Poster, Podium & Video Sessions
Presentation Authors: Tsuyoshi Majima*, Yasuhito Funahashi, Nagoya, Japan, Naoki Kawamorita, Sendai, Japan, Yoshihisa Matsukawa, Tokunori Yamamoto, Nagoya, Japan, Naoki Yoshimura, PIttsburgh, PA, Momokazu Gotoh, Nagoya, Japan
Introduction: We investigated whether spinal cord microglia are involved in colon-to-bladder neural crosstalk in a rat model of colitis.
Methods: Adult female SD rats were divided into A) control, B) colitis, and C) colitis + minocycline groups. Experimental colitis was induced by instilling 50% trinitrobenzene sulfonic acid into the distal colon in groups B and C; vehicle was administered in group A. Minocycline (200 mg/day), a microglial inhibitor, was continuously infused into the intrathecal space in group C; groups A and B were given the vehicle. On day 7:
(1) an awake cystometrogram (CMG) was performed;
(2) nociceptive licking and freezing behavior induced by intravesical instillation of resiniferatoxin was observed;
(3) the distal colon was stained with hematoxylin-eosin (HE);
(4) immunofluorescence staining for CD 11b, a microglial marker, was performed on the L6 spinal cord;
(5) reverse transcription polymerase chain reaction for mRNA was performed on the L6 spinal cord;
(6) the bladder was stained with toluidine blue.
Results: (1) CMG in group B showed significantly (p < 0.01) shorter intercontraction intervals (ICI) than in group A. Group C showed significantly (p < 0.01) longer ICI than group B.
(2) There were no significant differences in licking events among the 3 groups. However, the number of freezing events was significantly (p < 0.01) greater in group B than in group A. Group C showed significantly (p < 0.05) fewer freezing events than group B.
(3) HE staining showed substantial inflammation in the distal colon in groups B and C compared with that in group A.
(4) The number of CD 11b-positive cells significantly differed among groups in the following order: group B > group C > group A.
(5) The mRNA expressions of interleukin-1β, chemokine ligand 3, and brain-derived neurotrophic factor in the L6 spinal cord were significantly (p<0.05) increased in group B compared with those in group A. However, group C showed significantly (p<0.05) less mRNA expression of these molecules than group B.
(6) Toluidine blue staining in group B showed significantly (p<0.01) more total and degranulated mast cells in the bladder than group A. Group C showed significantly (p<0.05) fewer total and degranulated mast cells in the bladder than group B.
Conclusions: Spinal microglia probably play an important role in colitis-induced bladder overactivity and enhanced bladder pain sensitivity in colitic rats.
Source Of Funding: DOD W81XWH-12-1-0565; NIH DK088836
Saturday, May 13
9:30 AM – 11:30 AM
Sunday, May 14
7:00 AM – 9:00 AM
Sunday, May 14
9:50 AM – 10:00 AM