• Korean Journal of Acupuncture
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• 제36권1호
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• pp.63-73
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• 2019

Objectives : This study was designed to investigate the effects of Alismatis Rhizoma (AR) pharmacopuncture at BL23 on acute renal failure induced by cisplatin. Methods : The Sprague-Dawley rats were divided into Normal group (no injection of cisplatin and no treatment), Control group (cisplatin injection without treatment), Acu group (needling at BL23 after cisplatin injection), AR-PA1 group (treated with $0.3571mg/kg/20{\mu}l$ of AR pharmacopuncture at BL23 after cisplatin injection), and AR-PA2 group (treated with $1.7855mg/kg/20{\mu}l$ of AR pharmacopuncture at BL23 after cisplatin injection). Each treatment was given once daily for 8 days. Changes in body weight, kidney weight, tumor necrosis factor-alpha ($TNF-{\alpha}$), interleukin-6 (IL-6), Cu-Zn superoxide dismutase (Cu-Zn SOD), glutathione peroxidase (GPx), serum blood urea nitrogen (serum BUN), and serum creatinine were observed. Results : Body weight was significantly increased in AR-PA1 on $4^{th}$ and $6^{th}$ days and AR-PA2 on $2^{nd}$ day. $TNF-{\alpha}$ was significantly decreased in Acu, AR-PA1 and AR-PA2 groups. Cu-Zn SOD was significantly increased in AR-PA2 group. GPx was significantly increased in AR-PA1 and AR-PA2 groups. But kidney weight, IL-6, serum BUN and serum creatinine were not significantly changed in any groups compared to control group. Conclusions : In acute renal failure induced by cisplatin, AR pharmacopuncture has a mitigating effect on the inflammatory reaction related to the increase of $TNF-{\alpha}$ in the kidney tissue and a protective effect on the oxidative stress of the kidney tissue. However it is unlikely to restore the glomerular function or inhibit the renal swelling.

• Preventive Nutrition and Food Science
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• 제19권3호
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• pp.129-135
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• 2014

The protective role of phloroglucinol against oxidative stress and stress-induced premature senescence (SIPS) was investigated in vitro and in cell culture. Phloroglucinol had strong and concentration-dependent radical scavenging effects against nitric oxide (NO), superoxide anions ($O_2{^-}$), and hydroxyl radicals. In this study, free radical generators were used to induce oxidative stress in LLC-PK1 renal epithelial cells. Treatment with phloroglucinol attenuated the oxidative stress induced by peroxyl radicals, NO, $O_2{^-}$, and peroxynitrite. Phloroglucinol also increased cell viability and decreased lipid peroxidation in a concentration-dependent manner. WI-38 human diploid fibroblast cells were used to investigate the protective effect of phloroglucinol against hydrogen peroxide ($H_2O_2$)-induced SIPS. Phloroglucinol treatment attenuated $H_2O_2$-induced SIPS by increasing cell viability and inhibited lipid peroxidation, suggesting that treatment with phloroglucinol should delay the aging process. The present study supports the promising role of phloroglucinol as an antioxidative agent against free radical-induced oxidative stress and SIPS.

• 한국식품위생안전성학회지
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• 제26권2호
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• pp.107-113
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• 2011

현대사회는 생활습관, 공해, 오염, 독성물질 등 여러 종류의 산화스트레스를 받는 환경에 노출되어 있으며, 이런 산화스트레스들은 인간에게 있어 여러 질병을 야기한다는 많은 증거 들이 나오고 있다. Ferric Nitrilotriacetate (Fe-NTA)는 iron-induced oxidative Stress로 인해 신장독성에 관여되어 있다고 보고된 물질이다. 이에 본 연구진은 랫드에 항산화 효과가 있는 차전초(Plantago asiatica) 추출물을 투여하고 Fe-NTA를 복강 주사하여 선장에서 iron-induced oxidative stress를 유발한 후, 산화스트레스를 얼마나 억제하여 주는 지를 혈액에서 신장기능 지표인 blood urea nitrogen (BUN)과 creatinine (Cr)을 측정하고, 신장조직에서는 항산화 바이오마커들인 reduced glutathione (GSH), glutathione-S-transferase (GST), glutathione reductase (GR) 및 지질과산화물 (lipid peroxide)인 malondialdehyde (MDA)를 측정 하였다. 신장기능 이상시 증가되는 BUN 및 Cr은 Fe-NTA에 의해 산화스트레스만 유발한 그룹에서는 $116.82{\pm}5.20$ mg/dL과 $2.70{\pm}0.20$ mg/dL로 아무것도 처리하지 않은 대조군의 $18.54{\pm}1.29$ mg/dL, $0.52{\pm}0.04$ mg/dL에 비해 약 6.3배 및 5.2배의 증가를 나타냈다. 반면 차전초를 투여한 1g/kg b.w. 군에 서 BUN 및 Cr의 활성 이 각각 $95.76{\pm}7.89$ mg/dL과 $2.16{\pm}0.340$ mg/dL, 2g/kg b.w. 군에서는 $89.34{\pm}26.93$ mg/dL 과 $2.20{\pm}0.51$ mg/dL, 4 g/kg b.w. 군에서는 $39.54{\pm}21.93$ mg/dL과 $1.16{\pm}0.55$ mg/dL으로 농도 의존적으로 유의적 (p < 0.05) 차이를 보이며 감소하는 결과를 보였다. 항산화의 바이오마커로 작용하는 GSH, GST 및 GR은 Fe-NTA에 의해 산화스트레스만 유발한 그룹에서는 각각 $59.45{\pm}12.32$ mmol GSH/g tissue, $49.88{\pm}4.55$ Units/g tissue, $56.70{\pm}5.40$ Units/g tissue로 아무것도 처리하지 않은 정상그룹의 $142.82{\pm}16.51$ mmol GSH/g tissue, $124.69{\pm}13.073$ Units/g tissue, $107.31{\pm}8.70$ Units/g tissue에 비해 58.4%, 60.0%, 47.2%로 현저하게 감소하였다. 반면 차전초 추출물을 1, 2, 4 g/kg b.w. 으로 투여한 그룹에서의 GSH는 $77.86{\pm}12.62$, $123.11{\pm}12.72$, $147.97{\pm}26.27$ mmol GSH/g tissue로 Fe-NTA만 처리한 그룹에 비해 약 1.3배, 2.1배, 2.5배 증가하였으며, GST는 $66.59{\pm}5.01$, $83.25{\pm}8.38$, $124.68{\pm}13.67$ Units/g tissue.로1.3배,1.7배, 2.5배 증가, GR은 $67.37{\pm}8.66$, $80.34{\pm}6.06$, $98.67{\pm}10.11$ Units/g tissue로 1.2배, 1.4배, 1.7배 증가하였다. 산화스트레스로 유발되는 지질과산화물을 신장에서 측정 하였을 때 Fe-NTA에 의해 산화스트레스만 유발한 그룹은 $215.70{\pm}49.73\;{\mu}mol$/g tissue로 대조군 그룹의 $46.20{\pm}10.65\;{\mu}mol$/g tissue보다 지질과산화를 많이 일으켜 4.7배 많은 MDA를 생성한 것을 나타냈지만, 차전초 추출물 1, 2,4 g/kg b.w. 투여한 그룹은 MDA의 생성량이 $141.74{\pm}10.79$, $116.11{\pm}9.19$, $86.52{\pm}22.30\;{\mu}mol$/g tissue로 약 34.3%, 46.2%, 59.9% 감소한 것을 확인하였다. 신장에서 iron-induced oxidative stress에 의해 독성을 유발하는 Fe-NTA를 처리 하였을시 신장손상 지표인 BUN과 Cr은 증가하고, 항산화 지표인 GSH와 GST, GR은 감소함과 동시에 지질과산 화물인 MDA는 증가하였다. 그러나 차전초 추출물을 농도를 달리하여 투여한 후 Fe-NTA로 산화스트레스를 유발한 그룹은 농도 의존적으로 BUN과 Cr은 감소하고, 항산화 지표들은 증가함과 동시에 MDA는 감소하는 경향을 보였으며 Fe-NTA만 처리한 그룹과 유의적 차이를 보였다. 위 결과들을 종합하면 Fe-NTA는 산화스트레스에 의해 신장에 심각한 손상을 줄 수 있으며, 차전초 추출물은 항산화 효과를 바탕으로 하여 Fe-NTA에 의한 신장 손상에 대한 보호 또는 개선 효과가 있음을 확인 하였다.

• Korean Journal of Acupuncture
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• 제23권1호
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• pp.45-57
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• 2006

Objective : This study was undertaker to determine if Juglandis Semen herbal acupuncture (JSA) exerts protective effect against alterations in membrane transport function in rabbits with mercury-induced acute renal failure. Methods : Nephrotoxicity was induced by subcutaneous administration of Hg(a single dose of 10mg/kg) and JSA was performed at both sides of Shenshu($(BL_{23})$, Sinsu) for 7 days. Results: The administration of Hg at a subcutaneous single dose of 10 mg/kg caused a reduction in GFR to 12% of the basal value and an increase in fractional $Na^+$ excretion to 8.9-fold, indicating generation of acute renal failure. When JSA were given for 7 days prior to Hg administration, such changes were significantly attenuated. The fractional excretion of glucose and phosphate was increased to approximately 102- and 35-fold, respectively, in rabbits treated with Hg alone. The increase in rabbits treated with Hg following ISA are significantly lower than that in animals treated with Hg alone. Uptakes of glucose and phosphate in purified isolated brush-border membrane and $Na^+-K^+-ATPase$ activity in microsomal fraction were inhibited in rabbits treated with Hg alone, suggesting that impairment in proximal reabsorption of glucose and phosphate is resulted from a direct damage of membrane transport carriers and disruption of the normal $Na^+$ gradient. Such changes were prevented by JSA. Conclusion These results indicate that the administration of Hg causes impairment in reabsorption of solutes in the proximal tubule via the generation of reactive oxygen species. JSA provides the protection against the Hg-induced impairment in proximal reabsorption, and its effect may be resulted from its antioxidant action.

• 동의생리병리학회지
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• 제17권2호
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• pp.316-325
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• 2003

In this paper, the effect of Ganopoly(extracts of Ganoderma lucidum) and Ganopoly/C+(70% Ganopoly + 30% chitosan) on cisplastin-induced nephrotoxicity was investigated in Sprague-Dawley rats. A single dose of cisplastin(5 ㎎/㎏) kg) was administered intraperitoneally after pretreatment of saline, Ganopoly and Ganopoly/C+ for 7 days. The nephrotoxicity and renal function were manifestated by the changes of body weight, blood pressure, biochemical changes and solute in urine and plasma. After the treatment of CDDP(cis-dichlorodiamineplatinum), a significant elevation of kidney weight, serum urea, cretinine, urine volume for 24 hours, urine magnesium, and a severe or significant decrease in body weight, blood pressure, creatinine clearance, urine osmolarity, serum albumin, etc. The nephrotoxicity was further confirmed by a significant decrease in glutathione S-transferase(GSH) in urine and kidney homogenate, GSH, glutathione peroxidase(GSH-Px) and catalase in kidney tissue. And also the lipid peroxidation was significantly increased in kidney homogenate. These signs of nephrotoxicity was ameliorated by the pretreatment and consecutive administration of Ganopoly and Ganopoly/C+ for 14 days after the Lp. injection of CDDP on 7th day after pretreatment of Ganopoly and Ganopoly/C+. The amelioration of nephrotoxicity was evidenced by significant reduction in serum urea and creatinine concentration, and improvement of other index of renal function. And The activity of antioxidant enzymes were partially recovered in kidney tissue of rats treated by CDDP and the administration of Ganopoly and Ganopoly/C+. These results indicate the cispastin induced nephrotoxicity is due to an impairment of tubular reabsorption systems enhanced by necrosis of proximal tubule, and the Ganopoly and Ganopoly/C+ has a partial protective effect on nephrotoxicity induced by CDDP. The polysacchride of Ganoderma lucidum may improve the therapeutic index of nephrotoxicity induced by CDDP. However, it is needed to elucidate the mechanism for confirming the therapeutic effect.

• 대한한의학방제학회지
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• 제28권3호
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• pp.271-280
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• 2020

Hypertension has been approved to cause disharmony between the heart and kidney such as cardiac hypertrophy and kidney dysfunction. In traditional oriental medicine Paeo-tang (PET) has been shown to have effects on blood circulation improvement. However, the beneficial effect of PET on hypertension remains unknown. In this study, we investigated that PET attenuates blood pressure and improves cardiovascular and renal function in NG-nitro-L-arginine methylester (L-NAME) rat model. Hypertensive rat models were induced by the administration of L-NAME (40 mg/kg/day) and then PET (50 or 100 mg/kg/day) or Olmetec was treated for 2 weeks. PET treatment significantly suppressed the systolic blood pressure and decreased intima-media thickness in the thoracic aorta. PET ameliorated endothelium-dependent and independent vascular relaxation in the L-NAME-induced vascular dysfunction. PET ameliorated the functional decline in the kidney such as albumin and blood urea nitrogen in plasma. These results demonstrated that PET possesses protective effects against L-NAME-induced hypertension.

• 대한한의학회지
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• 제27권1호
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• pp.47-56
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• 2006

The present study was carried out to investigate the preventive effect of Epimedii Herba combined Samgijiwhang-Tang(SJTE) on streptozotocin(STZ)-induced diabetic nephropathy. SJTE was given to rats with oral administration. The experimental animals were divided into normal group of rats, control group of STZ-induced diabetic rats, and sample group with SJTE administration. Experimental diabetic nephropathy was induced by the injection of STZ(60mg/kg) to the rat via the peritoneum. The effect of SJTE on STZ-induced diabetic nephropathy was observed by measuring the serum level of insulin, glucose, creatinine and BUN. Urine secretion of albumin for 24 hours and urine level of glucose measures too. Anti-oxidative stress of STZ administration in living body was estimated by measuring lipid peroxide in cortex of kidneys. STZ induced increase of serum glucose. creatinine, urine albumin secretion and renal cortical lipid peroxidation were lowered by SJTE administration. In conclusion, the SJTE treatment showed protective effect on rat diabolic nephropathy model, and action mechanism of the effect was thought to be concerned with internal glucose metabolism.

• 대한본초학회지
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• 제21권3호
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• pp.75-81
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• 2006

Objectives : The present study was carried out to investigate the beneficial effect of Coicis Semen extract(CSe) on streptozotocin(STZ)-induced diabetic nephropathy rats. CSe was given to rats with oral administration. Methods : The experimental animals were divided into 3 groups : normal group of rats, control group of STZ-induced diabetic rats, sample group with CSe treatment. Experimental diabetes was induced by the injection of STZ(60 mg/kg) to the rat via the peritoneum. The effects of CSe on STZ-induced diabetic nephropathy were observed by measuring the serum level of creatinine, BUN and uric level of glucose. Kidney level of lipid peroxidation and the activities of reduced glutathione(GSH) were also examined Results : STZ-induced increase of serum creatinine was lowered by CSe treatment, but BUN and uric level of glucose did not show significant changes. CSe oral administration showed statistical decrease of lipid peroxidation in renal cortical tissues, but it has no effect on the activities of GSH. Conclusion : CSe treatment showed protective effect on rat diabetic nephropathy model, but action mechanism of the effect was still not dear. We thought to be concerned with anti-oxidative stress.

• 한국약용작물학회지
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• 제25권4호
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• pp.231-237
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• 2017

Background: Cisplatin is one of the most extensively used chemotherapeutic agents for the treatment of cancer, including bladder, and ovarian cancers. However, it has been shown to induce nephrotoxicity, despite being an outstanding anti-cancer drug. In this study, we investigated the protective effect of dopaol ${\beta}$-D-glucoside (dopaol) on cisplatin-induced nephrotoxicity. Methods and Results: To confirm the protective effect of dopaol on cisplatin-induced nephrotoxicity, HK-2 cells were treated with $20{\mu}M$ cisplatin and $80{\mu}M$ dopaol. Cisplatin increased apoptosis, caspase-3 activity and mitochondrial dysfunction; however pretreatment with $80{\mu}M$ dopaol successfully attenuated apoptosis, caspase-3 activity and mitochondrial dysfunction. To evaluate the protective effect dopaol on cisplatin-induced nephrotoxicity in vivo, we used an animal model (balb/c mice, 20 mg/kg, i.p. once/day for 3 day). The results were similar to those obtained using HK-2 cells; renal tubular damage and neutrophilia induced by cisplatin reduced following dopaol injection (10 mg/kg, i.p. once/day for 3 day). Conclusions: These results indicate that dopaol treatment reduced cisplatin-induced nephrotoxicity in vitro and in vivo, and can be used to treat cisplatin-induced nephrotoxicity. However, further studies are required to determine the toxicity high dose dopaol and the signal pathways involved in its mechanism of action in animal models.

• 한국식품과학회지
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• 제46권5호
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• pp.641-647
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• 2014

당뇨 모델 쥐에서 매생이 추출물과 그 지표물질인 pheophorbide A의 신장 보호 효과를 확인하였다. 5주령의 SD 랫드를 일주일간 순화시킨 뒤 40 mg/kg BW의 농도로 streptozotocin을 복강 투여하였으며, 한달 동안의 유도기간을 거쳐 모든 당뇨 유발군에서 혈당이 400-500 mg/dL가 된 것을 확인한 이후 9주 동안의 샘플 투여를 진행하였다. 신장 손상과 관련한 혈액 생화학적 지표인 BUN, creatinine에서는 당뇨 유발군 사이에 개선되는 경향을 보이진 않았다. 신장 조직에서 산화스트레스에 의해 유발되는 지질 과산화물을 측정 하였을 때 당뇨 유발군인 STZ군($0.19{\pm}0.04$)은 정상 대조군인 Con군($0.05{\pm}0.00$)에 비하여 3.5배 많은 MDA를 생성하였지만 매생이 추출물 4, 20 mg/kg BW투여한 CL, CH군은 MDA의 생성량이 $0.05{\pm}0.02$, $0.08{\pm}0.02$, 지표물질인 pheophorbide A를 0.2 mg/kg BW을 투여한 PhA군은 0.12{\pm}0.01 nmol/mg protein로 샘플 투여군에서 과산화물이 유의적으로 감소하는 것으로 보아(p<0.05) CFE와 PhA의 항산화 작용을 확인할 수 있었다. 항산화 바이오 마커인 GSH와 GSSH 함량 및 GPx, GR, GST 활성을 측정한 결과 CFE와 PhA는 산화스트레스에 의한 신장 조직의 GSH 함량이 감소하는 것을 막아 당뇨로 인한 신장 손상에 보호 효과가 있는 것을 확인하였다(p<0.05). 또한 STZ에 유도된 당뇨 쥐의 신장 조직엔 많은 양의 과산화물이 축적되어 있으며 이를 소거하기 위해 GPx의 활성이 높아졌는데, AC군과 PhA군에서 GPx 의 증가 정도를 유의적으로 완화시켰다(p<0.05). GR 활성은 CL, CH, PhA군에서 Con군 수준까지 올라오는 것으로 보아 신장의 산화적 손상을 정상수준까지 회복 시키는 것으로 보였으며, GST 결과로 미루어 보아 CFE와 PhA는 신장 조직에서 일차적으로 과산화물을 포집하고 GSH를 이용하여 체내의 독성 물질을 분해시켜 STZ로 유도된 당뇨로부터 신장 보호 효과를 나타내었다. 또한, 조직 내에서 SOD와 CAT의 활성 측정 결과, CFE와 PhA는 지질과산화물의 증가로 산화적 손상이 가속화 될 때, 항산화 효소계의 활성을 증가시키고 산화 스트레스에 의한 조직 손상을 완화 시켜 주는 것으로 확인되었다. 신장 조직의 병리학적 관찰 결과 CL, CH 및 PhA군에선 STZ군에 비해 비이상적인 글리코겐의 축적이 유의적으로 저해 되는 것을 관찰할 수 있었다(p<0.05). 위와 같은 실험 결과를 통하여 매생이 추출물과 PhA가 당뇨병성 신장 손상에 보호 효과가 있다는 것을 확인하였다.