• 생약학회지
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• 제22권3호
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• pp.197-206
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• 1991

The water extract of Gamisamryungbaekchool-San increased the lifespan of mice implanted intraperitoneally with sarcoma 180. Significant depression of lethal toxicity of cis-platin $(45{\mu}M/kg,\;s.c)$ and renal toxicity (indicated by an increase in blood urea nitrogen value and creatinine value) of cis-platin $(35{\mu}M/kg,\;s.c)$ were observed in mice and rats treated with Gamisamryungbaekchool-San. RBC and WBC were significantly decreased in rats treated with cis-platin, and significant depression of hematologic toxicities of cis-platin $(35{\mu}M/kg,\;s.c)$ in rats treated with Gamisamryungbaekchool-San. After all, alleviative effect of the side actions of cis-platin was acknowledged by combined usage of Gamisamryungbaekchool-San and cis-platin.

• 생약학회지
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• 제23권2호
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• pp.89-95
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• 1992

The water extract of Gamidaebo-Tang depressed the lethal toxicity of cis-platin$(45{\mu}M/kg,\;s.c.)$, and mitomycin C (6mg/kg, s.c.). Significant depression of renal toxicity(indicated by an increased blood urea nitrogen value and creatinine value) of cis-platin $(35{\mu}M/kg)\;s.c.)$, was observed in mice treated with Gamidaebo-Tang. In rats treated with mitomycin C and Gamidaebo-Tang, the increased LDH activity and reduced total protein and albumin contents by mitomycin C were significantly depressed. The number of WBC was significantly increased in rats treated with mitomycin C but in the rats treated with mitomycin C and Gamidaebo-Tang, the number of WBC was increased and the hematocrit value and the number of RBC and Hgb were significantly increased in the dose-dependent manner. Therefore, bone marrow toxicity of mitomycin C in the rats treated with Gamidaebo-Tang was depressed. In the end, alleviative effects of the side actions of cis-platin and mitomycin C were acknowledged by combined usage of Gamidaebo-Tang and these anti-neoplastic drugs.

• Environmental Analysis Health and Toxicology
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• 제24권4호
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• pp.351-357
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• 2009

To investigate the alleviative effects of jujube water extract (JWE) on the inflammation and skin barrier damage, both the irradiation of UVB and the application of squalene monohydroperoxide (Sq-OOH) were applied to the back skin of experimental animals for 4 weeks. And at the same time experimental materials were applied topically. Six weeks female SKH-1 hairless mice were divided into five groups (five animals for each group) including normal (N; saline), control (C; UVB+Sq-OOH+saline), vehicle control (VC; UVB+Sq-OOH+vehicle), positive control (PC; UVB+Sq-OOH+0.01% retinoic acid) and experimental (E; UVB+Sq-OOH+JWE) groups. The skin erythema index in the E group was significantly low compared to the C group (p<0.05). Lipid (p<0.05) and water (p<0.01) capacities in the E group were significantly high compared to the C group. In comparison with the C group, E group showed a relatively well preserved lipid lamellae in the epidermis and a relatively much less infiltration of mast cells in the dermis or hypodermis. As for the both absolute and relative weights of the spleen, PC group were significantly higher than the other groups. These results suggest that JWE have a considerably inhibitory effect on the inflammation and the skin barrier damage induced by UVB irradiation and Sq-OOH application.

• Journal of Veterinary Science
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• 제23권2호
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• pp.26.1-26.12
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• 2022

Background: Glutamate is the main excitatory neurotransmitter. Excessive glutamate causes excitatory toxicity and increases intracellular calcium, leading to neuronal death. Parvalbumin is a calcium-binding protein that regulates calcium homeostasis. Quercetin is a polyphenol found in plant and has neuroprotective effects against neurodegenerative diseases. Objectives: We investigated whether quercetin regulates apoptosis by modulating parvalbumin expression in glutamate induced neuronal damage. Methods: Glutamate was treated in hippocampal-derived cell line, and quercetin or vehicle was treated 1 h before glutamate exposure. Cells were collected for experimental procedure 24 h after glutamate treatment and intracellular calcium concentration and parvalbumin expression were examined. Parvalbumin small interfering RNA (siRNA) transfection was performed to detect the relation between parvalbumin and apoptosis. Results: Glutamate reduced cell viability and increased intracellular calcium concentration, while quercetin preserved calcium concentration and neuronal damage. Moreover, glutamate reduced parvalbumin expression and quercetin alleviated this reduction. Glutamate increased caspase-3 expression, and quercetin attenuated this increase in both parvalbumin siRNA transfected and non-transfected cells. The alleviative effect of quercetin was statistically significant in non-transfected cells. Moreover, glutamate decreased bcl-2 and increased bax expressions, while quercetin alleviated these changes. The alleviative effect of quercetin in bcl-2 family protein expression was more remarkable in non-transfected cells. Conclusions: These results demonstrate that parvalbumin contributes to the maintainace of intracellular calcium concentration and the prevention of apoptosis, and quercetin modulates parvalbumin expression in glutamate-exposed cells. Thus, these findings suggest that quercetin performs neuroprotective function against glutamate toxicity by regulating parvalbumin expression.

• Applied Microscopy
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• 제41권3호
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• pp.197-204
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• 2011

백차 열수추출물의 염증 및 피부장벽 손상완화 효과를 알아보기 위해 생후 6~7주령 암컷 SKH-1 hairless 마우스 등 부위에UVB를 12주간 조사하여 피부노화를 유발시킨 후, 실험동물을정상군(N), 대조군(UVB+saline, C), 양성대조군(UVB+0.01%retinoic acid, PC), 실험군1 (UVB+1% white tea water extract, E1), 실험군2 (UVB+2% white tea water extract, E2)로 나누어 1일 2회, 주 5일, 4주 동안 매회 200 ${\mu}L$씩 시료를 도포하여 다음과 같은 결과를 얻었다. (1) 피부 홍반도 측정에서, 실험 4주 후 C군에비해 PC, E1, E2군은 각각 31, 41, 46% 유의하게(p<0.001) 낮았다. (2) 수분함량 측정에서, 실험 4주 후 C군에 비해 PC, E1, E2군은 각각 190, 207, 225% 유의하게(p<0.001) 높았다. 경표피수분 손실량(transepidermal water loss, TEWL) 측정에서, 실험 4주후 C군에 비해 PC, E1, E2군은 각각 61, 79, 85% 유의하게(p<0.001) 낮았다. 조직학적 관찰에서, C군에 비해 E1, E2군은 표피층과 진피층의 비후, 비만세포수와 탈과립 정도가 현저하게 경감되었다. 이상의 연구결과를 종합할 때, hairless 마우스를 이용한in vivo 실험에서 백차 열수추출물 경피 도포는 자외선 조사로 인해 유발된 피부장벽 손상 및 염증 반응에 상당한 개선 효과가 있음을 확인하였다.

• 한국자원식물학회지
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• 제27권5호
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• pp.421-428
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• 2014

ICR웅성마우스에 5% DSS로 궤양성 대장염을 유발시킨 후, 정상대조군, 궤양유발군, 양성대조군 및 식방풍 잎 추출물 투여군의 궤양성 대장염에 미치는 효과를 요약한 결과는 다음과 같다. 1. 식방풍 잎 추출물 투여군은 양성대조군에 비해 체중감소 완화 효과를 나타냈지만, 농도에 따른 유의적인 차이는 나타나지 않았다. 2. 식방풍 잎 추출물 투여군의 대장조직 및 비장변화는 양성대조군과 비슷한 개선효과를 나타냈다. 3. 식방풍 잎 추출물 투여군은 혈중내 염증성 사이토카인을 농도 의존적으로 감소시켰으며, 대장조직내 염증성 사이토카인 mRNA 발현을 억제하는 효과를 나타냈다.

• 한국식품위생안전성학회지
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• 제13권2호
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• pp.87-93
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• 1998

Tannic acid(0.5mg/ml , 1.0mg/ml, 2.0mg/ml)와 카드뮴(20mg/kg)을 마우스에 경구투여한 결과는 다음과 같다. 1.Tannic acid와 카드뮴을 투여한 마우스의 증체량과 음수소비량에 변화가 있었으나, 카드뮴투여에 의한 변화는 tannic acid 투여에 의하여 감소되었다. 2. 카드뮴투여에 의하여 간장의 상대중량과 뇌 상대중량이 대조군에 비하여 유의한 변화가 있었으며, tannic acid 1.0mg/ml 투여군에서는 간장의 상대중량, 폐장의 상대중량, 흉선의 상대중량도 유의하게 변화하였다. (P<0.05). 3. Hemoglobin contents, packed cell volume, platelet count, neutrophill count 등의 혈액학적인 변화는 대조군에 비하여 카드뮴 투여군에서 유의한 변화가 인정되었다. 그러나 이러한 유의한 변화가 tannic acid를 동시 투여한 군에서는 나타나지 않았다. 4. 카드뮴을 투여한 군에서는 혈청학적 변화(ALT, AST, BUN와 creatinine)가 있었으나 tannic acid 0.5, 1.0, 2.0 mg/ml을 동시 투여한 군에서는 회복되는 경향이 나타났다. 위의 결과로 미루어 카드뮴 투여에 의한 독성이 tannic acid을 2.0mg/ml/day 이상 4주간 투여했을 때 경감효과가 나타날 수 있었다. 그러나, 카드뮴과 같은 중금속의 독성에 tannic acid가 어떻게 경감효과를 나타내는지에 대한 작용기전의 연구가 더 필요할 것으로 사료된다.

• Journal of Ginseng Research
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• 제44권3호
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• pp.442-452
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• 2020

Backgroud: Sleep deprivation (SD) impairs learning and memory by inhibiting hippocampal functioning at molecular and cellular levels. Abnormal autophagy and apoptosis are closely associated with neurodegeneration in the central nervous system. This study is aimed to explore the alleviative effect and the underlying molecular mechanism of stem-leaf saponins of Panax notoginseng (SLSP) on the abnormal neuronal autophagy and apoptosis in hippocampus of mice with impaired learning and memory induced by SD. Methods: Mouse spatial learning and memory were assessed by Morris water maze test. Neuronal morphological changes were observed by Nissl staining. Autophagosome formation was examined by transmission electron microscopy, immunofluorescent staining, acridine orange staining, and transient transfection of the tf-LC3 plasmid. Apoptotic event was analyzed by flow cytometry after PI/annexin V staining. The expression or activation of autophagy and apoptosis-related proteins were detected by Western blotting assay. Results: SLSP was shown to improve the spatial learning and memory of mice after SD for 48 h, accomanied with restrained excessive autophage and apoptosis, whereas enhanced activation of phosphoinositide 3-kinase/protein kinase B/mammalian target of rapamycin signaling pathway in hippocampal neurons. Meanwhile, it improved the aberrant autophagy and apoptosis induced by rapamycin and re-activated phosphoinositide 3-kinase/Akt/mammalian target of rapamycin signaling transduction in HT-22 cells, a hippocampal neuronal cell line. Conclusion: SLSP could alleviate cognitive impairment induced by SD, which was achieved probably through suppressing the abnormal autophagy and apoptosis of hippocampal neurons. The findings may contribute to the clinical application of SLSP in the prevention or therapy of neurological disorders associated with SD.