• 제목/요약/키워드: fertilizing combination

검색결과 8건 처리시간 0.018초

Growth, Yield and Grain Quality affected by Seeding Rates and Fertilizing Combinations in Spring-sown Jinyangbori

  • Kim, Dae-Ho;Kim, Su-Kyeong;Kim, Eun-Seok;Song, Guen-Woo;Kang, Dong-Ju
    • 한국작물학회지
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    • 제45권2호
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    • pp.73-78
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    • 2000
  • This study was conducted for 2 years at Chinju region to establish suitable seeding rate and fertilizing levels of nitrogen, phosphorous and potassium in spring-sown Jinyangbori. Heading and maturing were delayed by increasing fertilizers, especially nitrogen. Number of spikes per were secured by much seeding and increased application of nitrogen. One thousand grain weight reduced with increasing fertilization at any seeding rate. Relatively high harvest indices were observed with 12-10-4 at 10kg. 10a$^{-l}$ seeds planted, followed by 6-10-8 at 15 kgㆍ 10a$^{-1}$, and 6-10-4kgㆍ 10a$^{-l}$ at 20kg ㆍ 10a$^{-l}$ of N-P-K fertilizing combinations, respectively. There was no distinct differences on yield for various seeding rates in spring-sown barley. When seeding rate increased up to 15kgㆍ10a$^{-1}$, the positive effect of fertilizers was recognized as the function of balanced-application. It was possible to recommend 10kgㆍ10a$^{-1}$ as seeding rate and 6-5-4(N-P-K)kgㆍ10a$^{-1}$ as fertilizing combination in spring-time seeding considering low input and sustainable agriculture. There was no significant difference of protein content in grain by seeding rate. Increase of nitrogen fertilizer enhanced protein content in grain.

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정자의 수정능력 평가기법 (In Vitro Assays of Sperm Fertility)

  • 박수봉
    • 한국수정란이식학회지
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    • 제10권1호
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    • pp.15-22
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    • 1995
  • Since the turn of the century, scientists have earnestly sought to develop a single laboratory assay or combination of laboratory assays which accurately predict the fertility of a semen sample. Most of these assays have focused on evaluating physical characteristics of sperm such as motility, viability, acrosomal integrity and morphology. In recent years new approches have been used to assess the functional aspects of a sperm that are needed to reach the oocyte, fertilize it and contribute to successful embryo development. Among these techniques are the ability of sperm to undergo a heparin induced acrosome reaction and in vitro fertilization, and the affinity of sperm to bind heparin binding protein. Intensification of research efforts in the area of control of sperm fertilizing ability should be a high priority, in view of undoubted benifits both to our basic understanding of sperm fertilizing ability and to our ability to modify it for Al industry.

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Glucose and Its Role in Generating Reactive Oxygen Species Required for Mouse Sperm Fertilizing Ability

  • Lin, S.C.;Chen, M.C.;Huang, A.J.;Salem, B.;Li, K.C.;Chou, K.
    • Asian-Australasian Journal of Animal Sciences
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    • 제13권6호
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    • pp.748-756
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    • 2000
  • Effects of xanthine (X), xanthine oxidase (XO), and catalase (C), $H_2O_2$, and carbohydrates on sperm capacitation, acrosome reaction, and fertilizing ability in vitro were examined. Glucose alone, but not fructose, supported the maximum rate of sperm capacitation and acrosome reaction. However, in the combination of X, XO, and C (XXOC) or $H_2O_2$, fructose alone also supported maximum capacitation, acrosome reaction, and fertilization. Either insufficient or excessive amounts of $H_2O_2$ decreased sperm capacitation and the acrosome reaction. In order to understand how glucose generates $H_2O_2$ or other reactive oxygen species in sperm cells, 6-aminonicotinamide, an inhibitor of the pentose-phosphate pathway (PPP), and apocynin, an inhibitor of NADPH oxidase, were added to sperm suspensions in glucose-containing medium. Results appeared that sperm capacitation, acrosome reaction, and fertilization were consequently inhibited by either one of these compounds. These inhibitory effects were nullified by addition of XXOC. These results support the hypothesis that glucose, in addition to being a substrate for glycolysis, facilitates sperm capacitation and the acrosome reaction by generating reactive oxygen species through G-6-P dehydrogenase and NADPH oxidase.

분변내 스테로이드 호르몬의 측정을 통한 멸종 위기 침팬지의 번식형태와 임상적용 (The Reproductive Patterns and Clinical Application of Endangered Common Chimpanzees by Monitoring the Steroid Hormone Measurements in Fecal Samples)

  • 정소영;김미영;정유정;장유니;임양묵;윤용달
    • 한국발생생물학회지:발생과생식
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    • 제15권2호
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    • pp.167-172
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    • 2011
  • 멸종 위기에 처한 침팬지에서 연중번식주기와 무월경, 번식주기, 임신진단을 포함한 번식형태를 관찰하기 위하여 형광항체 분석법을 사용하여 에스트라디올, 프로게스테론, 테스토스테론 호르몬 대사산물과 인간융모성 성선자극호르몬을 측정하였다. 본 연구결과, 침팬지의 번식능력은 연령이 번식에 중요한 영향을 주는 인자가 아니며, 개체별 번식능력의 차이, 산과질환의 유무, 배우자와 합사한 조건에서 나타나는 성적행동의 차이 같은 여러 가지 요인이 복합적으로 작용한다는 것을 알 수가 있었다. 본 연구는 침팬지의 종보전과 인간과 연관된 폐경과 산과질환을 연구하는데도 유용하게 활용될 수 있을 것이다.

ROLE OF REACTIVE OXYGEN SPECIES IN MALE INFERTILITY

  • Sharma, Rakesh K.;Agarwal, Ashok
    • 대한생식의학회:학술대회논문집
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    • 대한불임학회 2000년도 제39차 춘계 학술대회
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    • pp.13-28
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    • 2000
  • Human spermatozoa exhibit a capacity to generate ROS and initiate peroxidation of the unsaturated fatty acids in the sperm plasma membrane, which plays a key role in the etiology of male infertility. The short half-life and limited diffusion of these molecules is consistent with their physiologic role in key biological events such as acrosome reaction and hyperactivation. The intrinsic reactivity of these metabolites in peroxidative damage induced by ROS, particularly $H_2O_2$ and the superoxide anion, has been proposed as a major cause of defective sperm function in cases of male infertility. The number of antioxidants known to attack different stages of peroxidative damage is growing, and it will be of interest to compare alpha-tocopherol and ascorbic acid with these for their therapeutic potential in vitro and in vivo. Both spermatozoa and leukocytes generate ROS, although leukocytes produce much higher levels. The clinical significance of leukocyte presence in semen is controversial. Seminal plasma confers some protection against ROS damage because it contains enzymes that scavenge ROS, such as catalase and superoxide dismutase. A variety of defense mechanisms comprising a number of antioxidants can be employed to reduce or overcome oxidative stress caused by excessive ROS. Determination of male infertility etiology is important, as it will help us develop effective therapies to overcome excessive ROS generation. ROS can have both beneficial and detrimental effects on the spermatozoa and the balancing between the amounts of ROS produced and the amounts scavenged at any moment will determine whether a given sperm function will be promoted or jeopardized. Accurate assessment of ROS levels and, subsequently, OS is Vital, as this will help clinicians both elucidate the fertility status and identify the subgroups of patients that respond or do not respond to these therapeutic strategies. The overt commercial claims of antioxidant benefits and supplements for fertility purposes must be cautiously looked into, until proper multicentered clinical trials are studied. From the current data it appears that no Single adjuvant will be able to enhance the fertilizing capacity of sperm in infertile men, and a combination of the possible strategies that are not toxic at the dosage used would be a feasible approach.

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성선자극호르몬과 스테로이드호르몬의 첨가가 한우난포란의 체외성숙과 수정능력에 미치는 영향 (Effects of Gonadotropins and Steroid Hormones on Follicular Oocyte Maturation in Vitro and Fertilizing Ability In Vivo of Korean Native Cattle)

  • 박재원;김창근;정영채
    • 한국가축번식학회지
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    • 제11권1호
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    • pp.73-84
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    • 1987
  • This experiment was carried out to investigate the effects of hormone addition(FSH, HCG, estrogen and progesterone) and composition (BSA and FCS) of mKRB on the in vitro maturation and fertilizability of follicular oocytes of the Korean native cattle. The ovaries were removed at a slaughterhouse, returned to laboratory in a thermostat (30-35$^{\circ}C$) within 4 hr, and collected by aspirating normal follicles which had diameters of 1 to 6 mm. The oocytes with cumulus cells were cultured for 8, 16, 24 and 30 hr in a modified KRB solution containing BSA or FCS and hormones. The in vitro matured oocytes in mKRB containing FCS, FSH and steroids were transferred in the rabbit uterus for examination of their in vivo fertilizability with bovine sperm preincubated 4 to 6 hr in the rabbit uterus. 1. The mean number of oocytes collected per cattle was 6.5 from 1-3mm follicles, 1.3 from 4-6mm follicles, and total was 7.7. 2. The meiotic division at 16hr-cuture in the oocytes from 1-3mm follicles was slightly stimulated by the addition of FSH in mKRB + BSA solution compared with the control. At 30hr-culture, their maturation rates(%Met II) were also increased by FSH of 1 $\mu\textrm{g}$/ml(38.4%) and 5$\mu\textrm{g}$/ml(35.7%) as compared with the control (21.4%). The maturation rate at 30hr-culture in the oocytes from 4-6mm follicles was 53.8% and 57.1% by the FSH addition of 1$\mu\textrm{g}$/ml and 5$\mu\textrm{g}$/ml, respectively. These rates were similar with the control(57.1%), but higher than those of oocytes from 1-3mm follicles. 3. The meiotic division at 16hr-culture in the oocytes from 1-3mm follicles was stimulated by the HCG addition of 1IU/ml and 5IU/ml. However, the maturation rate at 30hr-culture was greatly decreased by the HCG addtion (26.6% and 13.3%) compared with the control(53.3%) and these rates (30.8%) in the oocytes from 4-6mm follicles were also lower than that fo the control(58.3%). 4. Low maturation rate (37.5%) of the oocytes cultured in mKRB containing BSA and 5IU/ml HCG was increased (55.0%) when 15% FCS with HCG was added to mKRB instead of BSA. 5. When 16hr-cultured oocytes in mKRB containing BSA and gonadotropins (5$\mu\textrm{g}$/ml FSH and 5IU/ml HCG) were transferred in the medium without gonadotropins and recultured for 16hr, the maturation rate of HCG-treated oocytes was greatly improved. 6. The maturation rates of oocytes were greatly affected by steroids. The combined addition of FCS+FSH+estrogen or +progesterone to mKRB increased the maturation rate compared with the combination of BSA+FSH or FCS+FSH in mKRB. 7. The fertilization rate, presence of pronuclei, was increased by the combination of FCS+FSH+p in mKRB as compared with that (5.6%) of BSA+FSH and the rates of FCS+FSH+steroids ranged from 12.5 to 17.6%.

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동결-융해 후 회수된 고환 정자와 세정관내 정자의 수정 능력과 효율성에 관한 연구 (Efficacy and Fertilizing Ability of Frozen-thawed Testicular Spermatozoa and Spermatozoa Extracted from the Seminiferous Tubule with Intracytoplasmic Sperm Injection (ICSI))

  • 박용석;전진현;이호준;강인수;김종현;이유식;서주태
    • Clinical and Experimental Reproductive Medicine
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    • 제25권2호
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    • pp.171-177
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    • 1998
  • The combination of testicular sperm extraction (TESE) with ICSI can achieve normal fertilization and pregnancy rate and is effective method in obstructive and non-obstructive azoospermic patients. But, when pregnancy was not occurred, repeated testicular biopsies are not evitable. Therefore, in this study, we observed the survival rate of testicular spemratozoa and spermatozoa extracted from the seminiferous tubules after cryopreserved-thawed used for next IVF cycle with ICSI. In a total of 23 cases, obstructive azoospermia was 17 cases and non-obstructive azoospermia was 6 cases. In obstructive azoospermia, after thawing, motile spermatozua was observed in 13 cases (76.5%). The fertilization rate with 2PN was 67.6% and 5 pregnancies (29.4%) were achieved. In non-obstructive azoospermia, motile spermatozoa was observed in 2 case (33.3%) after thawing. The fertilization rates with 2PN was 53.7% and 3 pregnancies (50.0%) were achieved. A comparison of the results of motile spermatozoa after thawed testicular spermatozoa and spermatozoa extracted from the thawed seminiferous tubule section were 3 cases (60.0%) and 12 cases (66.6%), respectively. The fertilization and pregnancy rates of thawed testicular spermatozoa and spermatozoa extracted from the thawed seminiferous tubule section were 69.4% and 20.0%, 62.5% and 38.8%, respectively. Conclusively, thawed testicular spermatozoa and spermatozoa extracted from the thawed seminiferous tubule section can achieve normal fertilization and pregnancy and cryopreservation of testicular spermatozoa and seminiferous tubule may avoid repetition of testicular biopsies in azoospermic patients in whom the only source of spermatozoa is the testis.

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비모란 선인장(Gymnocalycium mihanovichii var. 'Ihong') 시설재배에서 지렁이분변토시용에 따른 생육특성 및 토양 화학성 변화 (Changed in Growth and Chemical Properties of Plastic Film House by Earthworm Cast on Gymnocalycium mihanovichii var. 'Ihong')

  • 최이진;조상태;김영문;김미선;이상권
    • 한국유기농업학회지
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    • 제22권4호
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    • pp.731-742
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    • 2014
  • 본 연구는 다비 재배를 하고 있는 비모란선인장 재배토양에 친환경 부산물비료인 지렁이분변토를 혼합 재배할 때 구경, 구고, 자구수 및 토양 화학적 특성에 미치는 영향을 조사하여, 재배기간 동안 충분한 영양을 공급할 수 있고 생산량을 확보할 수 있는 적정 혼합비율을 규명하였다. 수출용 접목선인장인 비모란 선인장(대목: 9 cm 접수: $1.5{\times}1.3cm$ 접목묘) '이홍' 품종을 2013년 6월부터 12월까지 서울시 서초구 내곡동 서울특별시 농업기술센터 플라스틱하우스 내에서 수행하였다. 농가에서 재배하고 있는 모래와 비료를 50:50으로 혼합한 것을 대조구로 하고, 모래와 음식물쓰레기를 먹이로 하여 생산한 지렁이분변토의 혼합비율을 80:20, 60:40, 40:60, 20:80, 0:100으로 한 5조합의 pH는 7.1-7.4로 거의 비슷하게 조사되었는데 비모란선인장 재배의 적정 pH가 6.5-7.5로 적합한 범위였다. 유기물함량은 지렁이분변토 혼합비율이 높아짐에 따라 증가하였지만 관행처리구 55 mg/kg보다는 32-43 mg/kg으로 낮게 조사되었다. 치환성양이온함량은 혼합비율이 증가함에 따라 높아졌지만 관행처리구보다 $K^+$, $Na^+$, $Mg^{2+}$ 양이 적었으나 $Ca^{2+}$의 함량은 관행처리구는 $9.1cmol^+/kg$이나 지렁이분변토 혼합시 $11.5-33.7cmol^+/kg$으로 높게 조사되었다. 지렁이분변토 혼합비율에 따른 비모란선인장 이식 3개월 후 구경을 조사한 결과 대조구 31.39 mm 보다 지렁이분변토 혼합처리구가 32.46-37.59 mm로 유의성 있는 차이를 보였다. 이식 5개월 후 비모란선인장 생육특성을 조사한 결과 구경은 32.63 mm 보다 지렁이분변토처리구가 32.49-37.59 mm로 혼합비율이 증가함에 따라 유의성 있게 신장하였다. 구고는 대조구의 경우 2.63 mm이고 지렁이분변토 혼합비율에 따라 2.79-3.16 mm로 유의성 있게 조사되었다. 자구수가 많이 생기는 것은 농가에는 매우 유리한 상황인데 대조구는 2.7개이고 지렁이분변토 혼합비율이 높아짐에 따라 3.2-8.3개로 조사되어 고도로 유의하였다. 특히 지렁이분변토 80%와 100% 처리구에서 6.2개와 8.3개로 조사되어 대조구보다 2.5배 이상 증가하였는데 비모란선인장 재배농가에서 단기간 자구생산에 활용할 수 있을 것으로 사료되었다. 지렁이분변토 40%와 60% 혼합처리의 경우 자구수가 4.5와 4.8개로 대조구보다 많이 조사되었으며, 토양배수에도 문제가 없었고 이끼가 발생하는 현상도 없었다. 비모란선인장 생육특성을 조사해본 결과 지렁이분변토 40% 및 60% 혼합비율이 생육에 효율적이라고 판단되었다.