Microbial lysate upregulates host oxytocin
Date Issued
2017-03Publisher Version
10.1016/j.bbi.2016.11.002Author(s)
Varian, Bernard J.
Poutahidis, Theofilos
DiBenedictis, Brett T.
Levkovich, Tatiana
Ibrahim, Yassin
Didyk, Eliska
Shikhman, Lana
Cheung, Harry K.
Hardas, Alexandros
Ricciardi, Catherine E.
Kolandaivelu, Kumaran
Veenema, Alexa H.
Alm, Eric J.
Erdman, Susan E.
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Show full item recordPermanent Link
https://hdl.handle.net/2144/34299Version
Published version
Citation (published version)
Bernard J Varian, Theofilos Poutahidis, Brett T DiBenedictis, Tatiana Levkovich, Yassin Ibrahim, Eliska Didyk, Lana Shikhman, Harry K Cheung, Alexandros Hardas, Catherine E Ricciardi, Kumaran Kolandaivelu, Alexa H Veenema, Eric J Alm, Susan E Erdman. 2017. "Microbial lysate upregulates host oxytocin." Brain, Behavior, and Immunity, Volume 61, pp. 36 - 49. https://doi.org/10.1016/j.bbi.2016.11.002Abstract
Neuropeptide hormone oxytocin has roles in social bonding, energy metabolism, and wound healing contributing to good physical, mental and social health. It was previously shown that feeding of a human commensal microbe Lactobacillus reuteri (L. reuteri) is sufficient to up-regulate endogenous oxytocin levels and improve wound healing capacity in mice. Here we show that oral L. reuteri-induced skin wound repair benefits extend to human subjects. Further, dietary supplementation with a sterile lysate of this microbe alone is sufficient to boost systemic oxytocin levels and improve wound repair capacity. Oxytocin-producing cells were found to be increased in the caudal paraventricular nucleus [PVN] of the hypothalamus after feeding of a sterile lysed preparation of L. reuteri, coincident with lowered blood levels of stress hormone corticosterone and more rapid epidermal closure, in mouse models. We conclude that microbe viability is not essential for regulating host oxytocin levels. The results suggest that a peptide or metabolite produced by bacteria may modulate host oxytocin secretion for potential public or personalized health goals.
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