The circadian rhythm of bladder clock genes in the spontaneously hypersensitive rat.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2019
Historique:
received: 05 04 2019
accepted: 15 07 2019
entrez: 26 7 2019
pubmed: 26 7 2019
medline: 1 4 2020
Statut: epublish

Résumé

Circadian expression rhythms of clock gene products in the bladder are reportedly hindered by clock gene abnormalities. However, the role of clock gene products in various pathological lower urinary tract conditions is unknown. The present study examined the relationship between clock genes and voiding dysfunction in spontaneous hypertensive rats (SHR). The voluntary voiding behavior study using metabolic cages was performed in 18-weeks old male Wistar rats (control group, n = 36) and SHR (SHR group, n = 36) under 12-h light/12-h dark conditions. Bladders were harvested every 4 h at six time points (n = 6 for each time point for each group), and we analyzed the messenger RNA (mRNA) expression of several clock genes: period 2 (Per2), cryptochrome 2 (Cry2), brain and muscle aryl hydrocarbon receptor nuclear translocator-like protein 1 (Bmal1), circadian locomotor output cycles kaput (Clock), nuclear receptor subfamily 1, group D, member 1 (Rev-erbα), mechanosensors: transient receptor potential vanilloid channel 1 (TRPV1), TRPV4, Piezo1, and vesicular nucleotide transporter (VNUT) using real-time polymerase chain reaction. Though 24-h urination frequency for both light and dark periods was significantly higher in the SHR group, urine volume per voiding was significantly lower versus control. In controls, urine volume per voiding was significantly lower during the dark period (active phase) than the light period (rest phase); this parameter did not significantly differ between active and rest phases for SHR. SHR bladders showed significantly higher expression of Cry2 and Clock during the active phase compared to controls. In the SHR group, TRPV1, TRPV4, Piezo1, and VNUT mRNA levels were significantly higher during the active phase compared to the control group. We speculate that Cry2 and Clock may be contributing factors in the decrease of bladder capacity during the active phase in SHR through increase of TRPV1, TRPV4, Piezo1, and VNUT expression, but further research will be necessary to elucidate the precise mechanisms.

Identifiants

pubmed: 31344120
doi: 10.1371/journal.pone.0220381
pii: PONE-D-19-09749
pmc: PMC6658119
doi:

Substances chimiques

CLOCK Proteins EC 2.3.1.48

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0220381

Commentaires et corrections

Type : ErratumIn

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Yusuke Kimura (Y)

Division of Urology, Tottori University Faculty of Medicine, Yonago, Japan.
Division of Pathological Biochemistry, Tottori University Faculty of Medicine, Yonago, Japan.

Masashi Honda (M)

Division of Urology, Tottori University Faculty of Medicine, Yonago, Japan.

Ryo Sasaki (R)

Division of Pathological Biochemistry, Tottori University Faculty of Medicine, Yonago, Japan.

Tetsuya Yumioka (T)

Division of Urology, Tottori University Faculty of Medicine, Yonago, Japan.

Hideto Iwamoto (H)

Division of Urology, Tottori University Faculty of Medicine, Yonago, Japan.

Panagiota Tsounapi (P)

Division of Urology, Tottori University Faculty of Medicine, Yonago, Japan.

Shuichi Morizane (S)

Division of Urology, Tottori University Faculty of Medicine, Yonago, Japan.

Katsuya Hikita (K)

Division of Urology, Tottori University Faculty of Medicine, Yonago, Japan.

Mitsuhiko Osaki (M)

Division of Pathological Biochemistry, Tottori University Faculty of Medicine, Yonago, Japan.
Chromosome Engineering Research Center, Tottori University Faculty of Medicine, Yonago, Japan.

Futoshi Okada (F)

Division of Pathological Biochemistry, Tottori University Faculty of Medicine, Yonago, Japan.
Chromosome Engineering Research Center, Tottori University Faculty of Medicine, Yonago, Japan.

Atsushi Takenaka (A)

Division of Urology, Tottori University Faculty of Medicine, Yonago, Japan.

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Classifications MeSH