• Archives of Pharmacal Research
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• 제27권2호
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• pp.217-224
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• 2004

Previously, we reported that water-extracted Acanthopanax senticasus exhibited anti-meta-static activity by stimulating the immune system. In this study, we fractionated glycoproteins (EN-SP) from the soluble protein layer (GF-AS) of A. senticasus and determined their basic chemical properties. We also investigated the anti-tumor and immunostimulating activities of the fractionated glycoprotein, EN-SP. We found that intravenous (i.v.) administration of GF-AS dramatically inhibited metastasis of colon26-M3.1 carcinoma cells to the lung in a dose-dependent manner. In vitro analysis showed GF-AS to enhance the proliferation of splenocytes. GF-AS also stimulated peritoneal macrophage, which was followed by the production of various cytokines such as IL-1$\beta$, TNF-$\alpha$, IL-12 and IFN-${\gamma}$. Furthermore, the production of these cytokines was partially blocked when peritoneal macrophage was cultured with the polyclonal antibodies against GF-AS. The depletion of NK cells by rabbit anti-asialo GM1 serum partly abolished the inhibitory effect of GF-AS on lung metastasis of colon26-M3.1 cells. Using gel filtration, EN-SP, an active glycoprotein fraction, is isolated from GF-AS. While both GF-AS and EN-SP stimulated the proliferatation of splenocytes of normal mice, EN-SP showed higher anti-metastatic activity and more potently stimulated the proliferation of splenocytes compared to GF-AS. These results suggest the use of EN-SP, the fractionated glycoprotein from A. senticasus, can be used as a therapeutical reagent to prevent or inhibit tumor metastasis.

• 대한본초학회지
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• 제23권3호
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• pp.141-147
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• 2008

Objectives : The cortex and root of Acanthopanax sessiliflorus (AR), a herbal medicine, have been used for several diseases including cancer in Oriental countries. Recently, we reported that AR has an immune-potentiating action. Oga-Power(OP) was made using extract from AR. For these reasons, we hypothesized that OP can potentiate the immune system in terms of accelerating proliferation rates of immune cells such as thymocytes and splenocytes. Methods : In this experiment, proliferation rates of thymocytes and splenocytes were measured using modified 3-[4,5-dimethy -lthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT). No production levels in macrophages isolated from normal mice were measured using Griess method. Results : In our results, treatment with OP accelerated proliferation rates of splenocytes, but did not affect those of thymocytes in vitro. On the other hand, proliferation rates of thymocytes was elevated in vivo. In addition, level of NO production from macrophage separated from abdominal cavity of normal mice was elevated by treatment with OP. Conclusions : In conclusion, OP has immune-potentiating action, by acceleration of splenocyte proliferation and elevation of NO production level from macrophages.

• Environmental Analysis Health and Toxicology
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• 제22권3호
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• pp.263-269
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• 2007

Chitosan is a depolymerized and partially deacetylated derivative of chitin. We investigated the cytotoxicity of chitosan in cancer cell lines, such as P388, L1210, HCT-15, SK-HepG-1 and mouse splenocytes as a normal cell by MTT assay. To clarify whether chitosan enhances cytotoxicity of anticancer drugs, we also examined the cytotoxicity of combined treatment with chitosan and anticancer drugs, such as cisplatin, mitomycin C, and 5-fluorouracil in cancer cell lines in vitro. Chitosan ($37.5\;{\mu}g/mL,\;75\;{\mu}g/mL,\;112.5\;{\mu}g/mL,\;and\;150\;{\mu}g/mL$) showed concentration-dependent cytotoxicity in the cancer cell lines. In addition, chitosan showed relatively lower cytotoxicity in normal cells than in the cancer cell lines. Particularly, this trend was significant at high doses of chitosan, i.e. $112.5\;{\mu}g/mL,\;and\;150\;{\mu}g/mL$. Thus, these results suggest that chitosan may selectively induce the growth inhibition in cancer cell lines, compared to normal cells. Furthermore. the co-treatment of chitosan and anticancer drugs exhibited an apparant synergistic cytotoxicity in murine lymphoma cell lines, i.e. P388 and L1210 at $37.5\;{\mu}g/mL$ of chitosan rather than at $75\;{\mu}g/mL$ of chitosan, but such phenomenon could not be observed in solid tumor cell lines, i.e. HCT-15 and SK-HepG-1. However, chitosan did'nt reduced the cytotoxicity against normal mouse splenocytes induced by anticancer drugs. Therefore, it is concluded that the combination of chitosan and anticancer drugs might be useful for the cancer chemotherapy.

• 생명과학회지
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• 제17권5호
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• pp.694-698
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• 2007

본 연구에서는 berberine이 세포성 면역에 미치는 효과를 보기위하여 림프구증식과 GM-CSF생성을 보고자 하였다. 마우스 비장세포에 berberine을 작용시켰을 때 저농도에서 세포성장을 촉진함으로서 림프구증식에 자극제로서의 역할을 담당할 것으로 보인다. GM-CSF의 생성은 berberine 단독처리에 의해서 증가됨으로서 GM-CSF생성의 증가로 인한 세포성 면역반응의 상승이 예상되고 LPS나 Con A에 의한 GM-CSF의 생성을 저해함으로서 과도한 GM-CSF생성을 중간에서 차단할 것으로 보인다. 따라서 이러한 결과들은 앞으로의 추가적인 연구결과들이 있게 되면 임상에서의 면역요법과 항염증작용에 berberine이 이용될 가능성을 시사한다 하겠다.

• 방사선산업학회지
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• 제7권2_3호
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• pp.161-166
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• 2013

The purpose of this study was to investigate the cell proliferating and interleukin-2 producing activity of staphylococcal enterotoxin B by gamma-irradiation. Staphylococcal enterotoxin B was gamma-irradiated with the various doses of 0, 2, 20 and 50 kGy. SDS-PAGE analysis showed that gamma-irradiation caused the sharp decrease of the content of staphylococcal enterotoxin B and the effect was irradiating dose-dependent. Non-irradiated staphylococcal enterotoxin B increased the cell proliferation of splenocytes isolated from female Balb/c mouse, whereas 2 kGy-irradiated toxin significantly decreased the activity. 20 and 50 kGy-irradiated staphylococcal enterotoxin B was no effect. A similar effect on the interleukin-2 production of mouse splenocytes was observed with non-irradiated and irradiated staphylococcal enterotoxin B. It was considered to be due to the decrease of the antigenicity of staphylococcal enterotoxin B by gamma-irradiation. Therefore, these results suggest that gamma-irradiation can be effective for the decrease of the antigenicity of staphylococcal enterotoxin B as superantigen.

• Nutrition Research and Practice
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• 제17권2호
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• pp.206-217
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• 2023

BACKGROUND/OBJECTIVES: The immunomodulatory effect of Platycodon grandiflorum (PG) has been reported, but studies on its mechanism are still lacking. This study was undertaken to confirm whether the hydrolyzed and fermented PG extract (HFPGE) obtained by adding hydrolysis and fermentation to the extraction process has an immune-enhancing effect in the in vivo system. MATERIALS/METHODS: Five-week-old BALB/c mice were divided into 4 groups: normal control group (NOR), control group (CON), 150 mg/kg body weight (BW)/day HFPGE-treated group (T150), and 300 mg/kg BW/day HFPGE-treated group (T300). The mice were administered HFPGE for 4 weeks and intraperitoneally injected with cyclophosphamide (CPA, 80 mg/kg BW/day) on day 6, 7, and 8, respectively, to induce immunosuppression. The levels of immunoglobulins (Igs) and cytokines were measured in the serum. In splenocytes, proliferation and cytokine levels were measured. RESULTS: Serum IgA, IgG, and IgM levels were observed to decrease after CPA treatment, which was recovered by HFPGE administration. The levels of serum interleukin (IL)-12, tumor necrosis factor (TNF)-α, IL-8, and transforming growth factor (TGF)-β were also decreased after exposure to CPA but increased after HFPGE administration. Decreased splenocyte proliferation was seen in CPA-treated mice, but was observed to increase in the T150 and T300 groups as compared to the NOR group. Compared to the CON group, splenocyte proliferation stimulated with concanavalin A (ConA) or lipopolysaccharide (LPS) in the HFPGE-treated groups was significantly increased. The cytokines secreted by ConA-stimulated splenocytes (IL-2, IL-12, interferon-γ, TNF-α) were increased in the T150 and T300 groups, and cytokines secreted by LPS-stimulated splenocytes (IL-4, IL-8, TGF-β) were also increased by HFPGE administration. CONCLUSION: These results suggest that HFPGE stimulates the immunity in immunosuppressed conditions, thereby enhancing the immune response. Therefore, it is expected that HFPGE has the potential to be used as functional food and medicine for immune recovery in various immunocompromised situations.

• 한국응용과학기술학회지
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• 제40권5호
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• pp.955-964
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• 2023

Bee pollen is a valuable apitherapeutic product and has been known to have diverse biological activities, including antimicrobial, anti-inflammatory, and even anticancer activity. However, its effect on the immune system is not well studied and is rather controversial. This study intended to elucidate the biological activity of bee pollen on immunity. For this purpose, we used lyophilized bee pollen after wet grinding, which shows increased extraction of bioactive components and enhanced biological activity. First, lyophilized bee pollen after wet grinding significantly increased the proliferation of splenocytes isolated from normal mice. On the other hand, lyophilized bee pollen after wet grinding dose-dependently reversed splenocyte proliferation by concanavalin A or lipopolysaccharide. To clarify the activity of bee pollen on immunity lyophilized bee pollen after wet grinding was administered daily to mice for five weeks and isolated splenocytes. In this study, there was no significant difference in the population of immune cells and the size of spleen between bee pollen- and sterile water-treated groups. However, proliferation of splenocyte isolated from bee pollen-administered animals was boosted by both concanavalin A and lipopolysaccharide. Finally, kaempferol, a well-known flavonoid from bee pollen, dose-dependently increased splenocyte proliferation by both Con A and LPS. On the other hand, naringenin, another flavonoid in the bee pollen, dose-dependently inhibited the proliferation of splenocytes by Con A and LPS. Together, these data indicate that bee pollen may be able to prime the immunity to boost immune reaction after inflammation.

• 대한한방종양학회지
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• 제3권1호
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• pp.129-147
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• 1997

현재 서양의학에서 활용되고 있는 항암 요법으로는 외과처치(外科處置), 화학요법(化學療法), 방사선요법(放射線療法) 및 면역요법(免疫療法) 등(等)이 있으며, 그 중에서도 항암제(抗癌劑)에 의한 화학요법과 방사선요법이 가장 많이 응용되고 있다. 그런데 이들은 암세포(癌細胞)뿐만 아니라 정상세포(正常細胞)까지도 살상(殺傷)함으로써 종양세포(腫瘍細胞)를 억제하는 동시에 골수조혈기(骨髓造血器), 소화계통(消化系統) 및 면역기능(免疫機能)을 포함하는 인체의 정상적인 기능을 손상시키는 문제점으로 그 사용에 제한을 받고 있다. 따라서, 본 연구는 삼용부정탕(蔘茸扶正湯)의 항암요법으로 손상된 조직의 회복 및 조혈촉진 효과를 규명하기 위해 생쥐를 대상으로 하여 실험하였다. 그 결과, 생쥐 비장세포에 대한 증식효과(增殖效果), 조혈촉진인자(造血促進因子)의 분필능(分泌能), 방사선에 대한 임파구의 방어효과(防禦效果), 방사선에 대한 조혈세포 방어효과(防禦效果), 방사선(9Gy)을 조사받은 생쥐의 생존율(生存率) 등에서 유의성 있는 결과를 얻어내어 아래와 같이 보고하는 바이다.

• Journal of Animal Science and Technology
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• 제49권2호
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• pp.213-224
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• 2007

급성기 반응중인 가금의 비장세포와 PBMC 증식도를 alamar blue(alamar blue) 환원량으로 측정하기 위한 조건들을 조사하였다. 갓 부화한 육계병아리(Ross 종) 수컷에 기초사료를 급여하고, 9, 11 및 13일령에 각각 복강내 LPS를 주입으로 급성기 반응중인 14일령 육계병아리의 혈액에서 PBMC와 비장에서 비장세포를 분리하였다. alamar blue 환원량은 비장세포에서는 4, 24, 48, 96 및 120시간, PBMC는 4, 8, 12, 24 및 48시간에 그리고 웰당 103, 104 및 105개로 분배하고, 배양액 ml 당 0.0, 1.0, 5.0 및 10.0㎍의 Con A를 첨가하며, 배양액 중 2.5%의 자가혈청과 FBS를 첨가하여 측정하였다. 1.alamar blue 환원량은 배양시간의 경과(R2=0.825~1.000)에 따라 그리고, 세포수(R2= 0.999)의 증가에 따라 직선적으로 증가하였다.2. 급성기 반응중인 병아리에서, alamar blue 환원량은 대조구에 비해 비장세포는 24시간이후, PBMC는 4시간이후부터 105개의 세포접종시 유의하게(p<0.05) 높았다.3.급성기 반응중인 병아리의 비장세포와 PBMC에서 alamar blue 환원량은 Con A 농도에 관계없이 대조구에 비해 높았으며, 배양액 ml 당 Con A 1.0 또는 5.0 ㎍ 첨가에 비해 10.0㎍ 첨가시 유의하게(p<0.05) 높았다.4. 그리고, 배양액중 2.5%의 자가혈청은 급성기 반응과 관계없이 FBS에 비해 alamar blue 환원량을 유의하게 높였다. 본 연구는 alamar blue 환원량 평가에 의한 급성기 반응중인 가금의 비장세포와 PBMC의 증식도 측정에는 alamar blue 첨가 후 PBMC는 4시간, 비장세포는 24시간 배양, 세포수는 웰 당 105개, 그리고, Con A는 배양액 ml 당 10.0 ㎍이 적당하다는 것을 나타낸다.

• 한국식품영양과학회지
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• 제34권2호
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• pp.167-175
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• 2005

본 연구는 우리나라 야산에서 손쉽게 구할 수 있는 구황식물인 어성초를 이용하여, 시험관 내 실험 및 생체 내 실험을 실시하여 어성초의 면역증강제로서 가능성을 살펴보았다. 시험관 내 실험에서는 건조시켜 분쇄한 어성초를 메탄올로 추출한 후 극성에 따라 핵산, 클로로포름, 에틸아세테이트, 부탄올, 물 순으로 계통추출하여 비장세포 증식능과 복강대식세포에 의한 사이토카인 분비능을 측정하였다. 그 결과, 비교적 극성이 높은 부탄을 분획물과 물 분획 물 첨가시에 비장세포 증식능이 250 $\mu\textrm{g}$/mL의 농도군에서까지 향상됨을 볼 수 있었다. IL-1$\beta$와 TNF- $\alpha$는 클로로포름과 물 추출물을 첨가했을 때 대조군에 비해 유의적으로 많은 양이 분비되었고, IL-6 는 에틸아세테이트, 부탄올, 물 층에서 대조군에 비해 유의적으로 향상되었다. 이들 세가지 사이토카인의 분비 수준은 모두 B 림프구를 자극하는 미토젠인 LPS보다는 높았으므로, B 림프구 자극 효과가 우수함을 확인할 수 있었다. 시험관 내 실험의 결과를 토대로 하여 2주간 격일로 어성초 열수 추출물을 마우스에게 직접 경구 투여하고 비장세포 증식능과 활성화된 복강 대식세포에 의한 염증성 사이토카인(IL-l$\beta$, IL-6, TNF- $\alpha$)의 분비량을 측정하였다. 그 결과 비장세포 증식능은 ConA와 LPS로 처리시 어서초 추출물을 500 mg/kg bw 농도로 투여 한 군에서 각각 최대의 비장세포 증식을 보였다. 활성화된 복강 대식 세포에 의한 사이토카인 분비량을 측정한 결과 500 mg/kg bw와 1000 mghg bw의 농도로 투여시 대조군에 비해 유의적으로 많은 양의 IL-6를 분비하였고, 500 mg/kg bw 투여군에서 대조군에 비해 많은 양의 TNF-$\alpha$를 분비하였다. 그러나, IL-1$\beta$의 분비량은 대조군에 비해 오히려 급격히 감소하는 것으로 나타나 어성초의 투여가 IL-$\beta$ 분비를 자극하지는 못하는 것으로 나타났다. 따라서 어성초 열수 추출물을 생체내에 적용시켰을 때 비장세포의 증식을 유도하고 복강 대식세포를 활성화시켜 IL-6와 TNF- $\alpha$의 분비를 촉진시키는 효과가 있는 것으로 나타났으며 , 적정 양은 500 mg/kg bw 정도인 것으로 사료된다. 비장세포 증식능과 복강 대식 세포 활성화를 통한 연구 결과에 의하면 어성초는 비교적 극성이 높은 용매에 용해되는 부분에 면역증강효과가 있는 물질이 함유되어 있는 것으로 판단된다. 따라서, 앞으로는 그 성분에 대한 순수 분리 및 이를 동정하는 연구가 계속적으로 이루어져야 할 것으로 보이고, 이는 식품소재개발에 있어서 중요한 기초 자료가 될 것으로 보인다.