TY - JOUR
T1 - Spinal Transection Switches the Effect of Metabotropic Glutamate Receptor Subtype 7 from the Facilitation to Inhibition of Ejaculation
AU - Masugi-Tokita, Miwako
AU - Kubota, Shigehisa
AU - Kobayashi, Kenichi
AU - Yoshida, Tetsuya
AU - Kageyama, Susumu
AU - Sakamoto, Hirotaka
AU - Kawauchi, Akihiro
N1 - Funding Information:
We especially thank Dr. Herman van der Putten from the Novartis Institutes for BioMedical Research (Basel, Switzerland) for providing the mGluR7 KO mice, Dr. Pierre A. Guertin for technical advice and Dr. Ryoichiro Kageyama for providing an excellent research environment. This work was supported by Japan Society for the Promotion of Science KAKENHI (Grant Numbers 20500313 and 23500415 to MMT). The authors declare that there are no conflicts of interest. All authors contributed to the study conception and design. Material preparation was performed by MMT and HS, data collection was performed by MMT, and KK, analysis was performed by MMT and SK. The first draft of the manuscript was written by MMT and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.
Funding Information:
This work was supported by Japan Society for the Promotion of Science KAKENHI (Grant Numbers 20500313 and 23500415 to MMT).
Publisher Copyright:
© 2022 IBRO
PY - 2023/1/15
Y1 - 2023/1/15
N2 - Metabotropic glutamate receptor subtype 7 (mGluR7) is a member of the group III mGluRs, which localize to presynaptic active zones of the central nervous system. We previously reported that mGluR7 knockout (KO) mice exhibit ejaculatory disorders, although they have normal sexual motivation. We hypothesized that mGluR7 regulates ejaculation by potentiating the excitability of the neural circuit in the lumbosacral spinal cord, because administration of the mGluR7-selective antagonist into that region inhibits drug-induced ejaculation. In the present study, to elucidate the mechanism of impaired ejaculation in mGluR7 KO mice, we eliminated the influence of the brain by spinal transection (spinalization). Unexpectedly, sexual responses of male mGluR7 KO mice were stronger than those of wild-type mice after spinalization. Histological examination indicated that mGluR7 controls sympathetic neurons as well as parasympathetic neurons. In view of the complexity of its synaptic regulation, mGluR7 might control ejaculation by multi-level and multi-modal mechanisms. Our study provides insight into the mechanism of ejaculation as well as a strategy for future therapies to treat ejaculatory disorders in humans.
AB - Metabotropic glutamate receptor subtype 7 (mGluR7) is a member of the group III mGluRs, which localize to presynaptic active zones of the central nervous system. We previously reported that mGluR7 knockout (KO) mice exhibit ejaculatory disorders, although they have normal sexual motivation. We hypothesized that mGluR7 regulates ejaculation by potentiating the excitability of the neural circuit in the lumbosacral spinal cord, because administration of the mGluR7-selective antagonist into that region inhibits drug-induced ejaculation. In the present study, to elucidate the mechanism of impaired ejaculation in mGluR7 KO mice, we eliminated the influence of the brain by spinal transection (spinalization). Unexpectedly, sexual responses of male mGluR7 KO mice were stronger than those of wild-type mice after spinalization. Histological examination indicated that mGluR7 controls sympathetic neurons as well as parasympathetic neurons. In view of the complexity of its synaptic regulation, mGluR7 might control ejaculation by multi-level and multi-modal mechanisms. Our study provides insight into the mechanism of ejaculation as well as a strategy for future therapies to treat ejaculatory disorders in humans.
KW - ejaculation
KW - glutamate
KW - lumbar spinothalamic (LSt) cells
KW - lumbosacral spinal cord
KW - mGluR7
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U2 - 10.1016/j.neuroscience.2022.11.012
DO - 10.1016/j.neuroscience.2022.11.012
M3 - Article
C2 - 36403690
AN - SCOPUS:85143545957
SN - 0306-4522
VL - 509
SP - 10
EP - 19
JO - Neuroscience
JF - Neuroscience
ER -