• 제목/요약/키워드: lymphocytes proliferation

검색결과 249건 처리시간 0.027초

김치의 급여가 흰쥐의 체내 지질함량과 비장 면역세포 증식능력에 미치는 영향 (The Effects of Kimchi Intake on Lipid Contents of Body and Mitogen Response of Spleen Lymphocytes in Rats)

  • 김지연;이연숙
    • 한국식품영양과학회지
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    • 제26권6호
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    • pp.1200-1207
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    • 1997
  • Effects of kimchi on lipid metabolism and immune function were studied in experiments using 63mals SD rats fed 6 inds of Baechu-kimchi containing diet during 4 weeks. Three kinds of freeze dried kimchi differ in fermentation period (not fermented, 3-, 6-week-fermented at 4$^{\circ}C$) were added at 5%, 10% of the diet containing 15% lard. The levels of serum total lipid and triglyceride and the content of liver total lipid and triglyceride of all kimchi groups were lower than those of a control group. But the levels of serum and liver cholesterol is not affected by kimchi intake. The triglyceride concentration of epididymal fat pad and feces of kimchi groups were higher than those of a control group. The food efficiency ratio, epididymal fat pad weight of 3-, 6-week-fermented kimchi 10% groups were significantly lower than control and not-fermented kimchi groups. Especially 6-week-fermented kimchi groups showed adipocytes, less in number and larger in size than those of other groups. The blastogenesis of spleen lymphocytes to LPS was higher in rats fed fermented kimchi diets than rats fed control and not-fermented kimchi diet. These results suggest that kimchi stimulates lipid mobilization to epididymal fat pad and lipid excretion via feces, so lower serum and liver triglyceride concentration. The fermented kimchi stimulate the proliferation of B cell and lower the lipid accumulation in epididymal fat pad, especially kimchi fermented for 6 weeks at 4$^{\circ}C$ lower the adipose cell number.

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In vitro Stimulation of NK Cells and Lymphocytes Using an Extract Prepared from Mycelial Culture of Ophiocordyceps sinensis

  • Sun-Hee Jang;Jisang Park;Seung-Hwan Jang;Soo-Wan Chae;Su-Jin Jung;Byung-Ok So;Ki-Chan Ha;Hong-Sig Sin;Yong-Suk Jang
    • IMMUNE NETWORK
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    • 제16권2호
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    • pp.140-145
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    • 2016
  • Ophiocordyceps sinensis is a natural fungus that has been valued as a health food and used in traditional Chinese medicine for centuries. The fungus is parasitic and colonizes insect larva. Naturally occurring O. sinensis thrives at high altitude in cold and grassy alpine meadows on the Himalayan mountain ranges. Wild Ophiocordyceps is becoming increasingly rare in its natural habitat, and its price limits its use in clinical practice. Therefore, the development of a standardized alternative is a great focus of research to allow the use of Ophiocordyceps as a medicine. To develop an alternative for wild Ophiocordyceps, a refined standardized extract, CBG-CS-2, was produced by artificial fermentation and extraction of the mycelial strain Paecilomyces hepiali CBG-CS-1, which originated from wild O. sinensis. In this study, we analyzed the in vitro immune-modulating effect of CBG-CS-2 on natural killer cells and B and T lymphocytes. CBG-CS-2 stimulated splenocyte proliferation and enhanced Th1-type cytokine expression in the mouse splenocytes. Importantly, in vitro CBG-CS-2 treatment enhanced the killing activity of the NK-92MI natural killer cell line. These results indicate that the mycelial culture extract prepared from Ophiocordyceps exhibits immune-modulating activity, as was observed in vivo and this suggests its possible use in the treatment of diseases caused by abnormal immune function.

Effects of Olaquindox and Cyadox on Immunity of Piglets Orally Inoculated with Escherichia coli

  • Ding, Mingxing;Yuan, Zonghui;Wang, Yulian;Zhu, Huiling;Fan, Shengxian
    • Asian-Australasian Journal of Animal Sciences
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    • 제18권9호
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    • pp.1320-1325
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    • 2005
  • A 2${\times}$3 factorial arrangement of treatments was used to determine the effects of olaquindox and cyadox on immune response of Landrace${\times}$Large-White geld piglets that had been orally given 10$^{10}$ CFU of Escherichia coli (E. coli, O$_{139}$:K$_{88}$). Factors included (1) E. coli inoculation or control, and (2) no antimicrobials, 100 mg/kg olaquindox and 100 mg/kg cyadox in the basal diet respectively. E. coli inoculums were orally administered 7 days after the diets were supplemented with olaquindox and cyadox. The effects of the two antimicrobials were assessed in terms of: (1) average daily gain (ADG), (2) systemic immune response (the number of white blood cells and lymphocytes, leukocyte bactericidal capacity, lymphocyte proliferation response to PHA, immunoglobulin concentrations, and total serous hemolytic complement activity), and (3) intestinal mucosal immunity including the number of intraepithelial lymphocytes (IELs) and immunoglobulin A secreting cells (ASCs) in the intestinal lamina propria. E. coli inoculation reduced ADG (p<0.05) during the period of d 0 to d 14 after the challenge while the antimicrobial supplementations improved ADG (p<0.01) during the experiment. ADG in cyadox-supplemented pigs was higher (p<0.05) than that in olaquindox-supplemented pigs. The antimicrobials decreased IEL and ASC counts in the jejunum and ileum (p<0.01) while E. coli inoculation caused them to increase (p<0.01). Jejunal ASCs in the cyadox-supplemented pigs were lower (p<0.05) than those in the olaquindox-supplemented. E. coli elicited increase (p<0.05) in white blood cell counts, leukocyte bactericidal capacity, lymphocyte proliferation rate, serous IgA concentrations, and serous hemolytic complement activity. The antimicrobials decreased the measured systemic immune parameters, but not significantly (p>0.05). The data suggest that olaquindox and cyadox suppress E. coli-induced immune activation, especially intestinal mucosal immune activation, which may be involved in the observed growth promotion.

면역증강물질 강화 청국장 발효 (The Bacterial Biological Response Modifier Enriched Chungkookjang Fermentation)

  • 홍성욱;김주영;이봉기;정건섭
    • 한국식품과학회지
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    • 제38권4호
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    • pp.548-553
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    • 2006
  • 전통된장에서 B 세포만을 선택적으로 증가시키는 면역증강 물질을 생산하는 B. licheniformis E1을 분리한 바 있다(22). 이를 이용하여 면역증강 청국장을 제조하였으나 관능적인 측면에서 기호도가 좋지 않았고 아미노태 질소함량이 식품공전의 규격(280 mg%)에 적합하지 않았다. 이를 보완하기 위해 시판 청국장으로부터 발효미생물을 분리하였다. 단백질 분해효소 활성과 청국장 발효제조시 기호도에서도 가장 우수한 청국장 발효미생물이 선발되었고 동정한 결과 B. subtilis S2로 명명하였다. 청국장 발효에 있어서 최적 발효온도와 최적 발효시간을 조사한 결과 $40^{\circ}C$에서 48시간 동안 발효하였을 때의 기호도가 가장 우수하였다. 단일균주 B. licheniformis E1, B. subtilis S2 및 B. licheniformis E1과 B. subtilis S2의 혼합균주를 각각 접종하여 발효제조한 청국장과 시판 청국장을 대조구로 사용하여 청국장의 기호도, 이화학적 특성조사와 면역증강 활성 비교를 조사하였는데, B. licheniformis E1과 B. subtilis S2의 혼합균주를 접종하여 제조한 청국장에서 기호도가 가장 우수하였고 아미노태 질소함량과 조단백질 함량은 359 mg%와 45.6%로 식품공전의 규격에 적합하였다. 청국장으로부터 면역증강 물질을 분리하여 마우스 비장 림프구의 증식 및 억제 현상을 측정한 결과, 20,480 unit으로 림프구의 증식에 있어서도 가장 효과적인 것으로 확인되었다.

Immunomodulating activities of water extract from xanthium strumarium 2

  • Moon, Eun-Yi;Park, Seung-Yong;Ahn, Mee-Ja;Ahn, Jong-Woong;Zee, Ok-Pyo;Park, Eun-kyue
    • Archives of Pharmacal Research
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    • 제14권3호
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    • pp.217-224
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    • 1991
  • One of water and/or methanol extracts from 14 herbal deugs which were screened using murine splenocytes showed immunosuppressive activities previously. After water extract from Xanthium strumarium was treated with chloroform. $100 \mu{g/ml}$ of water layer (XS-WCI) has very strong immunosimulating activities tested by $^3H$-thmidine incorporation (control as $100 \mu{g/ml}$, 26345 cpm was 69515 cpm). MLR also appears to be simulated strongly (control vs $100 \mu{g/ml}$, 4962 cpm vs 78688 cpm). When $100 \mu{g/ml}$ of XS-WCI and $0.8 \mu{g/ml}$ of concanavalin a (ConA) were added. more $^3H$-thymidine were incorporated significantly, compared with $0.8 \mu{g/ml}$ of ConA only. In contrast with ConA. results from $5 \mu{/ml}$ of lipopolysaccharide (LPS) and $100 \mu{g/ml}$ of XS-WCI were not different. compared with $5\mu{/ml}$of LPS only. These results indicated the responses of XS-WCI to B cell and T cell may be different. XS-WCI was injected intraperitoneally (10 mg/kg. 50mg/kg/ 100 mg/kg) for 4 days or 10 days and tested secretion of IgM or IgG by direct and indirect hemolytic plaque-forming cell assays, respectively. Numbers of hemolytic plaques for both IgM and IgG were increased significantly. Especially, secretion of IgGs was increased more than 10 times. After administration of XS-WCI for 7 days (50 mg/kg. 100 mg/kg) splenomegaly deu to graft vs host reaction was observed. Human lymhocytes separated from whole blood by Ficoll-Hypaque method were also proliferated after treatment of $10 \mu{g/ml}$ and $50 \mu{g/ml}$ of XS-WCI. As seen in murine lymphocytes, human lymphocyte proliferation was increased synergistically after treatment with both of XS-WCI and phytohemagglutinin (PHA). It appears that XS-WCI may have potential immunosimulating activities and that it remains to be purified further for isolation of active components.

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가토 피부상처에서의 개방드레싱과 밀봉드레싱의 효과에 대한 형태학적 비교 (Morphological Comparision of the Effect of Open and Occlusive Dressing on Rabbit Skin Wound)

  • 강영희;홍해숙
    • Journal of Korean Biological Nursing Science
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    • 제5권1호
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    • pp.23-33
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    • 2003
  • 본 연구는 체중 3.0kg의 가토 수컷 10마리를 이용하여 피부의 외상을 입힌 후 개방드레싱과 밀봉드레싱이 상처의 치유과정에서의 효과와 형태학적 차이를 비교하기 위해 1cm의 절개창과 $1.0{\times}0.2cm$의 피부절제창을 만든 후 개방드레싱군은 1일 2회 betadine으로 소독한 후 상처부위를 노출시켜 5, 10 및 15일째에 관찰하였으며, 밀봉드레싱군은 매일 betadine으로 소독하고 1% silver sulfadiazine 크림을 도포한 후 거즈를 덮어 5, 10 및 15일째에 광학현미경으로 관찰하여 다음과 같은 결론을 얻었다. 피부를 절개한 군과 절제한 군을 개방드레싱 및 밀봉드레싱을 각각 시행한 5일 후에는 딱지가 형성되었고 표피의 재생은 상처의 가장자리에서부터 시작하였다. 진피의 표층에는 호중구, 단구 및 림프구의 침윤이 일어났고 부종과 섬유아세포의 증식이 경하게 일어났다. 수상 후 개방드레싱 및 밀봉드레싱을 시행한 10일 후에는 딱지는 탈락되었고 표피는 재생되어 연속적이었다. 모세혈관의 수와 염증세포의 침윤은 감소하였다. 부종과 섬유아세포의 증식은 더욱 증가하였다. 수상 후 개방 및 밀봉드레싱을 시행한 후 15일에는 표피의 재생은 완성되어 각질이 형성되었다. 진피에는 염증세포의 침윤, 부종 및 혈관의 증식은 소실되었고 섬유아세포 및 교원섬유의 양은 증가하였다. 피부를 절개한 군은 절제 군에 비해 반흔의 양은 적었고 드레싱방법에따른 치유과정의 차이는 없었다. 이상의 성적으로 보아 상처의 치료는 드레싱의 방법보다 상처의 소독이 중요한 역할을 하는 것으로 사료된다.

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카드뮴투여가 Balb/c 마우스의 면역반응에 미치는 영향 (Effect of Cadmium Chloride on the Immune Responses in Balb/c Mouse)

  • 염정호;강현철;고대하
    • 한국환경보건학회지
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    • 제21권3호
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    • pp.16-22
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    • 1995
  • This study was designed to investigate the antibody production to sheep red blood cells(SRBC) and proliferation of mitogen-stimulated spleen cells in Balb/c mice which received cadmium chloride. The mice were divided into three independent groups which were one control and two experimental groups by the cadmium treatment or not. No specific treatment was done for the control group. One of two experimental groups, which is called 'pre-treatment group' in this paper, was subcutaneously injected with low dose of cadmium chloride(0.5 mg/kg/day) for 5 consecutive days before the primary SRBC immunization. The other called 'non-pretreatment group' was only pretreated with normal saline. Both experimental groups were intraperitoneally injected with high dose of cadmium chloride(5 mg/kg) 8 hours before the primary immunization. Mice were intraperitoneally immunized twice with 2% SRBC suspension containing $10^8$ cells. The results obtained were as follows, 1. The PFG responses to SRBC were significantly increased in two experimental groups, cadmium pretreatment and non-pretreatment compared with that of control group(p<0.05). 2. The total antibody titers to SRBC in cadmium treated groups were similar to that of control group, but titers of IgG antibody were significantly elevated(p<0.01). 3. The proliferation response of spleen lymphocytes to various mitogens was suppressed in proportion to the concentration of cadmium and the degree of cadmium accumulation in liver was increased in the cadmium treated groups. These results suggest that cadmium chloride could affect on mouse immune response, especially its cell mediated immune response could be decreased while its humoral immune response could be increased, which may not be influenced by the administration methods or pretreatment of cadmium to mouse.

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CD30-Mediated Regulation of Cell Adhesion Molecule Expression on Murine T Cells

  • Nam, Sang-Yun
    • IMMUNE NETWORK
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    • 제3권1호
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    • pp.8-15
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    • 2003
  • Background: CD30 is a member of TNF receptor family and expressed on lymphocytes and other hematopoietic cells following activation as well as Hodgkin and Reed-Sternberg cells in Hodgkin's lymphoma. In this study, CD30-mediated regulation of cell adhesion molecule expression on normal activated mouse T cells was investigated. Methods: Mouse T cells were activated with anti-CD3 antibody for induction of CD30, which was cross-linked by immobilized anti-CD30 antibody. Results: High level of CD30 expression on T cells was observed on day 5, but only little on day 3 even under culture condition resulting in an identical T cell proliferation, indicating that CD30 expression requires a prolonged stimulation up to 5 days. Cross-linking of CD30 alone altered neither proliferation nor apoptosis of normal activated T cells. Instead, CD30 appeared to promote cell adherence to culture substrate, and considerably upregulated ICAM-1 and, to a lesser extent, ICAM-2 expression on activated T cells, whereas CD2 and CD18 (LFA-1) expression was not affected. None of cytokines known as main regulators of ICAM-1 expression on tissue cells (IL 4, $IFN{\gamma}$ and $IFN{\alpha}$) enhanced ICAM-1 expression in the absence of CD30 signals. On the other hand, addition of $NF-{\kappa}B$ inhibitor, PDTC (0.1 mM) completely abrogated the CD30-mediated upregulation of ICAM-1 expression, but not CD2 and ICAM-2 expression. Conclusion: This results support that CD30 upregulates ICAM-1 expression of T cell and such regulation is not mediated by higher cytokine production but $NF-{\kappa}B$ activation. Therefore, CD30 may play important roles in T-T or T-B cell interaction through regulation of ICAM-1, and -2 expression.

브로콜리로부터 분리한 추출물의 In vitro 면역증진 활성평가 및 화학적 특성 (Chemical Properties and Assessment of Immunomodulatory Activities of Extracts isolated from Broccoli)

  • 곽봉신;박혜령;이수정;최혁준;신광순
    • 한국식품영양학회지
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    • 제30권6호
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    • pp.1140-1148
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    • 2017
  • For the purpose of developing new immunomodulatory agents from broccoli, ethanol extract (BCEE), hot water extract (BCHW), and crude polysaccharide (BCCP) were isolated from broccoli, and their immunomodulatory activities and chemical properties were examined. In the in vitro cytotoxicity analysis, BCHW and BCCP did not affect the growth of tumor cells and normal cells. Murine peritoneal macrophages stimulated with BCCP showed higher production of IL-6, IL-12, and $TNF-{\alpha}$ cytokines than those stimulated with BCHW. Also, BCHW and BCCP did not show proliferation of splenic lymphocytes. In the in vitro assay for intestinal immunomodulatory activities, only BCCP enhanced GM-CSF secretion and the bone marrow cell-proliferating activity via cells in Peyer's patches at $1,000{\mu}g/mL$. Also, BCHW mainly contained 33.7% neutral sugars, such as arabinose, glucose, and galactose, and 30.7% uronic acid, and BCCP consisted of 42.6% neutral sugars, including arabinose, galactose, and glucose, and 50.5% uronic acid. The above results lead us to conclude that crude polysaccharide (BCCP) isolated from broccoli causes considerably high cytokine production in peritoneal macrophages and bone marrow cell proliferation, and the polysaccharide extraction process is indispensable for separation of new immunomodulatory agents from broccoli.