4.6 Article

l-Theanine Protects Bladder Function by Suppressing Chronic Sympathetic Hyperactivity in Spontaneously Hypertensive Rat

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METABOLITES
卷 11, 期 11, 页码 -

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MDPI
DOI: 10.3390/metabo11110778

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L-theanine; chronic sympathetic hyperactivity; bladder dysfunction; prevention; oral administration

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This study evaluated the effects of orally administered l-theanine in spontaneously hypertensive rats with bladder dysfunction induced by chronic sympathetic hyperactivity. The results showed that l-theanine significantly decreased sympathetic nervous system activity, increased bladder capacity, and improved bladder contractility, suggesting its potential in preventing bladder dysfunction caused by chronic sympathetic hyperactivity.
Chronic sympathetic hyperactivity is known to affect metabolism and cause various organ damage including bladder dysfunction. In this study, we evaluated whether l-theanine, a major amino acid found in green tea, ameliorates bladder dysfunction induced by chronic sympathetic hyperactivity as a dietary component for daily consumption. Spontaneously hypertensive rats (SHRs), as an animal model of bladder dysfunction, were divided into SHR-water and SHR-theanine groups. After 6 weeks of oral administration, the sympathetic nervous system, bladder function, and oxidative stress of bladder tissue were evaluated. The mean blood pressure, serum noradrenaline level, and media-to-lumen ratio of small arteries in the suburothelium were significantly lower in the SHR-theanine than in the SHR-water group. Micturition interval was significantly longer, and bladder capacity was significantly higher in the SHR-theanine than in the SHR-water group. Bladder strip contractility was also higher in the SHR-theanine than in the SHR-water group. Western blotting of bladder showed that expression of malondialdehyde was significantly lower in the SHR-theanine than in the SHR-water group. These results suggested that orally administered l-theanine may contribute at least partly to the prevention of bladder dysfunctions by inhibiting chronic sympathetic hyperactivity and protecting bladder contractility.

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