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Subchronic toxicity study of Coptidis Rhizoma in rats
Authors:Yong-Hoon Lee  Duyeol Kim  Mi Ju Lee  Myoung Jun Kim  Ho-Song Jang  Sun Hee Park  Jung-Min Lee  Hye-Yeong Lee  Beom Seok Han  Woo-Chan Son  Ji Hyeon Seok  Jong Kwon Lee  Jayoung Jeong  Jin Seok Kang  Jong-Koo Kang
Institution:1. Department of Pathology, Biotoxtech Co., Ltd, 686-2 Yangcheong-ri, Ochang-eup, Cheongwon-gun 363-883, Chungbuk, Republic of Korea;2. Division of Toxicopathology, Hoseo Toxicology Research Center, Hoseo University, 79 Hoseo-ro, BaeBang-Myeon, Asan 336-795, Chungnam, Republic of Korea;3. Department of Pathology, University of Ulsan College of Medicine, Asan Medical Center, 88 Olympic-ro 43-gil, Songpa-gu, Seoul 138-736, Republic of Korea;4. Toxicological Research Divison, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Osong Health Technology Administration Complex, 187 Osongsaengmyeong2-ro, Osong, Cheongwon 363-700, Chungbuk, Republic of Korea;5. Department of Biomedical Laboratory Science, Namseoul University, 21 Maeju-ri, Seonghwan-eup, Cheonan 331-707, Chungnam, Republic of Korea;6. Department of Laboratory Animal Medicine, College of Veterinary Medicine, Chungbuk National University, 410 Naesudong-ro, Heungdeok-gu, Cheongju 361-763, Chungbuk, Republic of Korea
Abstract:

Ethnopharmacological relevance

Coptidis Rhizoma (CR) is a medical herb from the family Ranunculacease that has been used to treat gastroenteritis, dysentery, diabetes mellitus, and severe skin diseases.

Aim of the study

To evaluate the no-observed-adverse-effect level (NOAEL) and the toxicity of CR, following repeat oral administration to rats for 13 weeks.

Materials and methods

CR was administered by oral gavage to groups of rats (n=10/group, each sex) at dose levels of 0 (control), 25, 74, 222, 667 or 2000 mg/kg/day 5 times per week for 13 weeks. Mortality, clinical signs, body weights, food consumption, hematology, serum chemistry, urinalysis, vaginal cytology and sperm morphology, organ weights, gross and histopathological findings were compared between control and CR groups.

Results

Urinalysis showed a significant increase in N-acety1-β-glucosaminidase in males in the 2000 mg/kg/day group (P<0.01). However, no mortality or remarkable clinical signs were observed during this 13-week study. No adverse effects on body weight, food consumption, hematology, serum chemistry, organ weights, gross lesion, histopathology, vaginal cytology, sperm motility, or deformity were observed in the males or female rats treated with CR.

Conclusions

On the basis of these results, the NOAEL of CR is determined to be 667 mg/kg/day for males and 2000 mg/kg/day for females.
Keywords:ANOVA  analysis of variance  CR  Coptidis Rhizoma  NOAEL  no-observed-adverse-effect level  NTP  National Toxicology Program  GLP  good laboratory practice  MFDS  Ministry of Food and Drug Safety  HPLC  high performance liquid chromatography  NAG  N-acetyl-β-glucosaminidase  CRE  creatinine  AST  aspartate aminotransferase  ALP  alkaline phosphatase  GGT  gamma-glutamyl transpeptidase  RBC  total erythrocyte counts  HGB  hemoglobin concentration  HCT  hematocrit  MCV  mean cell volume  MCH  mean cell hemoglobin  MCHC  mean cell hemoglobin concentration  PLT  platelet count  RBC  total leukocyte counts  NEU  neutrophils  EOS  eosinophils  Baso  basophils  Lym  lymphocytes  MONO  monocytes  RET  reticulocytes  PT  prothrombin time  APTT  activated partial thromboplastin time  ALT  alanine aminotransferase  AST  aspartate aminotransferase  ALP  alkaline phosphatase  SDH  sorbitol dehydrogenase  BUN  blood urea nitrogen  T-BIL  total bilirubin  TP  total protein  ALB  albumin  A/G  albumin/globulin  T-CHO  total cholesterol  TG  triglycerides  GLU  glucose  Ca  calcium  Cl  chloride  Na  sodium  K  potassium
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