• Asian-Australasian Journal of Animal Sciences
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• 제28권6호
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• pp.896-902
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• 2015

Milking center wastewater (MCW) has a relatively low ratio of carbon to nitrogen (C/N ratio), which should be separately managed from livestock manure due to the negative impacts of manure nutrients and harmful effects on down-stream in the livestock manure process with respect to the microbial growth. Simultaneous nitrification and denitrification (SND) is linked to inhibition of the second nitrification and reduces around 40% of the carbonaceous energy available for denitrification. Thus, this study was conducted to find the optimal operational conditions for the treatment of MCW using an attached-growth biofilm reactor; i.e., nitrogen loading rate (NLR) of 0.14, 0.28, 0.43, and $0.58kg\;m^{-3}\;d^{-1}$ and aeration rate of 0.06, 0.12, and $0.24\;m^3\;h^{-1}$ were evaluated and the comparison of air-diffuser position between one-third and bottom of the reactor was conducted. Four sand packed-bed reactors with the effective volume of 2.5 L were prepared and initially an air-diffuser was placed at one third from the bottom of the reactor. After the adaptation period of 2 weeks, SND was observed at all four reactors and the optimal NLR of $0.45kg\;m^{-3}\;d^{-1}$ was found as a threshold value to obtain higher nitrogen removal efficiency. Dissolved oxygen (DO) as one of key operational conditions was measured during the experiment and the reactor with an aeration rate of $0.12\;m^3\;h^{-1}$ showed the best performance of $NH_4-N$ removal and the higher total nitrogen removal efficiency through SND with appropriate DO level of ${\sim}0.5\;mg\;DO\;L^{-1}$. The air-diffuser position at one third from the bottom of the reactor resulted in better nitrogen removal than at the bottom position. Consequently, nitrogen in MCW with a low C/N ratio of 2.15 was successfully removed without the addition of external carbon sources.

• 한국양식학회지
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• 제19권1호
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• pp.25-32
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• 2006

본 연구는 상업적 규모의 대형 탱크에서 볼락 종묘 생산 기간 동안 사육 시스템 내 일어나는 수질 환경 변화를 알아보았다. 3개의 원형 수조(지름 6.5 m, 높이 2 m,수량 50톤)에 볼락 친어를 10마리씩(평균 무게 363.3 g, 수용밀도 $0.061kg/m^3$) 수용하여 종묘 생산을 하였으며, 실험 기간 동안 수온은 $14.2{\sim}16.1^{\circ}C$를 유지하였다. 먹이는 출산 1일부터 9일까지 로티퍼만, 출산 10일부터 20일까지 로티퍼와 알테미아를 병행하여, 출산 21일 부터 35일까지 알테미아만, 출산 36일부터 80일까지 알테미아와 배합 사료를 병행하여 그리고 출산 81일부터 조사가 끝난 85일까지 배합사료만 공급하였다. 종묘 생산 기간 동안과 각 먹이 공급에 따른 일간 수질 변화를 조사하기 위하여 용존 산소, pH, $NH_4^+-N,\;NO_2^--N,\;NO_3^--N$, 그리고 $PO_4^{3-}-P$ 농도를 조사하였다. 볼락 치어는 85일령에 0.88 g까지 성장하였고, 체중의 일간 성장률은 8.0%일이었다. 배합 사료 공급양이 많아질수록 사육수의 평균 용존 산소$(24.4{\sim}13.0mg/L)$와 pH $(8.1{\sim}7.4)$ 농도는 감소하였고, $NH_4^+-N\;(4.5\;to\;76.3{\mu}M),\;NO_2^--N\;(0.02\;to\;0.06{\mu}M),\;NO_3^--N\;(3.0\;to\;5.9{\mu}M)$, 그리고 $PO_4^{3-}-P\;(0.41\;to\;0.59{\mu}M)$ 농도는 지속적으로 증가하였다. 일간 $NH_4^+-N$ 농도 변화가 가장 컸으며, 로티퍼의 경우 $3.0{\mu}M$에서 $9.1{\mu}M$까지, 알테미아 경우 $16.13{\mu}M$에서 $45.8{\mu}M$까지, 그리고 배합 사료 공급시에는 $36.5{\mu}M$에서 $120.1{\mu}M$까지 상승하였다. 일간 수질 변화에 따른 용존 무기 질소(로티퍼; 7.0 g/일, 알테미아; 24.7 g/일, 배합 사료; 140.9 g/일)와 인(로티퍼; 0.7 g/일, 알테미아; 0.7 g/일, 배합 사료; 2.2 g/일) 배출량은 배합 사료 공급 시기에 유의적으로 높았다(P<0.05). 이와 같은 결과는 상업적 볼락 대량 종묘 시설에서 사육 시스템 내 수질 및 사육 관리를 위한 중요한 정보를 제공할 것이다.

• 공업화학
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• 제20권3호
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• pp.241-250
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• 2009

지난 수 년간 본 연구팀은 새로운 티탄염 응집제를 이용하여 폐수를 응집한 후 생산된 슬러지에서 산화티탄을 생산하는 연구를 진행하였다. 티탄염의 응집 효율은 일반적으로 많이 사용되는 철염과 알루미늄염 응집제와 비슷하였으며 슬러지를 소성하여 제조한 산화티탄은 상용 산화티탄보다 더 넓은 표면적과 높은 광촉매 활성을 나타내었다. 산화티탄의 광촉매 활성 향상과 pH를 높이기 위해 응집보조제로서 철, 알루미늄, 칼슘을 사용하여 광촉매 활성이 높은 Fe, Al, Ca 도핑 산화티탄을 제조하였다. 이 기술의 실제 적용 가능성을 확인하기 위하여 염색폐수 파일럿 장치에 적용한 결과, 우수한 유기물 제거 능력과 빠른 응집체 형성이 확인되었다. 염색폐수 슬러지에서 제조한 산화티탄은 높은 유기물 제거 광촉매 활성과 물 광분해에 의해 수소를 생성하였다. 티탄염 응집제와 슬러지에서 제조한 산화티탄의 독성을 D. magna로 조사한 결과, 낮은 독성을 확인할 수 있었다. 이 총설은 미래의 슬러지 재활용 기술로 높은 적용 가능성을 가지는 티탄염으로 제조한 산화티탄의 특성을 체계적으로 정리하였다.

• 한국수정란이식학회지
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• 제33권3호
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• pp.139-147
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• 2018

Somatic cell nuclear transfer (SCNT) is a useful biotechnological tool for animal cloning. Until now, SCNT has been inefficient, especially in dog. It is believed that an embryo developmental block in SCNT embryos is cause of low production efficiency. However, no studies have been performed on canines for embryo developmental block. In this study, we attempted to evaluate the beneficial role of EDTA in canine parthenogenic (PA) embryos development to overcome embryo developmental block. The PA embryos were divided into 0.01 mM EDTA treated and non-treated groups. Embryo developmental efficiency was measured by activating chemically parthenote. After EDTA induction, PA embryos were evaluated for embryonic development, Reactive Oxygen Species (ROS) activity, mitochondrial integrity, ATP production and genomic activation. The EDTA treated PA embryos showed significantly higher survival rate and improved cavity formation compared to non-treated. Furthermore, cytoplasmic ROS level was mitigated and mitochondrial membrane potential was found significantly higher in EDTA treated group followed by higher ATP production. Moreover, major embryonic genomic activation specific markers/factors were also elevated in EDTA treated group. Conclusively, we elucidated that EDTA showed substantially positive effect to overcome embryo developmental block in canine.

• Asian-Australasian Journal of Animal Sciences
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• 제27권5호
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• pp.635-647
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• 2014

Unfertilized oocytes age inevitably after ovulation, which limits their fertilizable life span and embryonic development. Rapamycin affects mammalian target of rapamycin (mTOR) expression and cytoskeleton reorganization during oocyte meiotic maturation. The goal of this study was to examine the effects of rapamycin treatment on aged porcine oocytes and their in vitro development. Rapamycin treatment of aged oocytes for 24 h (68 h in vitro maturation [IVM]; $44h+10{\mu}M$ rapamycin/24 h, $47.52{\pm}5.68$) or control oocytes (44 h IVM; $42.14{\pm}4.40$) significantly increased the development rate and total cell number compared with untreated aged oocytes (68 h IVM, $22.04{\pm}5.68$) (p<0.05). Rapamycin treatment of aged IVM oocytes for 24 h also rescued aberrant spindle organization and chromosomal misalignment, blocked the decrease in the level of phosphorylated-p44/42 mitogen-activated protein kinase (MAPK), and increased the mRNA expression of cytoplasmic maturation factor genes (MOS, BMP15, GDF9, and CCNB1) compared with untreated, 24 h-aged IVM oocytes (p<0.05). Furthermore, rapamycin treatment of aged oocytes decreased reactive oxygen species (ROS) activity and DNA fragmentation (p<0.05), and downregulated the mRNA expression of mTOR compared with control or untreated aged oocytes. By contrast, rapamycin treatment of aged oocytes increased mitochondrial localization (p<0.05) and upregulated the mRNA expression of autophagy (BECN1, ATG7, MAP1LC3B, ATG12, GABARAP, and GABARAPL1), anti-apoptosis (BCL2L1 and BIRC5; p<0.05), and development (NANOG and SOX2; p<0.05) genes, but it did not affect the mRNA expression of pro-apoptosis genes (FAS and CASP3) compared with the control. This study demonstrates that rapamycin treatment can rescue the poor developmental capacity of aged porcine oocytes.

• Asian-Australasian Journal of Animal Sciences
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• 제30권9호
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• pp.1245-1252
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• 2017

Objective: Phellodendron amurense (P. amurense) and Humulus japonicus (H. japonicus) are closely involved in anti-oxidative response and increasing antioxidant enzymes activities. However, the effects of their extracts on development of preimplantation bovine embryos have not been investigated. Therefore, we investigated the effects of P. amurense and H. japonicus extracts on developmental competence and quality of preimplantation bovine embryos. Methods: After in vitro fertilization, bovine embryos were cultured for 7 days in Charles Rosenkrans amino acid medium supplemented with P. amurense ($0.01{\mu}g/mL$) and H. japonicus ($0.01{\mu}g/mL$). The effect of this supplementation during in vitro culture on development competence and antioxidant was investigated. Results: We observed that the blastocysts rate was significantly increased (p<0.05) in P. amurense ($28.9%{\pm}2.9%$), H. japonicus ($30.9%{\pm}1.5%$), and a mixture of P. amurense and H. japonicus ($34.8%{\pm}2.1%$) treated groups compared with the control group ($25.4%{\pm}1.6%$). We next confirmed that the intracellular levels of reactive oxygen species (ROS) were significantly decreased (p<0.01) in P. amurense and/or H. japonicus extract treated groups when compared with the control group. Our results also showed that expression of cleaved caspase-3 and apoptotic cells of blastocysts were significantly decreased (p<0.05) in bovine blastocysts derived from both P. amurense and H. japonicus extract treated embryos. Conclusion: These results suggest that proper treatment with P. amurense and H. japonicus extracts in the development of preimplantation bovine embryos improves the quality of blastocysts, which may be related to the reduction of ROS level and apoptosis.

• 한국수정란이식학회지
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• 제30권4호
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• pp.289-298
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• 2015

Edaravone (Eda) is a potent scavenger of inhibiting free radicals including hydroxyl radicals ($H_2O_2$). Reactive oxygen species (ROS) such as $H_2O_2$ can alter most kinds of cellular molecules such as lipids, proteins and nucleic acids, cellular apoptosis. In addition, oxidative stress from over-production of ROS is involved in the defective embryo development of porcine. Previous study reported that Eda has protective effects against oxidative stress-like cellular damage. However, the effect of Eda on the preimplantation porcine embryos development under oxidative stress is unclear. Therefore, in this study, the effects of Eda on blastocyst development, expression levels of ROS, and apoptotic index were first investigated in preimplantation porcine embryos. After in vitro fertilization, porcine embryos were cultured for 6 days in PZM medium with Eda ($10{\mu}M$), $H_2O_2$ ($200{\mu}M$), and Eda+$H_2O_2$ treated group, respectively. Rate of blastocyst development was significantly increased (P<0.05) in the Eda treated group compared with only $H_2O_2$ treated group. And, we measured intracellular levels of ROS by DCF-DA staining methods and investigated numbers of apoptotic nuclei by TUNEL assay analysis is in porcine blastocyst, respectively. Both intracellular ROS levels and the numbers of apoptotic nucleic were significantly decreased (P<0.05) in porcine blastocysts cultured with Eda ($10{\mu}M$). More over, the total cell number of blastocysts were significantly increased (P<0.05) in the Eda-treated group compared with untreated group and the only $H_2O_2$ treated group. Based on the results, Eda was related to regulate as antioxidant-like function according to the reducing ROS levels during preimplantation periods. Also, Eda is beneficial for developmental competence and preimplantation quality of porcine embryos. Therefore, we concluded that Eda has protective effect to ROS derived apoptotic stress in preimplantation porcine embryos.

• Asian-Australasian Journal of Animal Sciences
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• 제31권9호
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• pp.1420-1430
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• 2018

Objective: Epigallocatechin-3-gallate (EGCG) is a major ingredient of catechin polyphenols and is considered one of the most promising bioactive compounds in green tea because of its strong antioxidant properties. However, the protective role of EGCG in bovine oocyte in vitro maturation (IVM) has not been investigated. Therefore, we aimed to study the effects of EGCG on IVM of bovine oocytes. Methods: Bovine oocytes were treated with different concentrations of EGCG (0, 25, 50, 100, and $200{\mu}M$), and the nuclear and cytoplasmic maturation, cumulus cell expansion, intracellular reactive oxygen species (ROS) levels, total antioxidant capacity, the early apoptosis and the developmental competence of in vitro fertilized embryos were measured. The mRNA abundances of antioxidant genes (nuclear factor erythriod-2 related factor 2 [NRF2], superoxide dismutase 1 [SOD1], catalase [CAT], and glutathione peroxidase 4 [GPX4]) in matured bovine oocytes were also quantified. Results: Nuclear maturation which is characterized by first polar body extrusion, and cytoplasmic maturation characterized by peripheral and cortical distribution of cortical granules and homogeneous mitochondrial distribution were significantly improved in the $50{\mu}M$ EGCG-treated group compared with the control group. Adding $50{\mu}M$ EGCG to the maturation medium significantly increased the cumulus cell expansion index and upregulated the mRNA levels of cumulus cell expansion-related genes (hyaluronan synthase 2, tumor necrosis factor alpha induced protein 6, pentraxin 3, and prostaglandin 2). Both the intracellular ROS level and the early apoptotic rate of matured oocytes were significantly decreased in the $50{\mu}M$ EGCG group, and the total antioxidant ability was markedly enhanced. Additionally, both the cleavage and blastocyst rates were significantly higher in the $50{\mu}M$ EGCG-treated oocytes after in vitro fertilization than in the control oocytes. The mRNA abundance of NRF2, SOD1, CAT, and GPX4 were significantly increased in the $50{\mu}M$ EGCG-treated oocytes. Conclusion: In conclusion, $50{\mu}M$ EGCG can improve the bovine oocyte maturation, and the protective role of EGCG may be correlated with its antioxidative property.

• 한국환경농학회지
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• 제20권1호
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• pp.44-49
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• 2001

식물의 대기오염 피해에 이차독성물질이 관여하는지를 조사하기 위하여 관엽식물 파키라(Pachira aquatica), 스파티필룸 (Spathiphyllum patinii) 및 헤데라(Hedera helix)에 $1\;{\mu}L/L$의 $SO_2$를 2일간 처리한 결과, 광합성 및 수분이용효율과 같은 생리활성 변화에 있어 파키라가 저감율이 가장 높았으며, 스파티필룸이 가장 낮게 나타났다. 가시피해 역시 파키라, 헤데라의 순으로 발현되었으며 스파티필룸에서는 가시피해가 나타나지 않아 $SO_2$에 대한 감수성이 파키라가 내성종, 스파티필룸이 민감종으로 대별되었다. 한편, 에틸렌과 활성산소 모두 $SO_2$ 처리에 의해 파키라에서 높게 유도되었으며 그 다음으로 헤데라, 스파티필룸의 순으로 나타나 $SO_2$에 대한 식물반응의 종간차이에 이차독성물질이 관여함을 알 수 있었다. 이같은 대기오염물질에 의한 식물체내 이차독성물질 생성은 대기오염에 대한 지표로서 이용될 수 있으며 이를 제어함으로서 피해의 진전을 저감시킬 수 있을 것으로 기대된다.

• The Korean Journal of Physiology
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• 제2권2호
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• pp.93-99
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• 1968

The Present study attempted to analyze the fate of CO diffused into the circulating blood through the alveoli. Dogs were induced to CO poisoning by rebreathing CO gas mixture contained in Krog's spirometer, by closed circuit method, for 60 minutes. The spirometer was filled initially with 282 ml of CO and 20 liters of air and oxygen, so the composition of gases were arranged as 1.4% in CO and 50% in $O_2$ at the begining of the rebreathing. Oxygen was added corresponding to the utilization of $O_2$ by the animal in proceeding of the experiment. At 60th minutes of CO rebreathing, the concentration of CO in arterial blood and in mixed venous blood were analysed and compared with each other after the CO contents were corrected with the hematocrit measured in the arterial and mixed venous blood. The distribution of CO gas to other tissues was estimated by the analysis of CO diffused into the cystic bile and into the peritoneal gas pocket which was formed by injection of 300 ml air into the peritoneal cavity prior to the CO gas rebreathing. The blood volume was measured by dilution method using $^{51}Chromium$ tagged red cells. CO amount vanished in the animal body was calculated by subtraction of total CO content in blood stream and the CO remained in closed circuit breathing system from the CO amount given to the breathing system at the begining of the experiment. Results obtained are summarized as follows: 1. The content of CO corrected by the hematocrit value was slightly less in mixed venous blood than in arterial blood. The amount of CO diffused into the cystic bile and into the peritoneal cavity was averaged to 0.1% and 0.4% of the CO amount in 100 ml of blood, respectively. 2. For 60 minutes of CO rebreathing, CO-hemoglobin saturation reached about 77% at the 60th minutes, CO amount vanished in the experimental animal averaged 36.1 ml/dog/hr., or 21% of the total CO volume in the blood stream. The average vanishing rate of CO during 60 minutes of CO rebreathing per kg of body weight was 2.71 ml/hr. Production of CO measured in ten dogs under hypoxic condition averaged 0.023 ml/kg/hr. The major part of the CO vanished in the dogs seemed to be oxidized to $CO_2$ by various tissues of the animal. The conclusion might be delivered as such oxidation of CO to $CO_2$ by animal tissues can play a role in part of the process of recovery and protection of animal from CO-poisoning.