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Injection of L actobacillus casei strain S hirota affects autonomic nerve activities in a tissue‐specific manner, and regulates glucose and lipid metabolism in rats
Author(s) -
Tanida Mamoru,
Imanishi Kazuki,
Akashi Haruna,
Kurata Yasutaka,
Chonan Osamu,
Naito Eiichiro,
Kunihiro Satoru,
Kawai Mitsuhisa,
Katokataoka Akito,
Shibamoto Toshishige
Publication year - 2014
Publication title -
journal of diabetes investigation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.089
H-Index - 50
eISSN - 2040-1124
pISSN - 2040-1116
DOI - 10.1111/jdi.12141
Subject(s) - endocrinology , medicine , vagus nerve , autonomic nerve , autonomic nervous system , sympathetic nervous system , adipose tissue , efferent nerve , efferent , blood pressure , parasympathetic nervous system , heart rate , afferent , stimulation
Aims/Introduction Previously, it was observed that long‐term ingestion of a probiotic strain L actobacillus casei S hirota ( LcS ) ameliorates insulin resistance and glucose intolerance in rats fed a high‐fat diet. In the present study, we examined its possible role in the autonomic nervous system during LcS ‐induced modulations in glucose and lipid metabolism or cardiovascular functions. Materials and Methods The present study examined the effects of intragastric ( IG ) LcS injection on autonomic nerve tones in anesthetized rats by electrophysiological method. Results We found that an IG injection of LcS suppressed neural activity of sympathetic nerves supplying the white adipose tissue of urethane‐anesthetized rats in a dose‐dependent manner, whereas sympathetic nerve outflow to brown adipose tissue was not affected by the IG LcS injection. Furthermore, the IG LcS injection reduced efferent sympathetic nerve outflow to the adrenal gland and liver, but did not alter gastric vagal nerve activity, renal sympathetic nerve activity, as well as mean arterial pressure. To test the involvement of afferent vagal nerves and the abdominal organs, we examined the adrenal sympathetic response to an LcS injection in rats with ablated afferent vagal nerves, and found that the adrenal sympathetic nerve response to LcS was inhibited in vagotomized rats. In addition, we found that oral ingestion of LcS attenuated the hyperglycemic response to glucose loading and blood glycerol levels in conscious rats. Conclusions Our data suggest that LcS might affect tissue‐specific autonomic nerves through the afferent vagal nerve pathway to modulate glucose and lipid metabolism.

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