Journal of Clinical Physiology
Online ISSN : 2435-1695
Print ISSN : 0286-7052
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Journal of Clinical Physiology
Displaying 1-5 of 5 articles from this issue
Review Article
Original Article
  • Ryoma MICHISHITA, Shotaro KAWAKAMI, Miho ANZAI, Kodai TAKAHASHI, Emika ...
    2025 Volume 55 Issue 1 Pages 15-21
    Published: February 01, 2025
    Released on J-STAGE: April 12, 2025
    JOURNAL OPEN ACCESS

     Background: This study investigated the acute effects of heat-not-burn cigarettes and combustion cigarettes on vascular endothelial function.

     Methods: Eight healthy young males with a smoking habit were included in this study. Each participant used either new-generation heat-not-burn or traditional tobacco combustion cigarettes, and vascular endothelial function was measured before and 120 min after using either type of cigarette.

     Results: In both conditions, the reactive hyperemia index was significantly lower at 90 and 120 min after smoking than before smoking (p < 0.05); however, no significant difference was observed between the two conditions at any point.

     Conclusion: These results indicate that heat-not-burn and combustion cigarettes have similar acute effects on vascular endothelial function.

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  • Yoshimasa OGATA, Miki MORI, Keisuke AITA, Satoshi YOSHIOKA, Risa SHIRA ...
    2025 Volume 55 Issue 1 Pages 23-28
    Published: February 01, 2025
    Released on J-STAGE: April 12, 2025
    JOURNAL OPEN ACCESS

     Background: Basophils circulating in the blood play a proinflammatory role at sites of allergic inflammation in two stages: tissue accumulation and activation. This study analyzed the activation-enhancing effects of chemokines on chemokine-pretreated basophils using a two-step stimulation model.

     Methods: Basophils were obtained from volunteers with no history of allergic disease. Cells were pretreated with chemokines for 30 minutes and then activated for 45 minutes with IgE-mediated stimulus plus chemokines. The percent histamine release of basophils was measured.

     Results: The activation-enhancing effect of MCP-1 in the presence of basophils (24.3%±6.3%) was significantly decreased (6.8%±4.1%) when the cells were pretreated with MCP-1 (p < 0.01). On the other hand, the enhancing effect of eotaxin (9.5%±8.0%) was maintained (8.8%±3.8%) when the cells were pretreated with eotaxin (p > 0.05).

     Conclusion: The results indicate that basophils retain their histamine release-enhancing effect when eotaxin is used at both the pretreatment and activation steps. However, the activation enhancing effect of MCP-1 was reduced when basophils were pretreated with MCP-1. Our two-step model of human basophil pretreatment and activation showed different patterns of chemokine action.

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  • Kazunori YANAGISAKO, Kazuhiko HANASHIRO, Koji TAKABATAKE, Yuto MIYAZAT ...
    2025 Volume 55 Issue 1 Pages 29-38
    Published: February 01, 2025
    Released on J-STAGE: April 12, 2025
    JOURNAL OPEN ACCESS

     Background: E-selectin, a cell adhesion molecule, is involved in the early stage of atherosclerosis, and lipopolysaccharide (LPS) is involved in upregulating E-selectin expression. The effect of nobiletin, a polymethoxylated flavone derived from citrus fruits, on LPS-induced E-selectin expression remains unclear.

     Objectives: This study explored the inhibitory effects of nobiletin on LPS-induced E-selectin expression in human umbilical vascular endothelial cells (HUVECs) and the involvement of reactive oxygen species (ROS) in the inhibitory mechanism.

     Methods: HUVECs were exposed to LPS (0−50 ng/ml) after pretreatment with nobiletin (0−200 μM), and E-selectin mRNA expression was quantified by real-time polymerase chain reaction in a concentration- and time-dependent manner. Differences in LPS-induced E-selectin mRNA expression between pretreatment and nontreatment with nobiletin were statistically analyzed. The production of superoxide, which is a precursor of most ROS, was quantified using the tetrazolium salt (WST-1) assay, and intracellular ROS production was detected using the highly sensitive DCFH-DA dye under a fluorescence microscope.

     Results: The LPS and nobiletin exposure exerted no significant effect on cell viability in the concentration range used. E-selectin mRNA expression increased in a concentration-dependent manner when HUVECs were exposed to LPS (0−50 ng/ml) for 3 h (10 ng/ml, p < 0.05; 25 and 50 ng/ml, p < 0.01). After LPS stimulation (10 ng/ml), E-selectin mRNA expression significantly increased in a time-dependent manner and reached the maximum at 12 h (3, 6, 12, and 24 h, p < 0.01). Pretreatment of HUVECs with nobiletin downregulated the LPS-induced E-selectin mRNA expression in a concentration-dependent manner (50, 100, and 200 μM, p<0.01). Apocynin, an NADPH oxidase inhibitor, downregulated the LPS-induced E-selectin mRNA expression in a concentration-dependent manner (100μM, p < 0.01). Moreover, nobiletin (200μM) exerted significant inhibitory effects on LPS-induced ROS production in both the WST-1 assay (p < 0.01) and cell images.

     Conclusion: Nobiletin downregulated LPS-induced E-selectin mRNA expression through inhibition of LPS-induced superoxide production.

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