Skip to main content
Regenerative Therapy logoLink to Regenerative Therapy
letter
. 2019 Jun 12;11:73–74. doi: 10.1016/j.reth.2019.05.005

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

Ryo Sasaki 1,2,3,4,5,, Hajime Matsumine 1,2,3,4,5, Yorikatsu Watanabe 1,2,3,4,5, Tomohiro Ando 1,2,3,4,5, Masayuki Yamato 1,2,3,4,5
PMCID: PMC6562832  PMID: 31223635

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.

Fig. 1

Schematic diagram of the cage cleaning method.

Conflicts of interest

The authors declare no conflicts of interest.

Acknowledgements

We are indebted to Ms. Hallie Thorp, University of Utah, for technical review.

Footnotes

Peer review under responsibility of the Japanese Society for Regenerative Medicine.

References

  • 1.Burn C.C., Peters A., Day M.J., Mason G.J. Long-term effects of cage-cleaning frequency and bedding type on laboratory rat health, welfare, and handleability: a cross-laboratory study. Lab Anim. 2006;40:353–370. doi: 10.1258/002367706778476460. [DOI] [PubMed] [Google Scholar]
  • 2.Sasaki R., Aoki S., Yamato M., Uchiyama H., Wada K., Ogiuchi H. PLGA artificial nerve conduits with dental pulp cells promote facial nerve regeneration. J Tissue Eng Regenerat Med. 2011;5:823–830. doi: 10.1002/term.387. [DOI] [PubMed] [Google Scholar]
  • 3.Sasaki R., Aoki S., Yamato M., Uchiyama H., Wada K., Okano T. Tubulation with dental pulp cell promotes facial nerve regeneration in rats. Tissue Eng Part A. 2008;14:1141–1147. doi: 10.1089/ten.tea.2007.0157. [DOI] [PubMed] [Google Scholar]
  • 4.Sasaki R., Matsumine H., Watanabe Y., Takeuchi Y., Yamato M., Okano T. Electrophysiological and functional evaluations of regenerated facial-nerve defect with a tube containing dental pulp cells in rats. Plast Reconstr Surg. 2014;134:970–978. doi: 10.1097/PRS.0000000000000602. [DOI] [PubMed] [Google Scholar]
  • 5.Watanabe Y., Sasaki R., Matsumine H., Yamato M., Okano T. Undifferentiated and differentiated adipose-derived stem cells improve nerve regeneration in a rat model of facial nerve defect. J Tissue Eng Regenerat Med. 2017;11:362–374. doi: 10.1002/term.1919. [DOI] [PubMed] [Google Scholar]
  • 6.Matsumine H., Sasaki R., Tabata Y., Matsui M., Yamato M., Okano T. Facial nerve regeneration using basic fibroblast growth factor-impregnated gelatin microspheres in a rat model. J Tissue Eng Regenerat Med. 2016;10:E559–E567. doi: 10.1002/term.1884. [DOI] [PubMed] [Google Scholar]
  • 7.Matsumine H., Sasaki R., Yamato M., Okano T., Sakurai H. A polylactic acid non-woven nerve conduit for facial nerve regeneration in rats. J Tissue Eng Regenerat Med. 2014;8:454–462. doi: 10.1002/term.1540. [DOI] [PubMed] [Google Scholar]

Articles from Regenerative Therapy are provided here courtesy of Japanese Society for Regenerative Medicine

RESOURCES