The Osmanthus fragrans flower phenylethanoid glycoside-rich extract: Acute and subchronic toxicity studies. (1st July 2016)
- Record Type:
- Journal Article
- Title:
- The Osmanthus fragrans flower phenylethanoid glycoside-rich extract: Acute and subchronic toxicity studies. (1st July 2016)
- Main Title:
- The Osmanthus fragrans flower phenylethanoid glycoside-rich extract: Acute and subchronic toxicity studies
- Authors:
- Lu, Baiyi
Li, Maiquan
Zhou, Fei
Huang, Weisu
Jiang, Yirong
Mao, Shuqin
Zhao, Yajing
Lou, Tiantian - Abstract:
- Abstract: Ethnopharmacological relevance: Osmanthus fragrans var. thunbergii ( O. fragrans ) flower has been consumed as folk medicine for thousands of years. O. fragrans flower extract is a well-characterized phenylethanoid glycoside-rich extract, which has been used as a natural anti-oxidant. The aim of this study was to evaluate the safety of O. fragrans flower phenylethanoid glycoside-rich extract (OFFE). Materials and methods: The OFFE was extracted by 80% (v/v) aqueous ethanol with 0.01% sodium isoascorbate (w/v) from the O. fragrans flower and purified on HPD300 resins. The total phenylethanoid glycosides content and individual phenylethanoid glycosides was determined by photocolorimetric method and reversed phase UPLC respectively. An acute oral toxicity study, reverse mutation test, bone marrow cell micronucleus test, and sperm abnormality test as well as a 90-day oral toxicity study were performed on experimental animals. Results: The total content of phenylethanoid glycosides in OFFE was 73.4 g acteoside equivalent per 100 g of extract, include acteoside (52.5 g per 100 g of extract), salidroside (13.8 g per 100 g of extract), and isoacteoside (2.6 g per 100 g of extract) and so on. No acute lethal effect at the maximal tested OFFE dose of 10 g/kg body weight (bw) in either rats or mice was observed, suggesting that OFFE can be considered nontoxic. No evidence for mutagenicity was detected in any of the three mutagenic tests. Administration at levels of 0.50,Abstract: Ethnopharmacological relevance: Osmanthus fragrans var. thunbergii ( O. fragrans ) flower has been consumed as folk medicine for thousands of years. O. fragrans flower extract is a well-characterized phenylethanoid glycoside-rich extract, which has been used as a natural anti-oxidant. The aim of this study was to evaluate the safety of O. fragrans flower phenylethanoid glycoside-rich extract (OFFE). Materials and methods: The OFFE was extracted by 80% (v/v) aqueous ethanol with 0.01% sodium isoascorbate (w/v) from the O. fragrans flower and purified on HPD300 resins. The total phenylethanoid glycosides content and individual phenylethanoid glycosides was determined by photocolorimetric method and reversed phase UPLC respectively. An acute oral toxicity study, reverse mutation test, bone marrow cell micronucleus test, and sperm abnormality test as well as a 90-day oral toxicity study were performed on experimental animals. Results: The total content of phenylethanoid glycosides in OFFE was 73.4 g acteoside equivalent per 100 g of extract, include acteoside (52.5 g per 100 g of extract), salidroside (13.8 g per 100 g of extract), and isoacteoside (2.6 g per 100 g of extract) and so on. No acute lethal effect at the maximal tested OFFE dose of 10 g/kg body weight (bw) in either rats or mice was observed, suggesting that OFFE can be considered nontoxic. No evidence for mutagenicity was detected in any of the three mutagenic tests. Administration at levels of 0.50, 1.00, and 2.00 g/kg bw to rats for 90 days failed to induce any significant hematological, clinical, chemical, or histopathological changes. The no-observed adverse-effect-level for OFFE was >2.00 g/kg bw for the study on subchronic toxicity. Conclusion: The results showed that consuming OFFE has no adverse effects and poses no health risk in the acute oral toxicity study, subchronic oral toxicity study, and in the micronucleus test, which may provide supportive evidence for the safety of OFFE powder that has been used in medicine as well as in functional foods, and dietary supplements. Graphical abstract: … (more)
- Is Part Of:
- Journal of ethnopharmacology. Volume 187(2016)
- Journal:
- Journal of ethnopharmacology
- Issue:
- Volume 187(2016)
- Issue Display:
- Volume 187, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 187
- Issue:
- 2016
- Issue Sort Value:
- 2016-0187-2016-0000
- Page Start:
- 205
- Page End:
- 212
- Publication Date:
- 2016-07-01
- Subjects:
- Ab albumin -- ALT alanine aminotransferase -- AST aspartate aminotransferase -- BUN blood urea nitrogen -- CN creatinine -- CPA cyclophosphamide -- FSA frequencies of sperm abnormalities -- Gb globulin -- GLC granular leukocyte count -- Glu glucose -- Hb hemoglobin -- LLC lymph leukocyte count -- MLC mononuclear leukocyte count -- MMC mitomycin C -- MN frequencies of micronucleus -- MNRETs micronuclei peripheral reticulocytes -- MTD the maximum tolerated dose -- OFEE 75% ethanol extraction of Osmanthus fragrans -- OFFE Osmanthus fragrans flower phenylethanoid glycoside-rich extract -- PCE polychromatic erythrocytes -- RBC red blood cell -- TC total cholesterol -- TG triglycerides -- TP total protein -- WBC total leukocyte count
Acteoside (PubChem CID: 354009) -- Salidroside (PubChem CID: 159278) -- Isoacteoside (PubChem CID: 6438553) -- Chlorogenic acid (PubChem CID: 1794427) -- Caffeic acid (PubChem CID: 689043)
OFFE -- Phenylethanoid glycoside -- Acteoside -- Acute toxicity sudy -- Subchronic toxicity study -- Nontoxic
Ethnopharmacology -- Periodicals
Pharmacognosy -- Periodicals
Herbs -- Periodicals
Herbs -- Periodicals
Pharmacognosy -- Periodicals
Pharmacognosie -- Périodiques
Herbes -- Périodiques
615.1 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03788741 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.jep.2016.04.049 ↗
- Languages:
- English
- ISSNs:
- 0378-8741
- Deposit Type:
- Legaldeposit
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- British Library DSC - 4979.602400
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