• Journal of Plant Biotechnology
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• 제41권2호
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• pp.73-80
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• 2014

산화질소(nitric oxide: NO) 공여체인 $100{\mu}M$ sodium nitroprusside (SNP)를 배추 잎에 전처리한 후 이어서 $2{\mu}M$ paraquat (PQ)처리 시, PQ에 의해 유도된 산화적 손상에 대한 잎의 내성이 효과적으로 증진되었다. 24 시간 광 배양기간 동안 PQ 단독 처리구 잎에서는 생체량, 엽록소 및 단백질 함량이 현저하게 감소하였으나 PQ 노출 전에 3시간 SNP 전처리로 이들 잎 손상이 의미 있게 완화되었다. 게다가 PQ 처리에 기인된 malondialdehyde (MDA)와 $H_2O_2$ 함량 증가도 SNP 전처리에 의해 유의하게 억제되었다. 잎에서 이들 PQ 독성에 대한 SNP의 방어효과와 관련하여 ascorbate-glutathione 회로 구성 효소의 활성도 변화를 조사하였다. PQ 단독 처리구에서 APX, DHAR 및 GR 효소 활성도는 배양 6시간후에 급격히 감소되어 대조구 잎과 비교 시 각각 대조구의 19%, 50%, 39% 수준의 활성도 값을 보였다. 그러나, 이들 효소 활성도 값 감소는 SNP 전처리에 의해 현저하게 억제되어 6시간 배양 후에 PQ 단독처리구 보다 각각 5배, 2배, 1.5배 높은 값을 나타내었다. 또한, 그 이후 24시간 배양 때까지 PQ 단독 처리구보다 계속 높은 활성도를 보이면서 점차로 감소하였다. 이들 결과로부터, PQ에 노출된 배추 잎에서 SNP 전처리에 의한 ascorbate-glutathione 회로의 활성화가 $H_2O_2$의 축적을 억제하며 그로인해 PQ에 의해 유도된 산화스트레스로부터 잎을 방어하는 것으로 생각되었다. 동시에 이 들 결과는 산화질소가 배추 잎에서 PQ 스트레스에 대한 항산화 방어자로서의 역할을 하는 것을 의미한다.

• Toxicological Research
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• 제13권4호
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• pp.393-400
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• 1997

The effects of superoxide dismutase(SOD) and catalase on the toxicity of paraquat(PQ) were studied using diethyldithiocarbamate(DDC), 3-amino-1,2,4-triazole(AT) which are inhibitors of Cu, Zn-SOD and catalase in rats. Sprague Dawley rats were divide into 6 groups: control, DDC, PQ, AT, DDC+PQ, and AT+PQ group. The PQ (50 mg/kg body weight(BW); about half dose of $LD_{50}$) was administered with orally, otherwise AT(1.0g/kg BW) and DDC(1.0g/kg BW) were administered by intrperitoneal(iP) injection. The survival rate of rats in PQ+AT group was significantly decreased compared with PQ group while the difference of survival rate between DDC group and DDC+PQ group was not significant. The SOD activity after administration of DDC was decreased in liver, lung and kidney, but catalase activity was not changed. The catalase activity in liver, lung and kidney of AT treated rats was decreased, while SOD activity was not changed in this group. The effects of DDC and AT to the PQ toxicity was also observed in primary cultured rat Skin fibroblasts. The viable cells that was measured with MTT method, was decreased in AT+PQ treated group compared to PQ treated group, but the difference of cell viability between DDC treat group and DDC+PQ treated group was not observed. This result, AT potentlate PQ toxicity while DDC were not affect, suggested that the decreased catalase activity lead to elevation of hydrogen peroxide levels and PQ toxicity may be correlate with the hydrogen peroxide rather than the superoxides.

• 약학회지
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• 제43권6호
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• pp.809-817
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• 1999

The effect of 2-(4-cyanophenyl)amino-1,4-naphthalenedione-3-pyridinium perchlorate (PQ5) on pla-telet aggregation and its action mechanisms were investigated with rat platelet. PQ5 inhibited the platelet aggregation induced by collagen ($6{\;}{\mu\textrm{g}}/ml$), thrombin (0.4 U/ml) and A23187 ($3{\mu}M$) in concentration-dependent manner with $IC_{50}$ values of 5.50, 25.89 and $37.12{\;}{\mu}M$, respectively. PQ5 also significantly reduced the thromboxane $A_2$ (TXA2) formation in a concentration dependent manner. The collagen-induced arachidonic acid (AA) release in [-3H]-AA incorporated platelet, an indication of the phospholipase $A_2$ activity, was decreased by PQ5 pretreatment PQ5 significantly inhibited the activity of thormboxane synthase only at high concentration ($100{\mu}M$), but did not affect the cyclooxygenase activity at all. Collagen-induced ATP release was significantly reduced by PQ5. Calcium-induced platelet aggregation experiment suggests that the elevation of intracellular free $Ca^{2+}$ concentration ($[Ca^{2+}]_i$) by collagen stimulation is decreased by the pretreatment of PQ5, which is due to the inhibition of calcium release from intracellular store and influx from outside of the cell. PQ5 did not showed the effect of anticoagulation as prothrombin time (PT) or activated partial thromboplastin time (APTT). Form these results, it is suggested that PQ5 exerts its antiplatelet activity through the inhibition of the intracellular $Ca^{2+}$ mobilization and the decrease of the $TXA_2$ synthesis.

• 대한의생명과학회지
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• 제8권2호
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• pp.71-75
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• 2002

Paraquat (N,N'-dimethyl-4,4'-bipyrrimidinium-dichlorides (PQ): MW 186.6) has been used to killing verierty of hubside plants. For this study were use Sprague-dawely rats (190$\pm$10 gm) and injection 40 mg/kg BW of paraquat (LD$_{50}$) to 24 hrs PQ and 4 days PQ group excepte normal control. For the measurement of blood calcium Ino-phosphorus and activity of alkaline phosphatase (ALP) by HITTACH 746. In serum phosphoruse of normal control were 8.0$\pm$1.2 mg/dl and 24 hrs PQ group were 8.9$\pm$1.0 mg/dl (P<0.05) and 4 days PQ group were 8.8$\pm$0.42 gmm/dl (P<0.05). In serum phosphorus were very sensitive uptaked to 10% within only 24 hours, but 4 days of PQ were similar uptake level than 24 hrs PQ. So this 8.9 mg/dl of sem phosphorus may be thought threshold level becouse does not more encrease. In blood calcium normal of rats were measured 9.51$\pm$0.3 mg/dl and 24 hrs of PQ group were 9.9$\pm$0.51 mg/dl (uptaked 4.5%, p>0.05). This uptake cannot fined meaning mathmatic statistics but 4 days PQ groups of calcium were 10.43$\pm$0.37 gm/dl (uptaked 10%, p<0.05). That 24 hrs PQ groups of caclium dose not reacted sensitive to irritated by PQ. So, when use oxidants of PQ, the blood calcium and Ino-phosphorus were linear correlated uptake that reasone thought may be move out form hardness bone tissue to in blood it does not take feeding to hunger for 4 days. In ALP normal of rats were measured 991$\pm$106 unit/L. In 24 hrs irritated PQ rats were fall down by 629$\pm$91 unit/L (P<0.001) but in 4 days of PQ rats were 792$\pm$85 unit/L (P<0.0011) that the activity of level were mild recovered activity from 629 unit (63%) to 792 unit (80%). So, that the reasone of ALP were very sensitive activity and reverse correlated to blood calcium or phosphorus irritated by PQ.

• 한국환경과학회지
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• 제1권2호
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• pp.81.1-86
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• 1992

The amounts of ascorbic acid in chloroplasts treated with light and light+paraquat (PQ) were reduced by 81 and 82% of initial level, respectively at 24 hr at incubation. And those treated with dark and dark+PQ were decreased by W and 55% of the original level, respectively. Malondialdehyde (MDA) contents at 24 hr of dark and dark+PQ treatment were increased by 6 and 31% of the initial level, respectively. When chloroplasts were treated with light and light+PQ, MDA contents after 24 hr were increased by 88 and 146% of the initial level, respectively. SOD activities treated with light and light+PQ were increased by 10 and 20% of the initial level, respectively for 3 hr and thereafter reduced by 46 and 49% of the original level, respectively at 24 hr. However, the SOD activities treated with dark and dark+PQ were decreased by 37 and 30% of the initial level, respectively. It is considered that PQ triggers the oxidation of ascorbic acid, the induction of lipid peroxidation and the inactivation of SOD under light so that PQ has inhibitors effect on the pathway of plant metabolism. Key word: ascorbic acid, malondialdehyde, superoxide dismutase, paraquat, lipid peroxidation.

• Environmental Sciences Bulletin of The Korean Environmental Sciences Society
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• 제1권2호
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• pp.81-86
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• 1997

The amounts of ascorbic acid in chloroplasts treated with light and light+paraquat (PQ) were reduced by 81 and $82\%$ of initial level, respectively at 24 hr at incubation. And those treated with dark and dark+PQ were decreased by 46 and $55\%$ of the original level, respectively. Malondialdehyde (MDA) contents at 24 hr of dark and dark+PQ treatment were increased by 6 and $31\%$ of the initial level, respectively. When chloroplasts were treated with light and light+PQ, MDA contents after 24 hr were increased by 88 and $146\%$ of the initial level, respectively. SOD activities treated with light and light+PQ were increased by 10 and $20\%$ of the initial level, respectively for 3 hr and thereafter reduced by 46 and $49\%$ of the original level, respectively at 24 hr. However, the SOD activities treated with dark and dark+PQ were decreased by 37 and $30\%$ of the initial level, respectively, It is considered that PQ triggers the oxidation of ascorbic acid, the induction of lipid peroxidation and the inactivation of SOD under light so that PQ has inhibitory effect on the pathway of plant metabolism.

• Journal of Ginseng Research
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• 제44권5호
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• pp.680-689
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• 2020

Background: Peptides have diverse and important physiological roles in plants and are ideal markers for species identification. It is unclear whether there are specific peptides in Panax quinquefolius L. (PQ). The aims of this study were to identify Quinetides, a series of diverse posttranslational modified native peptides of the ribonuclease-like storage protein (ginseng major protein), from PQ to explore novel peptide markers and develop a new method to distinguish PQ from Panax ginseng. Methods: We used different fragmentation modes in the LTQ Orbitrap analysis to identify the enriched Quinetide targets of PQ, and we discovered Quinetide markers of PQ and P. ginseng using ultrahigh-performance liquid chromatography-quadrupole time-of-flight mass spectrometry analysis. These "peptide markers" were validated by simultaneously monitoring Rf and F11 as standard ginsenosides. Results: We discovered 100 Quinetides of PQ with various post-translational modifications (PTMs), including a series of glycopeptides, all of which originated from the protein ginseng major protein. We effectively distinguished PQ from P. ginseng using new "peptide markers." Four unique peptides (Quinetides TP6 and TP7 as markers of PQ and Quinetides TP8 and TP9 as markers of P. ginseng) and their associated glycosylation products were discovered in PQ and P. ginseng. Conclusion: We provide specific information on PQ peptides and propose the clinical application of peptide markers to distinguish PQ from P. ginseng.

• 한국응용약물학회:학술대회논문집
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• 한국응용약물학회 2003년도 Annual Meeting of KSAP : International Symposium on Pharmaceutical and Biomedical Sciences on Obesity
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• pp.108-108
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• 2003

The current study was performed to observe the effects of Panax ginseng (PG) and P. quinquefolia (PQ) on hemodynamics such as blood flow rate (BF), blood flow velocity (BV), heart rate (HR), systolic blood pressure (SBP) and diastolic blood pressure (DBP, and body temperature (BT) in healthy young men. After testing equality of variance, Student's t-test using PROC TTEST was examined to. prove statistical differences between control and ginseng conditions at each time point. It was found that the BF data were fluctuated by personal deviation. In order to minimize the deviation, the results obtained for 6 hrs were reconstituted after dividing them into two periods of the first half from 1 to 3 hrs and of the latter half from 3.5 to 6 hrs. And then the reconstitution data and dose-response curves were obtained. Blood flow such as BF and BV shows significant increases both two periods in the dose of PG 2.25 and PG 9.0, whereas significant decrease in the dose of PG 4.5. However, in the PQ groups, the middle dose PQ 4.5 shows the highest significant increase among the three doses. Except for PG 2.25 in HR, other doses show significant decreases both in the first half and latter half. SBP of PQ 9.0 shows only a significant decrease in the first half; on the other hand, in the latter half, PG 4.5, PG 9.0 and PQ 9.0 significantly increase SBP. In addition, DBP of PG 2.25 and PG 4.5 show significant increase in the both periods. In the BT, PQ groups show gradual decrease from PQ 2.25 to PQ 9.0; however, PG groups show differently. PG 4.5 shows significant decrease, but PG 9.0 shows a increase without statistical meanings. In summary, PG is more effective in respect to keeping homeostasis of hemodynamics.

• 농촌의학ㆍ지역보건
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• 제36권4호
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• pp.218-226
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• 2011

널리 사용되고 있는 제초제인 파라콰트가 수중이나 토양을 통해 인체에 노출될 가능성이 있음을 알아보기 위해 본 연구를 시행하였다. 수중에서 자외선에 의한 파라콰트의 분해 여부를 측정하였고, 토양에 파라콰트 살포 후 인공강우조건을 만들어 파라콰트의 침출 여부를 파악하였다. 또한, 용존산소량에 따라 등급이 다른 세가지 하천수에서 파라콰트의 자외선에 의한 분해양상을 조사하였다. HPLC/UVD를 이용한 토양과 수중에서 파라콰트의 용출 및 분해양상을 살펴본 결과 수중에서 자외선에 의한 파라콰트의 분해는 일어나지 않았고, 토양에서 파라콰트 살포 후, 파라콰트 용출 여부를 한 달간 살펴보았는데 용출은 되지 않았다. 그리고 하천수의 수질에 따른 파라콰트의 자외선에 의한 영향 또한 변화가 없었다. 분석방법에 대한 검출한계는 1.57 ${\mu}g$/L로 검출한계가 낮았다. 그리고 분석의 정밀도 및 정확도를 본 결과 3개의 다른 농도에서 6 % 이내의 정밀도와 약 88 % 이상의 정확도를 갖고 있어서 분석방법이 우수하였다. 토양에 살포된 파라콰트가 강수 등에 의해서 다시 용출될 가능성은 매우 낮다. 그러나 어떠한 경로이던 수계로 들어간 파라콰트는 오랫동안 잔류되어 인체에 노출될 수 있다는 것을 알 수 있었다. 본 연구는 실험실에서 진행된 것으로 실제 환경매체를 이용한 실증적인 연구와 이를 통한 역학적 연구가 필요하다고 할 수 있다.

• 생명과학회지
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• 제18권1호
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• pp.129-135
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• 2008

Paraquat (PQ)는 전세계적으로 사용되고 있는 제초제의 한 종류이며 독성을 가지고 있다. 가자(terminalia Chebulae)는 오래전부터 설사, 이질, 디프테리아, 기침, 천식 등의 치료제로 중국, 한국 등에서 사용되고 있는 약용식물이다. TCM이 PQ 유도독성에 미치는 영향을 실험한 결과 다음과 같은 결과들을 얻었다. 1. 신장 조직과 폐 조직에서 지질과산화물 함량을 측정해본 결과 PQ 처리군은 정상군에 비해 각각 2배, 2.5배 증가하였으나 TCM 투여군에서는 정상군에 가깝게 감소하였다. 2. 활성산소 생성계 효소에서 cytosolic enzyme system인 aldehyde oxidase, xanthine oxidase 그리고 microsomal enzyme system인 aminopyrine N-demethylase, aniline hydroxylase 활성을 측정한 결과 PQ 처리군에서 활성증가가 나타났으나 TCM 투여군에서는 효소활성이 소량 감소하였다. 3. 활성산소 해독계에 영향을 미치는 superoxide dismutase, catalase, glutathione peroxidase를 측정 한 결과 PQ 처리군은 정상군에 비해 2배 이상의 활성 증가가 나타났고 TCM 투여군의 경우 소량 감소하는 결과가 얻어졌다. 4. 폐 조직의 G-6-phosphatase는 PQ투여군의 경우 활성 저하가 나타났으나 TCM 투여군에서는 효소 활성이 점차 증가하여 300 mg/ml에서는 정상군에 가까운 수치가 나타났다. 5. 폐 조직 중의 collagen 함량은 PQ 투여군의 경우 정상군에 비해 1.5배 증가하였고 가자 메탄올추출물 투여군의 경우 100 mg/kg, 200 mg/kg, 300 mg/kg의 순서로 함량이 점차 감소하는 결과를 얻을 수 있었다. 이상의 결과를 종합하여 볼 때 가자 메탄올추출물은 PQ 유도독성을 신장 및 폐조직에서 효과적으로 경감시키는 것으로 나타났다.