Sexual Dimorphism of Spinal Neural Circuits Controlling the Mouse External Urethral Sphincter With and Without Spinal Cord Injury

Author:

Karnup Sergei1ORCID,Hashimoto Mamoru2,Cho Kang Jun2,Beckel Jonathan1ORCID,de Groat William1,Yoshimura Naoki12ORCID

Affiliation:

1. Department of Pharmacology and Chemical Biology University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA

2. Department of Urology University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA

Abstract

ABSTRACTSpinal cord injury (SCI) disrupts coordination between the bladder and the external urinary sphincter (EUS), leading to transient or permanent voiding impairment, which is more severe in males. Male versus female differences in spinal circuits related to the EUS as well as post‐SCI rewiring are essential for understanding of sex‐/gender‐specific impairments and possible recovery mechanisms. To quantitatively assess differences between EUS circuits in males versus females and in spinal intact (SI) versus SCI animals, we retrogradely traced and counted EUS‐related neurons. In transgenic ChAT‐GFP mice, motoneurons (MNs), interneurons (INs), and propriospinal neurons (PPNs) were retrogradely trans‐synaptically traced with PRV614‐red fluorescent protein (RFP) injected into EUS. EUS‐MNs in dorsolateral nucleus (DLN) were separated from other GFP+ MNs by tracing them with FluoroGold (FG). We found two morphologically distinct cell types in DLN: FG+ spindle‐shaped bipolar (SB‐MNs) and FG rounded multipolar (RM‐MNs) cholinergic cells. Number of MNs of both types in males was twice as large as in females. SCI caused a partial loss of MNs in all spinal nuclei. After SCI, males showed a fourfold rise in the number of RFP‐labeled cells in retro‐DLN (RDLN) innervating hind limbs. This suggests (a) an existence of direct synaptic interactions between spinal nuclei and (b) a post‐SCI increase of non‐specific inputs to EUS‐MNs from other motor nuclei. Number of INs and PPNs deferred between males and females: In SI males, the numbers of INs and PPNs were ∼10 times larger than in SI females. SCI caused a twofold decrease of INs and PPNs in males but not in females.

Funder

National Institutes of Health

Publisher

Wiley

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