Protective effects of pine bark extract on developmental toxicity of cyclophosphamide in rats

Sung Hwan Kim, In Chul Lee, Jeong Hyeon Lim, Changjong Moon, Chun Sik Bae, Sung Ho Kim, Dong Ho Shin, Seung Chun Park, Hyoung Chin Kim, Jong Choon Kim

Research output: Contribution to journalArticlepeer-review

30 Scopus citations

Abstract

This study investigated the protective effects of pine bark extract (Pycnogenol®, PYC) against cyclophosphamide (CP)-induced developmental toxicity in rats. A total of 44 mated females were randomly assigned to the following four experimental groups: (1) vehicle control, (2) CP, (3) CP&PYC, or (4) PYC. All dams were subjected to a Caesarean section on day 20 of gestation, and fetuses were examined for morphological abnormalities. Oxidative stress analysis was performed on maternal hepatic tissues. CP treatment caused decreased fetal and placental weights and increased embryonic resorptions and fetal malformations. In addition, an increased malondialdehyde (MDA) concentration and decreased reduced glutathione (GSH) content and catalase activity were observed in the hepatic tissues. On the contrary, PYC treatment during pregnancy significantly ameliorated the CP-induced embryo-fetal developmental toxicity in rats. Moreover, MDA and GSH concentrations and catalase activity in hepatic tissues were not affected when PYC was administered in conjunction with CP. These results suggest that repeated administration of PYC has beneficial effects against CP-induced embryo-fetal developmental toxicity in rats, and that the protective effects of PYC may be due to both inhibition of lipid peroxidation and increased antioxidant activity.

Original languageEnglish
Pages (from-to)109-115
Number of pages7
JournalFood and Chemical Toxicology
Volume50
Issue number2
DOIs
StatePublished - Feb 2012

Keywords

  • Cyclophosphamide
  • Developmental toxicity
  • Oxidative stress
  • Protective effects
  • Pycnogenol®

Fingerprint

Dive into the research topics of 'Protective effects of pine bark extract on developmental toxicity of cyclophosphamide in rats'. Together they form a unique fingerprint.

Cite this