1.Antitumor effects of the polysaccharides from Gloiopeltis furcata on H_(22) tumor bearing mice
Jie YU ; Meizhen CHEN ; Zhaocheng XU ; Shichao CUI ; Wu TANG
Chinese Journal of Marine Drugs 2001;0(05):-
Objective To study the antitumor effect and the mechanism of the polysaccharide from Gloipeltis furcata on H_(22),tumor bearing mice.Methods The polysaccharides from Gloipeltis furcata were administered by oral route in mice bearing H_(22) tumor.The treatments lasted for 7 days.The inhibition rate against H_(22) tumor and the indices of thymus, spleen and liver were measured.In addition,the levels of antibodies against H_(22) tumor and GPT in serum,and GPT,GOT,MDA and SOD in liver were measured using commercially available kits.Results The administration of the polysaccharides from Gloipeltis furcata(200 mg?kg~(-1)?d~(-1) and 400 mg?kg~(-1)?d~(-1) ) for 7 days,the inhibition rates of H_(22) tumor were 35.64%(P
2.Design and preliminary application of outdoor flying pigeon-robot.
Hao WANG ; Shaokang WANG ; Zhaocheng QIU ; Qi ZHANG ; Shuai XU
Journal of Biomedical Engineering 2022;39(6):1209-1217
Control at beyond-visual ranges is of great significance to animal-robots with wide range motion capability. For pigeon-robots, such control can be done by the way of onboard preprogram, but not constitute a closed-loop yet. This study designed a new control system for pigeon-robots, which integrated the function of trajectory monitoring to that of brain stimulation. It achieved the closed-loop control in turning or circling by estimating pigeons' flight state instantaneously and the corresponding logical regulation. The stimulation targets located at the formation reticularis medialis mesencephali (FRM) in the left and right brain, for the purposes of left- and right-turn control, respectively. The stimulus was characterized by the waveform mimicking the nerve cell membrane potential, and was activated intermittently. The wearable control unit weighted 11.8 g totally. The results showed a 90% success rate by the closed-loop control in pigeon-robots. It was convenient to obtain the wing shape during flight maneuver, by equipping a pigeon-robot with a vivo camera. It was also feasible to regulate the evolution of pigeon flocks by the pigeon-robots at different hierarchical level. All of these lay the groundwork for the application of pigeon-robots in scientific researches.
Animals
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Columbidae/physiology*
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Robotics/methods*
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Cerebral Cortex
3.Development of a flow cytometry method for detection of bovine multi-cytokines.
Zhaocheng ZHU ; Aihong XIA ; Zhaoli CAO ; Xin LI ; Xiang CHEN ; Zhengzhong XU ; Xin An JIAO
Chinese Journal of Biotechnology 2023;39(1):347-358
This study aims to develop a method to detect bovine multi-cytokines based on flow cytometry. Previously we have prepared and screened monoclonal antibodies against bovine cytokines IFN-γ, IL-2, TNF-α, IP-10 and MCP-1. These bovine cytokine monoclonal antibodies were fluorescently labeled, and the combination of antibody and cell surface molecules were used to develop the method for detecting bovine multi-cytokines. Subsequently, the developed method was used to determine the cytokine expression profile of Mycobacterium bovis BCG infected bovine peripheral blood mononuclear cells in vitro, and evaluate the cytokine expression level of peripheral blood CD4+ T cells of tuberculosis-positive cattle. The bovine multi-cytokine flow cytometry detection method can effectively determine the cytokine expression of BCG-infected bovine peripheral blood T lymphocytes. Among them, the expression levels of IFN-γ, IL-2, and TNF-α continue to increase after 40 hours of infection, while the expression levels of IP-10 and MCP-1 decreased. The combined detection of IFN-γ, IL-2, and TNF-α on CD4+ T lymphocytes in peripheral blood of cattle can effectively distinguish tuberculosis-positive and tuberculosis-negative samples. This method may facilitate evaluating the level of cellular immune response after bovine pathogen infection and vaccine injection.
Cattle
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Animals
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Cytokines
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BCG Vaccine/metabolism*
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Tumor Necrosis Factor-alpha/metabolism*
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Interleukin-2
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Flow Cytometry/methods*
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Chemokine CXCL10/metabolism*
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Leukocytes, Mononuclear
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CD4-Positive T-Lymphocytes/metabolism*
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Tuberculosis
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Antibodies, Monoclonal/metabolism*