• The Korean Journal of Physiology and Pharmacology
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• 제1권1호
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• pp.71-78
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• 1997

In an attempt to investigate the role of phospholipase $A_2$($PLA_2$) in interleukin-l (IL-l) induced acute lung injury, mepacrine was tried to inhibit $PLA_2$ in IL-l induced ARDS rats. For confirmation of acute lung injury by IL-l, and to know the role of neutrophils in this injury, lung leak index, lung myeloperoxidase(MPO), number of neutrophils and protein content in the bronchoalveolar lavage (BAL) and wet lung weight were measured. At the same time lung $PLA_2$ was measured to know the effect of IL-l on $PLA_2$ activity. Pulmonary surfactant was also measured for an investigation of type II alveolar cell function. Neutrophil adhesion assay was performed to know the effect of $PLA_2$ inhibition in vitro with human umbilical vein endothelial cells (HUVEC). For precise location of injury by IL-l, morpholgical study was performed by electron microscopy. Five hours after instillation of IL-l (50 ng/rat), lung leak index, protein content, number of neutrophils, lung MPO and wet lung weight were increased significantly. Five hours after IL-l instillation lung $PLA_2$ activity was increased significantly, and increased surfactant release was observed in IL-l induced ARDS rats' BAL. In contrast, in rats given mepacrine and IL-l, there was decrease of acute lung injury i.e. decrease of lung leak index, wet lung weight, protein content, number of neutrophils in BAL and decreased lung MPO activity. Mepacrine decreased surfactant release also. Interestingly, inhibition of $PLA_2$ decreased adhesion of human neutrophils to HUVEC in vitro. Morphologically, IL-l caused diffuse necrosis of endothelial cells, type I and II epithelial cells and increased the infiltration of neutrophils in the interstitium of the lung but after mepacrine treatment these pathological findings were lessened. On the basis of these experimental results it is suggested that $PLA_2$ has a major role in the pathogenesis of acute lung injury mediated by neutrophil dependent manner in IL-l induced acute lung injury.

• Asian-Australasian Journal of Animal Sciences
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• 제16권6호
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• pp.889-893
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• 2003

Immunomodulatory and therapeutic potential of Enrofloxacin was studied in bovine sub clinical mastitis (SCM). The therapeutic efficacy was adjudged by Somatic cell count and Total bacterial count of the milk, whereas, the immuno modulatory potential of the drug was assessed by measuring myeloperoxidase (MPO) and acid phosphates (ACP) enzyme level in the milk leukocytes. Forty-five cows were divided into three equal groups. Gr I consisting 15 cows served as healthy control, whereas, 30 cows (SCM), Gr II and Gr III, selected on the basis of California Mastitis Test (CMT) positive reaction. Gr II cows received 150 mg of Enrofloxacin, once a day for three days and Gr.III received sterile 5 ml PBS (pH 7.4) for 7days, both the treatment were given by intramammary route. The observation was made up to 30 days post-treatment (PT). The CMT of the healthy milk was negative (0), whereas, it ranged between 1 point score and 2 point score in SCM. The Somatic cell count (SCC) and Total bacterial count (TBC) decreased significantly (p<0.05) on day 3 PT in GrII cows in Enrofloxacin treated group, however, such changes were insignificant in PBS treated group. Traces of MPO and ACP enzyme were found in the healthy milk. The mean ACP level enhanced by 70% on day 3 PT in GrII and only 18.7% in Gr. III cows. The mean MPO level enhanced to 32% in Gr. II and 18 % in Gr. III cows on day 3 PT. Concomitant use of Enrofloxacin in SCM at sub optimal dose was found to reduce the bacterial load by increasing the bactericidal enzyme level in the milk polymorphonuclear cells (PMNs) in bovine SCM, which indicates its immunomodulatory potential in mastitis.

• Journal of Acupuncture Research
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• 제32권3호
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• pp.15-25
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• 2015

Objectives : The purpose of this study is to investigate the effects of Pyrrosiae Herba herbal-acupuncture(PH-HA) at $KI_{10}$(Umgok) on nephritis induced by lipopolysaccharide(LPS) in rats. Methods : Rats were assigned to four groups: normal, LPS, saline and PH-HA. Rats in the saline and PH-HA groups were treated with saline injection and PH-HA respectively at $KI_{10}$, three times over the period of one week. All animals, except those in the normal group, were injected intra-peritoneally with LPS to induce nephritis. WBC, in blood, tumor necrosis factor alpha(TNF-${\alpha}$), cytokine-induced neutrophil chemoattractant 1(CINC-1), blood urea nitrogen(BUN), creatinine in serum, urinal volume, total protein creatinine in urine, and renal myeloperoxidase (MPO) were analyzed. Results : 1. PH-HA group showed significantly reduced levels of serum BUN, serum creatinine, TNF-${\alpha}$, and CINC-1 compared to the LPS group. Furthermore, a significant increase in urine output and more significant decreases in total protein in urine and MPO in renal tissue were observed in the PH-HA group when compared to the LPS group. 2. The PH-HA group showed significantly reduced levels of serum creatinine and renal MPO, and a more significant increase in urine output compared to the saline group. Conclusions : According to these results, it is postulated that PH-HA at $KI_{10}$ has anti-inflammatory and renal-protective effects on LPS-induced nephritis in rats, and both acupoint $KI_{10}$ and the herb Pyrrosiae Herba made contributions to these effects. Further studies on the interaction between acupoint $KI_{10}$ and the herb Pyrrosiae Herba may be needed.

• Journal of Veterinary Science
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• 제21권4호
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• pp.61.1-61.16
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• 2020

Background: Panax notoginseng saponins (PNS) are bioactive substances extracted from P. notoginseng that are widely used to treat cardiovascular and cerebrovascular diseases and interstitial diseases. PNS have the functions of scavenging free radicals, anti-inflammation, improving blood supply for tissue and so on. Objectives: The aim of this study was to investigate the effects of PNS on the oxidative stress of immune cells induced by porcine circovirus 2 (PCV2) infection in vitro and in vivo. Methods: Using an oxidative stress model of PCV2 infection in a porcine lung cell line (3D4/2 cells) and mice, the levels of nitric oxide (NO), reactive oxygen species (ROS), total glutathione (T-GSH), reduced glutathione (GSH), and oxidized glutathione (GSSG) and the activities of xanthine oxidase (XOD), myeloperoxidase (MPO) and inducible nitric oxide synthetase (iNOS) were determined to evaluate the regulatory effects of PNS on oxidative stress. Results: PNS treatment significantly reduced the levels of NO and ROS, the content of GSSG and the activities of XOD, MPO, and iNOS (p < 0.05), while significantly increasing GSH and the ratio of GSH/GSSG in infected 3D4/2 cells (p < 0.05).Similarly, in the in vivo study, PNS treatment significantly decreased the level of ROS in spleen lymphocytes of infected mice (p < 0.05), increased the levels of GSH and T-GSH (p < 0.05), significantly decreased the GSSG level (p < 0.05), and decreased the activities of XOD, MPO, and iNOS. Conclusions: PNS could regulate the oxidative stress of immune cells induced by PCV2 infection in vitro and in vivo.

• Tuberculosis and Respiratory Diseases
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• 제52권4호
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• pp.355-366
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• 2002

연구배경: 열 전처치는 조직 내에 열충격단백질의 생성을 유도하며 이러한 열 전처치가 내독소로 유도된 쥐의 급성폐손상을 감소시키고 패혈증에 의한 사망률을 감소시킨다고 알려져 있다. 그러나, 폐손상을 유발하는 원인에 노출된 후 가해진 열처치가 폐손상에 미치는 효과에 대하여는 아직까지 잘 알려져 있지 않다. 따라서 본 연구는 내독소 투여 직후 시행한 열충격이 내독소에 의해 유발된 쥐의 급성폐손상에 미치는 영향과 그에 따른 염증성 및 항염증성 사이토카인에 미치는 영항을 알아보고자 하였다. 방 법: 대조군은 백서의 기관지 내로 생리식염수를 투여하였고 열처치 대조군은 생리식염수 투여 직후 열처치를 시행하였다. 내독소군은 열처치 없이 내독소를 기관지내로 투여하였다. 열 전처치군은 내독소 투여 18시간 전에 열 전처치를 시행하였고, 열 동시처치 군은 내독소 투여 직후 열처치를 시행하였다. 내독소 투여 후 6시간에 기관지폐포세척을 시행하여 기관지폐포세척액 내의 호중구 백분율을 측정하였고 폐를 적출하여 myeloperoxidase(MPO)의 활성도를 측정하였으며 기관지폐포세척액과 혈청에서 LDH(lactic dehydrogenase), 단백질, IL(interleukin)-$1{\beta}$, TNF(tumor necrosis factor)-${\alpha}$ 및 IL-10를 측정하였다. 또한 각군에서 폐 조직 내 HSP72의 표현정도를 관찰하였다. 결 과: 1) 내독소군, 열 전처치군 및 열 동시처치군 모두에서 기관지폐포세척액 내의 호중구 백분율, 폐조직이 MPO, 혈청 및 기관지폐포세척액내의 $IL-1{\beta}$, $TNF-{\alpha}$ 및 IL-10이 대조군에 비해 증가하였다(각 p<0.05). 2) 열 동시처치군은 폐조직의 MPO와 기관지폐포세척액 단백질의 농도가 내독소군과 차이가 없었고 기관지폐포세척액의 LDH가 내독소군에 비해 증가하였다(p<0.05). 3) 열 동시처치군의 혈청 $TNF-{\alpha}$의 농도는 내독소군과 비교 시 증가하였다(p=0.01). 결 론: 내독소 투여 직후 시행한 열충격은 내독소로 유도되는 폐손상을 감소시키지 못하며 염증성 사이토카인의 농도를 증가시켰다.

• 한국식품영양과학회지
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• 제37권3호
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• pp.309-316
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• 2008

본 연구에서는 알코올을 이용하여 만성위궤양 실험동물 모델을 확립하고 설정된 동물모델을 대상으로 비타민 E 투여 수준(결핍 0 mg/mL oil/day, 정상 1 mg/mL oil/day, 보충 10 mg/mL oil/day)에 따른 위궤양 치유효과를 살펴보고자 수행되었다. 비타민 E를 투여시킨 기간은 총 7일로서 위의 조직학적 검사, 혈청의 gastrin 농도, 위 조직의 histamine 농도, 위 조직 내의 항산화 효소인 GPx 활성도와 catalase 농도 및 MPO 활성도를 측정하였으며 그 결과를 요약하면 다음과 같다. 만성군에서 식이섭취량과 15% 에탄올 식수섭취량에는 유의적인 차이가 없었으나 체중증가량은 비타민 E 결핍군에서 유의적으로 낮았다. 급성군에 비해 만성군에서 위 무게가 유의적으로 낮게 나타났다. 또한 급성군에서 다량의 출혈과 선상의 괴사가 나타났으며 비타민 E 결핍군 또한 약간의 출혈과 선상의 궤양이 남아있었으나 비타민 E 정상군과 보충군의 경우 출혈이나 궤양은 관찰되지 않았다. 혈청 gastrin의 경우 비타민 E 결핍군에서 유의적으로 높았으며 비타민 E 투여수준에 따라 유의적으로 낮아졌다. 또한 위 조직에서 histamine 농도는 급성군보다 만성군에서 유의적으로 높게 나타났지만 만성군에서 비타민 E의 투여수준에 따른 histamine 농도의 차이는 나타나지 않았다. 위 조직에서의 MDA 농도는 비타민 E 결핍군과 정상군에 비해 보충군에서 유의적으로 높게 나타났으며 급성과 만성유도에 따른 MDA 농도 차이는 관찰되지 않았다. 또한 대표적인 항산화 효소인 GPx와 catalase의 경우 비타민 E 정상군과 보충군에서 유의적으로 낮게 나타났다. 위 조직에서의 MPO 활성도는 비타민 E 결핍군에 비해 정상군과 보충군에서 유의적으로 낮게 나타났다. 결론적으로 알코올로 유도한 만성위궤양 실험동물 모델에서 비타민 E의 보충은 위궤양 치유효과가 있는 것으로 평가되었다. 비타민 E 보충은 혈청 gastrin 농도를 감소시켜 위에서의 산 분비를 감소시키며 또한 위 조직 내의 MPO 활성도를 감소시켜 proinflammatory cytokine을 방출을 억제시키고 결과적으로 위 세포내로의 호중구 침투를 감소시켜 위궤양 치유과정을 촉진시키는 것으로 보인다. 따라서 비타민 E의 결핍상태보다 비타민 E를 보충하였을 때 빠른 위궤양 치유효과가 있는 것으로 사료되며, 평소 권장량을 충족시킬 수 있는 비타민 E의 충분한 식이섭취가 중요하다고 생각한다.

• Korean Journal of Acupuncture
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• 제24권4호
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• pp.131-149
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• 2007

Objectives : The purpose of the present study is to evaluate the effects of herbal acupuncture (HA) with Moxi-tar for the treatment to intestinal disease in mice with 2, 4, 6 - trinitrobenzenesulfonic acid (TNBS) induced colitis. Methods : Mice were administered with 5% TNBS at day 1 and day 7. To investigate effects of HA with Moxi-tar at LI11, treatments were carried out at day -1, day 1, day 3, day 5, and day 7. It was checked on the weight and width of colon, diarrhea, edema, survival rate, changes of body weight, and myeloperoxygenase (MPO) activity. Furthermore, we carried out immunohistochemical staining and Western blot and analyzed mRNA expression by RT-PCR. Results : HA of Moxi-tar at LI11 in preventive mode suppressed macroscopic damages and damages of intestinal epithelial cells and infiltration of immune cells in the colon by TNBS. HA in early and preventive mode ameliorated various symptoms by TNBS. TNBS injection increased MPO activity in colon while HA in preventive mode suppressed increase of MPO activity. HA down-regulated NF-kB activity and reduced expression of TNF-a, IL-1b, and ICAM-1 in colon of TNBS treated mice. Similar to experiment at colon, HA down-regulated NF-kB activity and reduced expression of TNF-a, IL-1b, and ICAM-1 by TNBS in mesenteric lymph node. HA in therapeutic mode suppressed errosion and shortening of colon and MPO activity by TNBS and suppressed mRNA expression of TNF-a, IL-1b, and ICAM-1 in the colon. Conclusions : This study demonstrates that HA with Moxi-tar at LI11 represents a potential therapeutic method of inflammatory bowel diseases.

• 한국음향학회지
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• 제15권6호
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• pp.81-89
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• 1996

원전의 1차 계통 건전성 확보를 위한 일환으로서 초음파 검사 방법은 매우 중요하다. 그러나, 초음파는 검사 대상제의 내부 구조 및 형상에 따라 검사의 제한을 받으므로 결정립이 큰 재질에서 후방 산란 잡음 즉 시 불변성(time invariant) 잡음이 발생한다. 이로 인하여 수신 신호는 낮은 신호 대 잡음비의 결과로 나타나게 된다. 주파수 대역 분할 방식(split spectrum processing:SSP) 기술은 이와 같은 잡음을 억제하는데 효율적이다. 그러나, 종래의 SSP 기술은 minization, PT 알고리즘중 한 알고리즘만 적용하였으나 본 논문에서는 이두 가지 알고리즘을 동시에 처리하는 MPO(minimization and polarity threshold)알고리즘을 적용하고, 주파수 대 대역폭비가 일정한 FIR 여파기로서 새로운 constant-Q SSP를 수행하여 신호처리 시간을 단축하였다. 현장 검사 요건과 동일하게 종파와 횡파에도 일부 적용하였다. 한편, 이러한 새로운 SSP 기술을 적용할 수 있도록 초음파 탐상기를 설계 제작하였고, 시험편들의 준비는 원전 모재 대비시험편, 모재와 동일한 재질의 스테인레스 스틸 및 구리 시험편들이며, 이들 시험편으로 부터 초음파 신호를 수집하여 본 신호 처리를 적용한 결고 신호 대 잡음비가 향상됨을 알 수 있었다.

• The Korean Journal of Physiology and Pharmacology
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• 제4권3호
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• pp.219-226
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• 2000

In order to elucidate the role of platelet activating factor (PAF) in the acute lung injury induced by endotoxin (ETX), activities of phospholipase A2, lyso PAF acetyltransferase and oxidative stress by neutrophilic respiratory burst were probed in the present study. To induce acute lung injury, $100\;{\mu}g$ of E.coli ETX (type 0127; B8) was instilled directly into the tracheae of Sprague-Dawley rats. Five hours after the ETX instillation, induction of acute lung injury was confirmed by lung leak index and protein contents in the bronchoalveolar lavage (BAL) fluid. At the same time, lung phospholipase A2 (PLA2) activity and expression of group I and II secretory type PLA2 were examined. In these acutely injured rats, ketotifen fumarate, known as lyso PAF acetyltransferase inhibitor and mepacrine were administered to examine the role of PAF in the pathogenesis of the acute lung injury. To know the effect of the ETX in the synthesis of the PAF in the lungs, lyso PAF acetyltransferase activity and PAF content in the lungs were measured after treatments of ETX, ketotifen fumarate and mepacrine. In addition, the role of neutrophils causing the oxidative stress after ETX was examined by measuring lung myeloperoxidase (MPO) and enumerating neutrophils in the BAL fluid. To confirm the oxidative stress in the lungs, pulmonary contents of malondialdehyde (MDA) were measured. After instillation of the ETX in the lungs, lung leak index increased dramatically (p＜0.001), whereas mepacrine and ketotifen decreased the lung leak index significantly (p＜0.001). Lung PLA2 activity also increased (p＜0.001) after ETX treatment compared with control, which was reversed by mepacrine and ketotifen (p＜0.001). In the examination of expression of group I and II secretory PLA2, mRNA synthesis of the group II PLA2 was enhanced by ETX treatment, whereas ketotifen and WEB 2086, the PAF receptor antagonist, decreased the expression. The activity of the lysoPAF acetyltransferase increased (p＜0.001) after treatment of ETX, which implies the increased synthesis of PAF by the remodelling of lysoPAF in the lungs. Consequently, the contents of the PAF in the lungs were increased by ETX compared with control (p＜0.001), while mepacrine (p＜0.001) and ketotifen (p＜0.01) decreased the synthesis of the PAF in the lungs of ETX treated rats. The infiltration of the neutrophils was confirmed by measuring and enumerating lung MPO and the neutrophils in the BAL fluid respectively. Compared with control, ETX increased lung MPO and number of neutrophils in BAL significantly (p＜0.001) whereas mepacrine and ketotifen decrerased number of neutrophils (p＜0.001) and MPO (p＜0.05, p＜0.001, respectively). The lung MDA contents were also increased (p＜0.001) by ETX treatment, but treatment with mepacrine (p＜0.001) and ketotifen (p＜0.01) decreased the lung MDA contents. Collectively, we conclude that ETX increases PLA2 activity, and that the subsequently increased production of PAF was ensued by the remodelling of the lyso PAF resulting in tissue injury by means of oxidative stress in the lungs.

• Journal of Ginseng Research
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• 제38권1호
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• pp.8-15
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• 2014

Helicobacter pylori-induced gastric inflammation includes induction of inflammatory mediators interleukin (IL)-8 and inducible nitric oxide synthase (iNOS), which are mediated by oxidant-sensitive transcription factor NF-${\kappa}B$. High levels of lipid peroxide (LPO) and increased activity of myeloperoxidase (MPO), a biomarker of neutrophil infiltration, are observed in H. pylori-infected gastric mucosa. Panax ginseng Meyer, a Korean herb medicine, is widely used in Asian countries for its biological activities including anti-inflammatory efficacy. The present study aims to investigate whether Korean Red Ginseng extract (RGE) inhibits H. pylori-induced gastric inflammation in Mongolian gerbils. One wk after intragastric inoculation with H. pylori, Mongolian gerbils were fed with either the control diet or the diet containing RGE (200 mg RGE/gerbil) for 6 wk. The following were determined in gastric mucosa: the number of viable H. pylori in stomach; MPO activity; LPO level; mRNA and protein levels of keratinocyte chemoattractant factor (KC, a rodent IL-8 homolog), IL-$1{\beta}$, and iNOS; protein level of phospho-$I{\kappa}B{\alpha}$(which reflects the activation of NF-${\kappa}B$); and histology. As a result, RGE suppressed H. pylori-induced mRNA and protein levels of KC, IL-$1{\beta}$, and iNOS in gastric mucosa. RGE also inhibited H. pylori-induced phosphorylation of $I{\kappa}B{\alpha}$ and increases in LPO level and MPO activity of gastric mucosa. RGE did not affect viable H. pylori colonization in the stomach, but improved the histological grade of infiltration of poly-morphonuclear neutrophils, intestinal metaplasia, and hyperplasia. In conclusion, RGE inhibits H. pyloriinduced gastric inflammation by suppressing induction of inflammatory mediators (KC, IL-$1{\beta}$, iNOS), MPO activity, and LPO level in H. pylori-infected gastric mucosa.