Literature DB >> 31223635

A cage cleaning method for researchers without a cage-washing machine or cage-washing staff.

Ryo Sasaki1,2,3,1,4, Hajime Matsumine2,3,1,4, Yorikatsu Watanabe3,1,4, Tomohiro Ando1,4, Masayuki Yamato4.   

Abstract

Entities:  

Keywords:  Cage wash; Cleaning; Rat

Year:  2019        PMID: 31223635      PMCID: PMC6562832          DOI: 10.1016/j.reth.2019.05.005

Source DB:  PubMed          Journal:  Regen Ther        ISSN: 2352-3204            Impact factor:   3.419


× No keyword cloud information.
Sir: Although cage-cleaning is necessary for a hygienic environment for rats [1], weekly cage-cleaning results in excessive physical and mental stress for researchers who also maintain a clinical practice, do not have a cage-washing machine, and do not have a dedicated cage-washing staff. Because of the number of rats per study and the long-term housing required, this physical and mental stress is exacerbated for investigators who study nerve regeneration [2], [3], [4], [5], [6], [7]. To improve this work, a fast and efficient rat cage-cleaning method was developed. In conventional methods, cages (size: 23 cm width × 40 cm length × 20 cm height) (Natsume Seisakusho, Tokyo, Japan) were washed with a brush with cleaning solution and rinsed with water as the first step. These cages were then sprayed with 0.2% sodium hypochlorite and rinsed with water. In our improved method, as the first step, (1) the inner and outer surfaces of the cage were washed with a brush with cleaning solution and rinsed with water as usual. After the inner surface was washed, the water with cleaning solution that remained in the cage (approximately 1 cm in depth) was transferred into the second cage. The first cage was temporarily stored in the sink without rinsing. (2) The inner surface of the second cage was washed with a brush, and the remaining water with cleaning solution was transferred into the third cage. The outer surface of the second cage was washed with a brush with cleaning solution, and stacked into the first cage. (3) These washing steps were repeated for a total of 6 cages and the water with solution was discarded after the 6th cage. Together, all cages were rinsed in a water shower. (4) This process was repeated for subsequent cages in sets of 6 (Fig. 1). The mean consuming times for washing 12 cages with our method and the conventional method were 589 ± 16 sec and 673 ± 13 sec, respectively (n = 7, unpaired t-test, p = 0.0017), indicating that our method was significantly faster than the conventional method (p < 0.01). This difference will be more significant and noticeable as the number of cages being washed is scaled up (e.g., washing thirty cages). Additionally, this method required less water and cleaning solution compared with the conventional procedure. Moreover, this method has the potential to reduce the physical and mental stress associated with the conventional washing method. Our method will contribute to the reduction of stress for researchers having to wash a large number of cages without a cage-washer or a cage-washing staff.
Fig. 1

Schematic diagram of the cage cleaning method.

Schematic diagram of the cage cleaning method.

Conflicts of interest

The authors declare no conflicts of interest.
  7 in total

1.  A polylactic acid non-woven nerve conduit for facial nerve regeneration in rats.

Authors:  Hajime Matsumine; Ryo Sasaki; Masayuki Yamato; Teruo Okano; Hiroyuki Sakurai
Journal:  J Tissue Eng Regen Med       Date:  2012-06-11       Impact factor: 3.963

2.  PLGA artificial nerve conduits with dental pulp cells promote facial nerve regeneration.

Authors:  Ryo Sasaki; Shunsuke Aoki; Masayuki Yamato; Hiroto Uchiyama; Keiji Wada; Hideki Ogiuchi; Teruo Okano; Tomohiro Ando
Journal:  J Tissue Eng Regen Med       Date:  2011-01-17       Impact factor: 3.963

3.  Long-term effects of cage-cleaning frequency and bedding type on laboratory rat health, welfare, and handleability: a cross-laboratory study.

Authors:  Charlotte C Burn; Alan Peters; Michael J Day; Georgia J Mason
Journal:  Lab Anim       Date:  2006-10       Impact factor: 2.471

4.  Undifferentiated and differentiated adipose-derived stem cells improve nerve regeneration in a rat model of facial nerve defect.

Authors:  Yorikatsu Watanabe; Ryo Sasaki; Hajime Matsumine; Masayuki Yamato; Teruo Okano
Journal:  J Tissue Eng Regen Med       Date:  2014-06-01       Impact factor: 3.963

5.  Electrophysiologic and functional evaluations of regenerated facial nerve defects with a tube containing dental pulp cells in rats.

Authors:  Ryo Sasaki; Hajime Matsumine; Yorikatsu Watanabe; Yuichi Takeuchi; Masayuki Yamato; Teruo Okano; Mariko Miyata; Tomohiro Ando
Journal:  Plast Reconstr Surg       Date:  2014-11       Impact factor: 4.730

6.  Tubulation with dental pulp cells promotes facial nerve regeneration in rats.

Authors:  Ryo Sasaki; Shunsuke Aoki; Masayuki Yamato; Hiroto Uchiyama; Keiji Wada; Teruo Okano; Hideki Ogiuchi
Journal:  Tissue Eng Part A       Date:  2008-07       Impact factor: 3.845

7.  Facial nerve regeneration using basic fibroblast growth factor-impregnated gelatin microspheres in a rat model.

Authors:  Hajime Matsumine; Ryo Sasaki; Yasuhiko Tabata; Makoto Matsui; Masayuki Yamato; Teruo Okano; Hiroyuki Sakurai
Journal:  J Tissue Eng Regen Med       Date:  2014-04-16       Impact factor: 3.963

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.