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Sea Cucumber Viscera Contains Novel Non-Holostane-Type Glycoside Toxins that Possess a Putative Chemical Defense Function.
Liu, Yanfang; Lu, Zhen; Yan, Zhi; Lin, Ainuo; Han, Shaoshuai; Li, Yaxi; Yang, Xiao; Li, Xiaodong; Yin, Xiuli; Zhang, Ranran; Li, Ke.
Afiliación
  • Liu Y; Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai, 264003, China.
  • Lu Z; College of Resources and Environment, University of Chinese Academy of Sciences, Beijing, 100049, China.
  • Yan Z; Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai, 264003, China.
  • Lin A; Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai, 264003, China.
  • Han S; School of Ocean, Yantai University, Yantai, 264005, China.
  • Li Y; Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai, 264003, China.
  • Yang X; College of Resources and Environment, University of Chinese Academy of Sciences, Beijing, 100049, China.
  • Li X; Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai, 264003, China.
  • Yin X; School of Marine Science and Technology, Harbin Institute of Technology, Weihai, 264209, China.
  • Zhang R; Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai, 264003, China.
  • Li K; College of Resources and Environment, University of Chinese Academy of Sciences, Beijing, 100049, China.
J Chem Ecol ; 50(3-4): 185-196, 2024 Apr.
Article en En | MEDLINE | ID: mdl-38441803
ABSTRACT
Sea cucumbers frequently expel their guts in response to predators and an aversive environment, a behavior perceived as releasing repellents involved in chemical defense mechanisms. To investigate the chemical nature of the repellent, the viscera of stressed sea cucumbers (Apostichopus japonicus) in the Yellow Sea of China were collected and chemically analyzed. Two novel non-holostane triterpene glycosides were isolated, and the chemical structures were elucidated as 3ꞵ-O-[ꞵ-D-glucopyranosyl-(1→2)-ꞵ-D-xylopyranosyl]-(20S)-hydroxylanosta-7,25-diene-18(16)-lactone (1) and 3ꞵ-O-[ꞵ-D-quinovopyranosyl-(1→2)-ꞵ-D-xylopyranosyl]-(20S)-hydroxylanosta-7,25-diene-18(16)-lactone (2) by spectroscopic and mass-spectrometric analyses, exemplifying a triterpene glycoside constituent of an oligosaccharide containing two sugar-units and a non-holostane aglycone. Zebrafish embryos were exposed to various doses of 1 and 2 from 4 to 96 hpf. Compound 1 exposure showed 96 h-LC50 41.5 µM and an increased zebrafish mortality rates in roughly in a dose- and time-dependent manner. Compound 2, with different sugar substitution, exhibited no mortality and moderate teratogenic toxicity with a 96 h-EC50 of 173.5 µM. Zebrafish embryos exhibited teratogenic effects, such as reduced hatchability and total body length. The study found that triterpene saponin from A. japonicus viscera had acute toxicity in zebrafish embryos, indicating a potential chemical defense role in the marine ecosystem.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Pepinos de Mar / Triterpenos / Vísceras / Pez Cebra / Glicósidos Límite: Animals Idioma: En Revista: J Chem Ecol Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Pepinos de Mar / Triterpenos / Vísceras / Pez Cebra / Glicósidos Límite: Animals Idioma: En Revista: J Chem Ecol Año: 2024 Tipo del documento: Article País de afiliación: China