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A Fragrant Environment Containing α-Pinene Suppresses Tumor Growth in Mice by Modulating the Hypothalamus/Sympathetic Nerve/Leptin Axis and Immune System. | LitMetric

AI Article Synopsis

  • The study explores how a fragrant environment (FE) containing α-pinene affects tumor growth in melanoma mice, revealing a ~40% reduction in tumor size.
  • Exposure to the FE led to decreased leptin levels and increased sympathetic nervous activity, while certain immune cells (B cells, CD4 T cells, CD8 T cells, and natural killer cells) were found to be more abundant.
  • These findings suggest that the FE may enhance immune response and activate key neurohormonal pathways, potentially offering a mechanism for how environmental factors can influence cancer outcomes.

Article Abstract

The environment is thought to affect outcomes in patients with cancer; however, this relationship has not been proven directly. Recently, an enriched environment, as a model of a positive environment, has been shown to suppress tumor growth by lowering leptin production through a pathway involving the hypothalamus/sympathetic nerve/leptin axis. We previously reported that a fragrant environment (FE) containing α-pinene suppressed tumor growth in mice; however, the underlying mechanism has not been elucidated. Accordingly, in this study, we investigated changes in the neuroendocrine and immune systems following exposure to an FE. Mice were exposed to α-pinene (5 h/day) for 4 weeks prior to tumor implantation with murine melanoma cells and 3 weeks after transplantation. In addition to the evaluation of tumor growth, the blood, spleen, and hypothalamus were collected 3 weeks after transplantation, and neuroendocrinological and immunological parameters were measured. Tumor size was ~40% smaller in mice exposed to FE. Moreover, plasma noradrenaline concentrations, which reflected sympathetic nervous activity, tended to increase, and leptin levels were significantly decreased in FE-exposed mice. Levels of stress hormones, such as plasma corticosterone and adrenaline, did not change in the 2 groups. In the hypothalamus, brain-derived neurotrophic factor protein levels and glucose-1-phosphate concentrations were decreased in the FE group. Additionally, numbers of B cells, CD4 T cells, CD8 T cells, and natural killer cells increased in the FE-exposed mice. These neurohormonal and immunological changes in the FE-exposed mice suggested that the FE may activate the hypothalamus/sympathetic nerve/leptin axis and immune system, thereby retarding tumor growth.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6484235PMC
http://dx.doi.org/10.1177/1534735419845139DOI Listing

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