• 수산해양기술연구
• /
• 제40권1호
• /
• pp.29-36
• /
• 2004

선망의 침강 저항 특성을 해명하기 위한 기초 연구로서, 망지의 재료가 다르고 침자량이 동일한 선망 모형의 침강특성을 해석하였다. 실험에 사용한 선망은, 그물실의 직경 및 발의 길이가 같은 폴리프로피렌系 (밀도 0.91g/cm$cm^3$), 폴리아미드系 (밀도 1.14g/cm$cm^3$) 및 폴리에스터系 (밀도 1.38g/cm$cm^3$)의 매듭 없는 망지를 사용하여, 뜸줄의 길이 420cm, 그물의 폭 86cm가 되도록 제작하였다. 이 그물들의 발줄에 침자를 25g, 45g, 60g 의 3 단계로 바꾸어 9종류의 모형그물을 만들고, 각각 PP-25, PA-25, PES-25, PP-45, PA-45, PES-45, PP-60, PA-60 및 PES-60그물이라고 이름을 붙였다. 회류수조의 수로 위에 투망장치를 설치해서 정지 상태의 수중에 투망하고, 관측부 전면에 설치한 비디오 카메라를 이용하여 촬영 녹화하였다. 그리고, 그물에 표시한 측정점의 좌표를 화상해석장치로 읽고 실험치를 구하였다. 여기서, 선망의 수직방향의 침강운동을 나타낸 이론식을 이용하여 수치해석을 행하였는데, 그 결과는 다음과 같다. 1. 침자량이 60g일 때, 아랫자락의 평균 침강속도는 PES그물 12.2 cm/sec로 가장 빠르고, PA그물 11.4 cm/sec, PP 그물 10.7cm/sec 순으로 늦게 나타났다. 2. 망지의 저항계수 $K_D$는, 계산결과 $K_D=0.09(\frac{\rho}{\rho_w})^4$의 관계식으로 나타낼 수 있었다. 3. 그물다발의 저항계수 $C_R$은, 계산결과 $C_R=0.91(\frac{\rho}{\rho_w})$의 관계식으로 나타낼 수 있었다. 4. 선망 투망후 경과시간에 따른 그물 아랫자락의 도달수심에 대한 실험치와 계산치의 관계는 상관성이 매우 높아, 침자량이 25g일 때 meas.=1.04 cal., 45g일 때 meas.=0.99cal.였으며, 60g일 때 meas.=0.98cal.의 관계를 나타냈다.

• Archives of Pharmacal Research
• /
• 제16권2호
• /
• pp.114-117
• /
• 1993

Ginsenosides present in the roots of panax ginseng C.A. Meyer were shown to induce a stimulatory effect on the overexpressed cellular chicken c-src protein tyrossine kinase in NH3T3 cells. Among 4 ginsenosides studied $(G-Rb_2,\;G-Rc,\;G-Re\;and\;G-Rg_1),\;G-Rg_1$ showed the most stimulatory effect at $16.7\mu{g/ml}$ ginsenoside concentration increasing the activity by 2-4 times. Inhibitors of either protein synthesis or RNA synthesis blocked the activation of c-src proein tyrosine kinase. These results suggest that the csrc kinase activation apprars to involve an increase in the amount of protein of the kinase by transcriptional control mechanism rather than an increase in the kinase activity.

• 한국가축번식학회지
• /
• 제21권3호
• /
• pp.293-302
• /
• 1997

Follicular oocytes of Grade I and II were collected from 2~6 mm ovarian follicles and matured in vitro (IVM) for 24 hrs in TCM-199 su, pp.emented with 35$\mu\textrm{g}$/ml FSH, 10$\mu\textrm{g}$/ml LH, and 1$\mu\textrm{g}$/ml estradiol-17$\beta$ at 39$^{\circ}C$ under 5% CO2 in air. They were fretilized in vitro (IVF) by epididymal spermatozoa capacitated with heparin for 12 hrs. The zygotes were then co-cultured in vitro with bovine oviducted epithelial cells (BOEC) for 7 to 9 days. The optimal time for IVM, the successful enucleation of IVM oocytes by micromanipulation at different oocyte ages after IVM, and the ideal culture system for IVM for effective IVF and in vitro development of IVM-IVF embryos was examined for in vitro production of nuclear recipient oocytes and nuclear donor embryos. To improve the efficiency of nuclear transplantation (NT) of IVF embryo into IVM follicular oocytes, this study evaluated the optimal electric condition and oocytes age for activation of IVM oocytes and in vitro development of NT embryos. In vitro development of NT embryos with preactivation or non-preactivation in enucleation oocytes, cell number of IVN-IVF embryos, and NT embryos wre also examined. The results obtained were as follows; 1. The most suitable enucleation time was at 24 hpm (83.3%) rather than that of 28 hpm(69.6%) and 32 hpm(50.0%). 2. There was no difference among the fusion rates of NT embryos at the voltages of 0.75, 1.0 and 1.5 kV/cm, but the in vitro development rates to morule and blastocyst were significantly (P<0.05) higher at the voltage of 0.75(12.5%) and 1.0kV/cm (12.6%) compared to 1.5kV/cm(0%). 3. No significant difference in activation rates were seen in NT embryos stimulated for 30, 60 and 120 $\mu$sec (71.7, 85.2 and 71.9%, respectively), but the in vitro development rates to morulae and blastocyst were significantly (P<0.05) higher in the oocytes stimulated for 30 $\mu$sec (11.6%) and 60 $\mu$sec(10.7%) than 120 $\mu$sec(0.0%). 4. The fusion rates (71.0 and 87.3%) and the in vitro development rates (9.1 and 12.7%) to morula and blastocyst were seen in the NT embryos stimulated at 28 and 32 hpm under the condition of 1.0 kV/ml, 60 $\mu$sec. However, at 24 hpm the fusion rates were 64.8% and the in vitro development to morula and blastocyst were not seen. 5. The fusion rates between the 8~12, 13~17 and 18~22-cell stage of IVM-IVF embryos were not significantly different. The in vitro development rates of the fused embryos to morula and blastocyst which were received from a blastomere of 8~12, 13~17 and 18~22-cell stages of IVM-IVF embryos were 14.9, 8.3 and 6.5%, respectively. 6. The in vitro development rate of the enucleated recipient oocytes with preactivation (24.2%) to morula and blastocyst was significantly (P<0.05) higher than that of non-preactivation (12.8%). 7. The cell numbers of NT blastocyst and IVM-IVF blastocyst cultured during 7~9 days were 63$\pm$11 and 119$\pm$23, and then their the mean cell cycle number were 5.98 and 6.89, respectively.