1.The in vivo rodent micronucleus assay of Kacip Fatimah (Labisia pumila) extract.
Shahrim Zaizuhana ; M B Puteri J Noor ; Yahya Noral'ashikin ; Hussin Muhammad ; A B Rohana ; I Zakiah
Tropical biomedicine 2006;23(2):214-9
Kacip Fatimah also known as Labisia pumila (Myrsinaceae), is a traditional herbal medicine with a long history in the Malay community. It has been used by many generations of Malay women to induce and facilitate childbirth as well as a post-partum medicine. We tested the genotoxic potential of Kacip Fatimah in bone marrow cells obtained from Sprague-Dawley rats using micronuclei formation as the toxicological endpoints. Five groups of five male rats each were administered orally for two consecutive days with doses of 100, 700 and 2000 mg/kg body weight of Kacip Fatimah extract dissolved in distilled water. Micronucleus preparation was obtained from bone marrow cells of the animals following standard protocols. No statistically significant increase in micronucleated polychromatic erythrocytes (MNPCEs) was observed at any dose level and sacrifice/harvest time point (24, 48 and 72h). However, a significant decrease in polychromatic erythrocytes/normochromatic erythrocytes (PCE:NCE) ratio was observed from the highest dose level (2000 mg/kg of body weight) at 48h harvest time point. In this study, we investigated the effect of Kacip Fatimah on mammalian bone marrow cells using micronuclei formation to assess the genotoxicity of the herb.
Micronuclei
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Erythrocytes
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Bone Marrow
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in vivo
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assay
2.Classical natural ovine scrapie prions detected in practical volumes of blood by lamb and transgenic mouse bioassays.
Rohana P DASSANAYAKE ; Thomas C TRUSCOTT ; Dongyue ZHUANG ; David A SCHNEIDER ; Sally A MADSEN-BOUTERSE ; Alan J YOUNG ; James B STANTON ; William C DAVIS ; Katherine I O'ROURKE
Journal of Veterinary Science 2015;16(2):179-186
Scrapie is diagnosed antemortem in sheep by detecting misfolded isoforms of prion protein (PrP(Sc)) in lymphoid follicles of the rectal mucosa and nictitating membranes. Assay sensitivity is limited if (a) the biopsy is collected early during disease development, (b) an insufficient number of follicles is collected, or (c) peripheral accumulation of PrP(Sc) is reduced or delayed. A blood test would be convenient for mass live animal scrapie testing. Currently approved techniques, however, have their own detection limits. Novel detection methods may soon offer a non-animal-based, rapid platform with detection sensitivities that rival the prion bioassay. In anticipation, we sought to determine if diseased animals could be routinely identified with a bioassay using B lymphocytes isolated from blood sample volumes commonly collected for diagnostic purposes in small ruminants. Scrapie transmission was detected in five of six recipient lambs intravenously transfused with B lymphocytes isolated from 5~10 mL of blood from a naturally scrapie-infected sheep. Additionally, scrapie transmission was observed in 18 ovinized transgenic Tg338 mice intracerebrally inoculated with B lymphocytes isolated from 5~10 mL of blood from two naturally scrapie-infected sheep. Based on our findings, we anticipate that these blood sample volumes should be of diagnostic value.
Animals
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B-Lymphocytes/*pathology
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Biological Assay/*veterinary
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Mice
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Mice, Transgenic
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Prions/*blood
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Scrapie/blood/*diagnosis/transmission
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Sheep