TY - JOUR
T1 - Assessing therapeutic efficacy of Chlorella vulgaris peptides on pathogenic bacteria associated with periodontal disease
AU - Wang, Shu Mei
AU - Chang, Chia Yu
AU - Chuu, Jiunn Jye
AU - Lee, Ching Kuo
N1 - Publisher Copyright:
© 2025 The Author(s). Published with license by Taylor & Francis Group, LLC.
PY - 2025
Y1 - 2025
N2 - Periodontal diseases (PD) adversely impact periodontium caused by infectious bacteria. Recently, Chlorella species have been recognized for their preventive potential against various diseases. Therefore, we aimed to elucidate pharmacological activity of Chlorella vulgaris peptides (CVP, molecular weights of <1 kDa, 1–3 kDa, 3–10 kDa, 10–30 kDa and >30 kDa) for bacterial-associated periodontal disorders. We investigated anti-bacterial, anti-inflammatory profile, cell protection, and anti-osteoclastogenic profiles on Streptococcus mutans, Streptococcus sanguis, Porphyromonas gingivalis. The CVP 3–10 kDa and 10–30 kDa inhibited bacterial growth, elevated SCC-4 and RAW264.7 cell survival rate under LPS-treatment and reduced osteoclast numbers. In vivo study revealed significantly reduced oral bacterial count and MCP-1 in CVP 3–10 kDa gel-treated LPS+bacteria-induced mice, possibly by regulating TLR4 signaling and inhibiting inflammatory cytokines such as IL-6 and TNF-α. Conclusively, CVPs exert anti-bacterial, anti-inflammatory, cell protective, wound healing, and anti-osteoclastogenic activities and therefore could be a potential therapy for PDs.
AB - Periodontal diseases (PD) adversely impact periodontium caused by infectious bacteria. Recently, Chlorella species have been recognized for their preventive potential against various diseases. Therefore, we aimed to elucidate pharmacological activity of Chlorella vulgaris peptides (CVP, molecular weights of <1 kDa, 1–3 kDa, 3–10 kDa, 10–30 kDa and >30 kDa) for bacterial-associated periodontal disorders. We investigated anti-bacterial, anti-inflammatory profile, cell protection, and anti-osteoclastogenic profiles on Streptococcus mutans, Streptococcus sanguis, Porphyromonas gingivalis. The CVP 3–10 kDa and 10–30 kDa inhibited bacterial growth, elevated SCC-4 and RAW264.7 cell survival rate under LPS-treatment and reduced osteoclast numbers. In vivo study revealed significantly reduced oral bacterial count and MCP-1 in CVP 3–10 kDa gel-treated LPS+bacteria-induced mice, possibly by regulating TLR4 signaling and inhibiting inflammatory cytokines such as IL-6 and TNF-α. Conclusively, CVPs exert anti-bacterial, anti-inflammatory, cell protective, wound healing, and anti-osteoclastogenic activities and therefore could be a potential therapy for PDs.
KW - anti-bacterial
KW - anti-inflammation
KW - anti-osteoclastogenic
KW - biofilm
KW - chlorella vulgaris
KW - Periodontal diseases
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U2 - 10.1080/19476337.2025.2471783
DO - 10.1080/19476337.2025.2471783
M3 - Article
AN - SCOPUS:105000697598
SN - 1947-6337
VL - 23
JO - CYTA - Journal of Food
JF - CYTA - Journal of Food
IS - 1
M1 - 2471783
ER -