• The Korean Journal of Physiology
• /
• 제17권2호
• /
• pp.135-142
• /
• 1983

$PGE_2$ 및 $PGF_{2{\alpha}}$가 용혈 및 적혈구막 절편에서 $Ca^{++}$ 결합에 미치는 영향을 관찰하여 다음과 같은 결론을 얻었다. 1) $PGF_{2{\alpha}}$는 $PGE_2$와 같이 적혈구막 삼투성 취약성을 증가시키는데 대조군에서는 NaCl농도 1/18 M 용액에서 완전히 용혈되었으나 $PGE_2$ 및 $PGF_{2{\alpha}}$ 가 $10^{11}M$ 이상 포함될 경우 NaCl농도 $1/16{\sim}1/17\;M$ 에서 100 % 용혈이 일어났다. 2) 동일한 적혈구 부유액을 사용할 때 NaCl농도 1/15 M 용액에서 대조군은 $44.2{\pm}4.3%$가 용혈되나 $PGE_2$ 및 $PGF_{2{\alpha}}$가 $10^{11}M$농도로 포함되었을 때 용혈은 각기 $73.6{\pm}8.4%$ 및 $68.7{\pm}6.4%$로 대조군에 비하여 의의있게 증가하였으며 그 이상의 농도에서는 더 이상 증가를 보이지 않았다. 3) $PGE_2$ 및 $PGF_{2{\alpha}}$에 의해 증가된 용혈은 어느 $Ca^{++}$농도에서도 대조군보다 항상 일정한 정도로 증가되어 있다. 4) 적혈구막 절편에서의 $Ca^{++}$결합은 대조군이나 $PGE_2$ 및 $PGF_{2{\alpha}}$처치군 모두 incubation용액내 $Ca^{++}$농도가 증가함에 따라 곡선적으로 증가하여 $Ca^{++}$농도 5 mM에서 포화된다. 그러나 같은 농도의 $Ca^{++}$에서 비교할 때 적혈구막의 $Ca^{++}$결합은 $PGE_2$ 및 $PGF_{2{\alpha}}$ 존재시 대조군에 비하여 의의있게 증가되었다. 이상의 결과로 보아 $PGE_2$ 및 $PGF_{2{\alpha}}$가 적혈구막의 삼투성 취약성을 증가시키는 기전은 $Ca^{++}$과는 독립적으로 작용함을 알 수 있다.

• 한국수정란이식학회지
• /
• 제22권1호
• /
• pp.27-32
• /
• 2007

본 연구는 소 체외 수정란의 팽창 및 hatching시 prostaglandin $F_2{\alpha}(PGF_2{\alpha})$와 prostaglandin $E_2(PGF_2)$의 영향에 대하여 검토하였다. 체외 수정란의 체외 배양시 다음과 같이 (1) 0, 1, 10 및 100ng/ml $PGF_2{\alpha}$, (2) 0, 1, 10 및 100ng/ml $PGE_2$, (3) low $PGF_2{\alpha}$(1ng/ml : 1ng/ml), (4) low $PGF_2{\alpha}\;:\;high\;PGE_2(1ng/ml\;:\;10ng/ml)$, (5) high $PGF_2{\alpha}\;:\;low\;PGE_2$ (10ng/ml : 1ng/ml), (6) high $PGF_2{\alpha}$ : high $PGE_2$(10ng/ml : 10ng/ml)로 나누어 처리하였다. 그 결과, $PGF_2{\alpha}$ 및 $PGE_2$의 단독 처리가 소 체외 수정란의 배반포로의 발달에는 영향을 미치지는 않았다. 그러나 10ng/ml $PGE_2$(10.3%) 그리고 1ng/ml $PGF_2{\alpha}$ : 10ng/ml $PGE_2$(22.2%)를 처리한 수정란의 hatching율에 있어서는 대조군(4.3% and 12.7%)이나 다른 처리구에 비하여 유의적으로 높은 결과를 나타냈다(P<0.05). 한편 높은 농도의 $PGF_2{\alpha}$를 처리한 수정란의 경우 hatching율이 감소하였다. 따라서 본 연구의 결과는 $PGF_2{\alpha}$ 및 $PGE_2$의 첨가가 소 수정란의 hatching율과 관련이 있으며, 이것은 농도에 따라 서로 다른 영향을 미칠 수 있을 것으로 추측되었다.

• 생약학회지
• /
• 제37권4호
• /
• pp.283-289
• /
• 2006

Ethanol extracts of the whole herb of Agastachis Herba (A) and of Pueraria Radix (P) alone and of their mixture (A+P) downregulated the cell growth, cyclooxygenase-2 (COX-2) expression, prostaglandin $E_2\;(PGE_2)$, and cGMP production. A, P, and A + P inhibited the cell growth of HT-29 colon cancer cells in a concentration- and time-dependent manner but not the growth of normal colon cell, CCD-112CoN. In addition, they markedly inhibited the productions of $PGE_2$ and cGMP as well as the mRNA expression of COX-2. These data suggest that non-toxic concentration of A, P, and A + P have a significant effect on the in vitro growth of HT-29 cells, specifically through the inhibition of the $PGE_2$ production via COX-2.

• The Korean Journal of Physiology and Pharmacology
• /
• 제11권5호
• /
• pp.175-182
• /
• 2007

Members of prostaglandin(PG) E-series elicit cellular effects mainly through adenylyl cyclase-cAMP signaling. The role of $PGE_2$-induced increase in cAMP has been shown to be compartmentalized in the cardiac myocytes: $PGE_2$-induced increase of cAMP is not involved in the control of cardiomyocytic contraction. The purpose of the present study was to define the effect of $PGE_1$ on the cGMP levels and the role of $PGE_1$ in the atrial secretory function. Experiments were performed in perfused beating rabbit atria and atrial contractile responses, cGMP and cAMP efflux, and atrial natriuretic peptide(ANP) secretion were measured. $PGE_1$ increased cGMP as well as cAMP efflux concentration in a concentration-dependent manner, however, no significant changes in atrial secretory responses were observed(with $1.0{\mu}M\;PGE_1$; for cGMP, $144.76{\pm}37.5%$, n=11 versus $-16.81{\pm}4.76%$, n=6, control, p<0.01; for cAMP, $187.60{\pm}41.52%$, n=11 versus $7.38{\pm}19.44%$, n=6, control, p<0.01). $PGE_1$ decreased atrial dynamics slightly but transiently, whereas $PGE_2$ showed similar effects but with lower potency. Isoproterenol increased atrial cAMP efflux(with 2.0 nM; $145.71{\pm}41.89$, n=5 versus $7.38{\pm}19.44%$, n=6, control, p<0.05) and mechanical dynamics and decreased ANP secretion. The $PGE_1$-induced increase in cGMP efflux showed a bell-shaped concentration-response curve. $PGE_1$-induced increase of cGMP efflux was not observed in the presence of L-NAME, an inhibitor of nitric oxide(NO) synthase, or ODQ, an inhibitor of NO-sensitive guanylyl cyclase. L-NAME and ODQ showed no significant effect on the $PGE_1$-induced transient decrease of atrial dynamics. These data indicate that $PGE_1$ increases cGMP levels via NO-soluble GC signaling in the cardiac atrium and also show that $PGE_1$-induced increases in cGMP and cAMP levels are not involved in the regulation of atrial secretory and contractile functions.

• 약학회지
• /
• 제51권4호
• /
• pp.235-238
• /
• 2007

To determine the regulatory roles of phosphodiesterase (PDE) inhibitors on $PGE_2$-induced osteoclastogenesis, we investigated the effect of PDE inhibitors on osteoclast formation in the presence of $PGE_2$. Among PDE isozyme specific inhibitors, milrinone, a selective PDE3 inhibitor, and rolipram, a specific PDE4 inhibitor, increased $PGE_2$-induced osteoclast formation in cocultures of mouse bone marrow cells and osteoblasts. To verify that whether the PDE3 and PDE4 inhibitors act indirectly on osteoblasts, we measured the concentration of intracellular cAMP in osteoblasts. Treatment of milrinone or rolipram increased $PGE_2$-stimulated cAMP levels in osteoblasts. Furthermore, northern blot analysis revealed that the PDE3 and PDE4 inhibitors works synergistically with $PGE_2$ to increase the expression of TRANCE mRNA in osteoblasts. On the contrary, the PDE3 and PDE4 inhibitors did not augment the number of osteoclasts differentiated from bone marrow cells by $PGE_2$. In conclusion, the stimulation of $PGE_2$-induced osteoclast formation by the PDE3 and PDE4 inhibitors are attributable to their indirect effect on osteoblasts, not to their direct effect on bone marrow-derived osteoclast precursors.

• 대한약리학회지
• /
• 제25권1호
• /
• pp.93-99
• /
• 1989

본 교실의 연구결과에 의하면 토끼와 흰쥐에서 수정란 착상시기에 peripheral lymphocyte와 thymocyte의 활성도가 저하될 뿐만 아니라 착상기간중 생성되는 prostaglandin E(PGE)의 생리적인 농도로도 peripheral lymphocyte와 thymocyte의 활성도가 억제되었다. 그러므로 본 연구에서는 흰쥐의 착상시기에 전신적인 면역기능 뿐만 아니라 국소적으로 DLN lymphocyte의 활성도가 억제되는지를 관찰하고 PGE가 어떠한 기전으로 모체의 면역기능을 억제하는가를 관찰하여 다음과 같은 결과를 얻었다. 1. 흰쥐의 착상시기에 DLN lymphocyte의 활성도가 임신하기 않은 흰쥐의 DLN lymphocyte에 비하여 통계적으로 유의하지는 않으나 저하되었으며 이러한 저하현상은 100% 흰쥐에서 관찰되었다. 2. 착상시기의 DLN lymphocyte에 prostaglandin 합성억제제인 indomethacin(ID)를 처리하면 DLN lymphocyte의 활성도가 통계적으로 유의하게 증가하였다. 그러나 임신하지 않은 흰쥐의 DLN lymphocyte의 활성도는 증가되어 있으나 $PGE_2$를 전처리하면 DLN lymphocyte의 활성도가 유의하게 억제되며 $PGE_2$를 전처치한 후 ID를 처리하면 DLN lymphocyte의 활성도가 $PGE_2$로 전처치하지 않고 ID를 처리한 경우에 비하여 유의하게 증가하였다. 그러나 $PGE_2$ 대신estradiol, progesterone 및 hCG를 전처치하였을 경우에는 ID 처리로 DLN lymphocyte의 활성도가 증가하지 않았다. 3. 임신하지 많은 흰쥐의 DLN lymphocyte에 $PGE_2$를 전처리하면 PGE-producing cell이 유도되어 PGE 생성이 증가하는지를 확인하기 위하여 $PGE_2$를 전처리하고 Con A를 처리한 후 배양액의 PGE를 정량한 결과 PGE를 전처리하지 않은 DLN lymphocyte에 비하여 유의하게 PGE 생성이 증가하였다. 이상의 결과로 보아 흰쥐의 착상시기에는 모체의 DLN lymphocyte의 활성도가 저하되며, 특히 PCE는 PGE-producing cell을 유도함으로써 착상시기의 모체의 면역기능에 영향을 주는 것으로 생각된다.

• 한국발생생물학회지:발생과생식
• /
• 제15권1호
• /
• pp.17-24
• /
• 2011

Lipid metabolites involved in cellular regulation as signaling mediators. Prostaglandins (PGs), metabolites of lipid are involved to pregnancy at the time of implantation but the functional roles of PGs on embryo development are still controversy and largely unknown. In previous report, the levels of $PGE_2$ and $PGF_{2a}$ at embryos of morula stage and blastocyst stage were explored (Cheon et al., 1998). In this study, the previous suggestion was confirmed and the possible downstream mediator of prostaglandin $E_2$ and prostaglandin $F_{2a}$ on the expansion and hatching of mouse embryo was examined. As expected, developmental rate of the blastocyst to expanded stage was a concentration-response curve that showed the highest expansion rate at 10 ${\mu}M$ $PGE_2$, but at 100 ${\mu}M$ $PGE_2$, the rate was decreased. In contrast to the $PGE_2$, $PGF_{2a}$ stimulated expansion without toxicity at highest concentration. Cotreatment of PGs with indomethacin overcame the inhibitory effects of indomethacin in expansion. Exogenous PGs also improved the development of expanded embryos to the hatching stage. Besides, PGs receptors' transcripts detected at blastocyst. $PGE_2$ was caused of calcium fluctuation in the blastocyst but $PGF_{2a}$ did not. The changes of intracellular calcium concentration were different between indomethacin pretreated embryos and non-treated embryos. Based on these results it is suggested that PGs work as paracrine and/or autocrine factors through calcium and the others which were not identified in this study.

• 동의생리병리학회지
• /
• 제20권2호
• /
• pp.455-459
• /
• 2006

The inhibitors of prostaglandin $E_2\;(PGE_2)$ production and cyclooxygenase-2 (COX-2) activity have been considered as potential anti-inflammatory agents. In this study, we evaluated 9 compounds isolated from 5 Korean phytomedicinal plants (Spirea prunifolia, Paeonia suffruticosa, Salvia miltiorrhiza, Scutellaria baicalensis, and Artemisia capillaris) for the inhibition of $PGE_2$production and COX-2 expession in lipopolysaccharide (LPS)-stimulated human macrophages U937 cells. As a result, several compound such as prunioside A, penta-O-galloyl-beta-D-glucose, tanshinone IIA, baicalin, baicalein, wogonin, scopolatin, scoparone and decursinol showed potent inhibition of $PGE_2$production (50-70% inhibition at the test concentration of $10\;{\mu}M$). In addition, these compounds were also considered as potential inhibitors of COX-2 activity (45-73% inhibition at the test concentration of $10\;{\mu}M$). These active compound mediating COX-2 inhibitory activities are warranted for further elucidation of active principles for development of anti-inflammatory agents and these properties may contribute to the anti-atopic dermatitis activity.

• Journal of Radiation Protection and Research
• /
• 제12권2호
• /
• pp.9-18
• /
• 1987

천연 우라늄의 주독성이 중금속독성인지 혹은 방사성장해독성인지를 알기 위하여 질산납과 질산우라늄을 투여하여 변동되는 혈중 BUN, Creatinine, C-AMP 및 $PGE_2$의 활성도를 측정 비교하였다. 질산우라늄 투여시 비호소계인 질산대사의 임상적 지표인 BUN 및 Creatinine값은 질산납 투여군에 비교하여 예민한 반응을 나타났으나 C-AMP의 활성도에는 의의있는 변화가 없었다. 한편 질산 우라늄의 농도 변화에 따른 $PGE_2$ 활성도의 변동은 질산납 투여와 달리 현저하게 증가 되는 것을 관찰하였다. 이 결과는 천연우라늄의 저준위 방출 방사선이 세포막에 반응하여 $PGE_2$농도에 변화를 주는 것으로 사료된다. 질산 우라늄의 투여로 증가된 혈중 $PGE_2$의 농도를 감퇴시킴에 있어 Glucagon, Aldosterone 및 Furosemide를 사용하였다.

• 대한약리학회지
• /
• 제11권2호
• /
• pp.41-46
• /
• 1975

The isolated strips of tortoise intestine are evaluated as a test organ for bioassay of prostaglandin $E_1$. This preparation responded highly sensitively to $PGE_1$ and $PGE_2$ in picogram concentration range. The mean slope and the value of precision index among the doses of 0.1, 0.3 and 0.5ng/ml in final concentration were 37.7 and 0.143, respectively. And this was relatively insensitive to different prostaglandins; $E_1/E_2{\gtrsim}1$, $E_1/A_2{\sim}50$ and $E_1/F_{2\alpha}{\sim}100$, and showed the dual responses to 5-hydroxytryptamine and histamine; initial contraction followed by relaxation. The dose-ratio inducing the relative equal contraction height for $PGE_1$, acetylcholine, caerulein, angiotensin and barium chloride was 0.4 : 50 : 25 : 10 : 100 in this order. These results suggest that the intestinal strips of the tortoise are suitable for bioassay of prostaglandin $E_1$ and $E_2$ between the doses of 0.1 and 1.0 ng/ml level in the tissue extracts.