantial claim - Premisenone given
Previous studies did not investigate whether these peptides have anti-photoaging activity.
“the previous studies did not investigate whether these peptides have anti-photoaging activity”
Quote in the paperSubstantial claim0 of 2 sources checked - Interpretationreasoning
Antioxidin-NV further decreased the epidermal hyperproliferative response to UVB.
“then further decreased the epidermal hyperproliferative response to UVB”
Quote in the paperSubstantial claim - Interpretationreasoning
Type I collagen rescued by antioxidin-NV is critical for maintaining the elasticity of skin upon UVB irradiation.
“type I collagen rescued by antioxidin-NV is critical for maintaining the elasticity of skin upon UVB irradiation”
Quote in the paperSubstantial claim - Interpretationown data
JNK, p38, IkBa, and NF-κB p65 signaling pathways were involved in antioxidin-NV-mediated downregulation of inflammatory cytokine production upon UVB irradiation.
“This demonstrated that JNK, p38, IkBa, and NF-κB p65 signaling pathways were involved in antioxidin-NV-mediated downregulation of inflammatory cytokine production upon UVB irradiation”
Quote in the paperSubstantial claim - Interpretationreasoning
It is feasible to identify effective anti-photoaging peptide from the frogs lived in the southwestern plateau area of China.
“prove the feasibility to identify effective anti-photoaging peptide from the frogs lived this plateau area”
Quote in the paperSubstantial claim- Rests on an assumption: The southwestern plateau area of China possesses long duration of sunshine and strong ultraviolet radiation.
- Rests on an assumption: The naked skin of frogs in the southwestern plateau area of China evolved an effective antioxidant system to scavenge free radicals induced by light radiation.
- Interpretationown data
Antioxidin-NV activated phosphorylation of Smad2 to increase TGF-β1 secretion in vitro and in vivo.
“Antioxidin-NV activated phosphorylation of Smad2 to increase TGF-β1 secretion in vitro and in vivo.”
Quote in the paperSubstantial claim- Rests on an assumption: Smad proteins, including Smad2, are essential components of downstream TGF-β signaling.
- Interpretationreasoning
The therapeutic effect of antioxidin-NV on UV-induced photoaging was mediated through the alleviation of the oxidative stress-induced process of skin photoaging.
“Our results suggest that the therapeutic effect of antioxidant-NV on UV-induced photoaging was mediated through the alleviation of the oxidative stress-induced process of skin photoaging.”
Quote in the paperSubstantial claim - Interpretationown data
Antioxidin-NV inhibited UVB-induced IL-6 expression by blocking TLR4-mediated inflammatory responses.
“These results indicated that antioxidin-NV inhibited UVB-induced IL-6 expression by blocking TLR4-mediated inflammatory responses”
Quote in the paperSubstantial claim
- May combine two claims. 23
- Classified as probably not a substantial claim. 12
- The quote only partly states this claim. 1
May combine two claims.
Findingown dataAntioxidin-NV did not exhibit cytotoxicity and hemolytic activity at an absolutely high concentration.
“Besides, antioxidin-NV did not exhibit cytotoxicity and hemolytic activity at an absolutely high concentration (Supplementary Figure S3)”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe antioxidin-NV precursor is composed of 72 amino acid residues, including a predicted signal peptide (24 amino acid residue), an acidic peptide region (28 amino acid residue) that ends in a typical trypsin-like proteases processing site (-Lys51Arg52-), followed by a mature peptide (20 amino acid).
“It is composed of 72 amino acid residues, including a predicted signal peptide (24 amino acid residue), an acidic peptide region (28 amino acid residue) that ends in a typical trypsin-like proteases processing site (-Lys51Arg52-), followed by a mature peptide (20 amino acid).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataUVB induced fragmentation of DNA in HaCaT cells and accumulation of γH2AX signals in the cells and in vivo.
“We observed that UVB induced fragmentation of DNA in HaCaT cells and accumulation of γH2AX signals in the cells and in vivo”
Quote in the paperSubstantial claimMay combine two claims.
FindingreasoningAntioxidin-NV ameliorated UVB-induced apoptosis and inhibited the expression of apoptosis-specific protein cleaved caspase 3 in HaCaT cells and skin tissues.
“antioxidin-NV ameliorated UVB-induced apoptosis and inhibited the expression of apoptosis-specific protein, cleaved caspase 3 in HaCaT cells and skin tissues”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataMALDI-TOF MS analysis indicated that antioxidin-NV had a measured molecular mass of 1963.70 Da, matching well with the calculated molecular mass of 1963.30 Da.
“MALDI-TOF MS analysis indicated that antioxidin-NV had a measured molecular mass of 1963.70 Da (Supplementary Figure S2), matching well with the calculated molecular mass of 1963.30 Da.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataAt the concentration of 80 μg/ml, antioxidin-NV scavenged 96% ABTS+ within 1 min, and scavenged nearly 99% ABTS+ within 8 min.
“At the concentration of 80 μg/ml, antioxidin-NV scavenged 96% ABTS+ within 1 min, and scavenged nearly 99% ABTS+ within 8 min.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataNo adverse effect on the body weight, general health or behavior of the mice were observed for the topical antioxidin-NV treatment.
“no adverse effect on the body weight, general health or behavior of the mice were observed for the topical antioxidin-NV treatment”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataUVB-irradiation resulted in a reduction of the thickness of epidermal layers, but topical application of antioxidin-NV significantly reversed this reduction.
“H&E staining of the dorsal skin showed that UVB-irradiation resulted in a reduction of the thickness of epidermal layers, but topical application of antioxidin-NV significantly reversed this reduction (Figures 3B,C).”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataThe skin secretions of N. ventripunctata were divided into five fractions after Sephadex G-50 gel filtration.
“As shown in Supplementary Figure S1A, the skin secretions of N. ventripunctata were divided into five fractions after Sephadex G-50 gel filtration.”
Quote in the paperNot a substantial claimMay combine two claims.
FindingreasoningAntioxidin-NV inhibits UVB-induced DNA damage, apoptosis, and inflammation.
“As subsequent results, it inhibits UVB-induced DNA damage, apoptosis, and inflammation.”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationUV irradiation, especially UVB, triggers overproduction of ROS, leading to photo-induced skin damage, skin diseases and even skin cancer.
“UV irradiation, especially UVB, has the twofold effect of regulating the brain and central neuroendocrine system to rebalance the internal environment (Slominski et al., 2018), and triggering the overproduction of ROS, leading to photo-induced skin damage, skin diseases and even skin cancer (Rinnerthaler et al., 2015).”
Quote in the paperSubstantial claim0 of 2 sources checkedMay combine two claims.
PremisecitationThe two frog-skin AOPs antioxidin-RL and OA-VI12 prevented UVB irradiation-induced photoaging in mice, but their detailed mechanisms remain to be fully understood.
“They prevented UVB irradiation-induced photoaging in mice, but the detailed mechanisms of the two AOPs remain to be fully understood.”
Quote in the paperSubstantial claim0 of 2 sources checkedMay combine two claims.
PremisecitationFrog-skin antioxidant peptides (AOPs) possess gene-encoded origins like antioxidant enzymes but show no enzyme activity, and instead function as direct free radical scavengers like low molecular weight antioxidants (LMWAs).
“They possess gene-encoded origins as antioxidant enzymes do, but they show no enzyme activity. Instead they function as direct free radical scavengers like LMWAs.”
Quote in the paperSubstantial claim0 of 2 sources checkedMay combine two claims.
Interpretationown dataAntioxidin-NV directly and rapidly scavenged excessive ROS upon UVB irradiation, subsequently alleviated UVB-induced DNA damage, cell apoptosis, and inflammatory response, thus protecting against UVB-induced skin photoaging.
“Taken together, antioxidin-NV directly and rapidly scavenged excessive ROS upon UVB irradiation, subsequently alleviated UVB-induced DNA damage, cell apoptosis, and inflammatory response, thus protecting against UVB-induced skin photoaging.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationCurrently, only two frog-skin AOPs with potential skin protective effects in vivo have been described.
“Currently, only two frog-skin AOPs with potential skin protective effects in vivo have been described (Qin et al., 2018; Yin et al., 2019).”
Quote in the paperNot a substantial claim0 of 2 sources checkedClassified as probably not a substantial claim. May combine two claims.
PremisecitationThe overproduction and/or mismanagement of ROS may result in oxidative stress, which has been implicated in a large variety of skin disorders and skin diseases, such as UV irradiation damages, skin inflammation, bacterial skin infections, and skin cancer.
“The overproduction and/or mismanagement of ROS may result in oxidative stress, which have been implicated in a large variety of skin disorders and skin diseases, such as UV irradiation damages, skin inflammation, bacterial skin infections, and skin cancer (Portugal et al., 2007; Pham-Huy et al., 2008; Godic et al., 2014).”
Quote in the paperSubstantial claim0 of 3 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenResults are shown as mean ± SD from three independent experiments.
“Results are shown as mean ± SD from three independent experiments.”
Quote in the paperNot a substantial claimMay combine two claims.
Interpretationown dataThe data indicate that antioxidin-NV had a strong ability to scavenge ROS induced by UVB irradiation, suggesting a strong antioxidant activity of antioxidin-NV.
“The data indicate that antioxidin-NV had a strong ability to scavenge ROS induced by UVB irradiation, suggesting a strong antioxidant activity of antioxidin-NV.”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationHSFs can synthesize and maintain the extracellular matrix of skin and reduce skin photoaging.
“HSFs, which can synthesize and maintain the extracellular matrix of skin and reduce skin photoaging, are a very critical cell type in skin photoaging (Tobin, 2017).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Tobin, 2017 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationCollagen is derived from HSF cells and plays an important role in maintaining the elasticity of skin.
“Collagen is derived from HSF cells and plays important role in maintaining the elasticity of skin (Lee et al., 2012).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Lee et al., 2012 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationType I collagen is the major component of collagen fibrils and the most abundant structural protein in the skin.
“Type I collagen, which is the major component of collagen fibrils, is the most abundant structural protein in the skin (Makrantonaki and Zouboulis, 2007).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Makrantonaki and Zouboulis, 2007
Not checked in the free run.
Classified as probably not a substantial claim.
InterpretationreasoningTo cope with the increasing oxidative stress, N. ventripunctata should possess potent free radical scavenging and radio-protective effect for their survival.
“To cope with the increasing oxidative stress, N. ventripunctata should possess potent free radical scavenging and radio-protective effect for their survival.”
Quote in the paperSubstantial claim- Rests on an assumption: N. ventripunctata lives in high altitude (3120–4100 m) where there is low temperature, long sunshine duration and strong ultraviolet radiation.
Classified as probably not a substantial claim.
PremisecitationMAPKs and NF-κB signaling are important signal transduction pathways activated by UVB irradiation.
“MAPKs and NF-κB signaling are known to be important signal transduction pathways activated by UVB irradiation (Subedi et al., 2017).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Subedi et al., 2017 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationThe TGF-β/Smad pathway promotes the differentiation of myofibroblasts.
“the TGF-β/Smad pathway also promotes the differentiation of myofibroblasts (Guo et al., 2009).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Guo et al., 2009 source
Not checked in the free run.
May combine two claims.
Premisecitationα-SMA is a marker of myofibroblast which has a higher capacity to synthesize collagen.
“a-SMA is also a marker of myofibroblast which has a higher capacity to synthesize collagen (Nakyai et al., 2018).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Nakyai et al., 2018 source
Not checked in the free run.
May combine two claims.
PremisecitationInflammation enhances the epidermal hyperproliferative response to UVB and plays a crucial role in promoting skin photoaging.
“Inflammation was found to enhance the epidermal hyperproliferative response to UVB and play a crucial role in promoting skin photoaging (Pillai et al., 2005).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Pillai et al., 2005 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). The quote only partly states this claim.
Study design and conductnone givenHistological and immunohistochemical slides were read in blindness.
“The pathology slides were read in blindness, and the images were recorded.”
- Also stated in: § Masson Stain · plain
“Finally, the slides were read in blindness, and the images were recorded.”
Quote in the paperNot a substantial claim- Also stated in: § Masson Stain · plain
Classified as probably not a substantial claim.
Study design and conductnone givenThe mice were randomized into five treatment groups (six mice per group).
“The mice were randomized into five treatment groups (six mice per group)”
Quote in the paperSubstantial claimMay combine two claims.
Interpretationown dataAntioxidin-NV identified from N. ventripunctata skin is a bioactive/effector compound with potential anti-photoaging ability.
“antioxidin-NV identified from N. ventripunctata skin is a bioactive/effector compound with potential anti-photoaging ability”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationSeries of peptides have been identified with antioxidant activity from the skin of frogs lived in this plateau area.
“series of peptides have been identified with antioxidant activity from the skin of frogs lived in this plateau area (Yang et al., 2009; Liu et al., 2010)”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
Interpretationown dataThese pathways may orchestrate in regulating cytokine expression and inhibiting skin photoaging process.
“they may orchestrate in regulating these cytokines expression and inhibiting skin photoaging process”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationreasoningAntioxidin-NV-mediated reduction of free radical accumulation led to the reduction of DNA damage, apoptosis, and inflammation upon UVB radiation, thereby providing protection against UVB-induced skin photoaging.
“antioxidin-NV-mediated reduction of free radical accumulation led to the reduction of DNA damage, apoptosis, and inflammation upon UVB radiation, thereby providing protection against UVB-induced skin pohto-aging”
Quote in the paperSubstantial claim
The paper relies on this without support.
N. ventripunctata lives in high altitude (3120–4100 m) where there is low temperature, long sunshine duration and strong ultraviolet radiation.
“N. ventripunctata lives in high altitude (3120–4100 m) where there is low temperature, long sunshine duration and strong ultraviolet radiation.”
The paper relies on this without support.
Smad proteins, including Smad2, are essential components of downstream TGF-β signaling.
“Smad proteins, including Smad2, are essential components of downstream TGF-β signaling.”
“Smad proteins, including Smad2, are key regulators in TGF-β signaling pathways and they are essential components of downstream TGF-β signaling.”
The paper relies on this without support.
The southwestern plateau area of China possesses long duration of sunshine and strong ultraviolet radiation.
“This plateau area possesses long duration of sunshine, and suffers strong ultraviolet radiation”
The paper relies on this without support.
The naked skin of frogs in the southwestern plateau area of China evolved an effective antioxidant system to scavenge free radicals induced by light radiation.
“which make the naked skin of frogs evolve an effective antioxidant system to scavenge free radicals induced by light radiation”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
A cathelicidin molecule from the spot-bellied plateau frog Nanorana ventripunctata has been shown to reduce the effects of ultraviolet B on skin photoaging in mice by ROS scavenging.
“Recently, a cathelicidin molecule (ARGKKECKDDRCRLLMKRGSFSYV) from the spot-bellied plateau frog Nanorana ventripunctata has been shown to reduce the effects of ultraviolet B (UVB) on skin photoaging in mice by ROS scavenging [189].”
From The Role of Reactive Species on Innate Immunity (2022) · cites this paper as [189]
Antimicrobial peptides are involved in the regulation of oxidative-antioxidant homeostasis.
“This could lead to the notion that antimicrobial peptides are involved in the regulation of oxidative-antioxidant homeostasis.”
From The Role of Reactive Species on Innate Immunity (2022) · cites this paper as [189]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Opposite effects reported for epidermal thickness
MajorThe Results say UVB reduced epidermal thickness and antioxidin-NV reversed that reduction. The Figure 3 caption instead says antioxidin-NV decreased UVB-induced thickness, reversing the direction of a reported treatment effect.
“H&E staining of the dorsal skin showed that UVB-irradiation resulted in a reduction of the thickness of epidermal layers, but topical application of antioxidin-NV significantly reversed this reduction (Figures 3B,C).”
“Topical application of antioxidin-NV significantly suppressed UVB-induced skin photoaging in hairless mice, obviously decreased skin erythema, thickness and wrinkle formation.”
Conflicting DCFH-DA concentrations
MajorThe method specifies 30 μM DCFH-DA for the cellular ROS assay, whereas the Figure 2 caption specifies 10 μM for the HaCaT-cell measurement.
“cells were stained with 30 μM 2′, 7′- DCFH-DA (Sigma, United States) for 30 min at 37°C in a CO2 incubator.”
“DCFH-DA (10 μM) was introduced into HaCaT cells, and fluorescence was measured by flow cytometry.”
Different cell types named for TGF-β1 result
MinorThe Results attribute the dose-dependent TGF-β1 increase to HSF cells, but the Discussion attributes it to HaCaT cells.
“antioxidin-NV treatment significantly increased TGF-β1 production in UVB-irradiated HSF compared with PBS treatment in a dose-dependent manner (Figures 10A,B).”
“Antioxidin-NV significantly increased UVB-inhibited TGF-β1 secretion in a dose-dependent manner in HaCaT cells.”
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The Role of Reactive Species on Innate Immunity
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- Authors
- Feng, G., Wei, L., Che, H., Shen, Y., Yang, J., Mi, K., Liu, J., Wu, J., Yang, H., & Mu, L.
- Affiliations
- Kunming Medical University (CN)
- Soochow University (CN)
- Chinese People's Liberation Army (CN)
- Corresponding author
- Wu, Jing
- Yang, Hailong
- Mu, Lixian
- Venue
- Frontiers in Pharmacology
- Publisher
- Frontiers Media SA
- Published
- 2022-01-19
- Volume
- 12
- Pages
- 761011-761011
- ISSN
- 1663-9812 (ISSN-L)
- PMC
- PMC8807480
- OpenAlex
- W4206681594
- Semantic Scholar
- 145d6405f9d5dafd89f6e099478d641e1dccd28e
- Cited by
- 30
- References
- 46
- Citations by year
- 2026: 7 · 2025: 8 · 2024: 11 · 2023: 2 · 2022: 2
- FWCI
- 5.62
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Frontiers in Pharmacology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Natural Science Foundation of Yunnan Province (202101AY070001-004, 2019HB023, 81673401, 82160680, 81560581, 2018FE001(-135)
- Priority Academic Program Development of Jiangsu Higher Education Institutions
- Topics
- Health Sciences › Medicine › Dermatology › Skin Protection and Aging
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › melanin and skin pigmentation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Hydrolysis and Bioactive Peptides
- Keywords
- photoaging, frog skin peptides, antioxidant peptides, reactive oxygen species scavenging, DNA damage, apoptosis, interleukin-6, TLR4 signaling, NF-κB signaling, TGF-β1/Smad2 signaling, collagen synthesis, keratinocytes, dermal fibroblasts
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Claims read by deepseek-v4.1-flash under definition version 3 (extract-v3) on 2026-10-06.
Classified by jev-1.13-20260917 (gold-guideline-v0.2) on 2026-10-06.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
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