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Efficacy and Safety of Human Bone Marrow-Derived Mesenchymal Stem Cells according to Injection Route and Dose in a Chronic Kidney Disease Rat Model.
Chae, Han Kyu; Suh, Nayoung; Jang, Myong Jin; Kim, Yu Seon; Kim, Bo Hyun; Aum, Joomin; Shin, Ha Chul; You, Dalsan; Hong, Bumsik; Park, Hyung Keun; Kim, Choung-Soo.
Afiliação
  • Chae HK; Department of Urology, Gangneung Asan Medical Center, University of Ulsan College of Medicine, Gangneung, Korea.
  • Suh N; Department of Pharmaceutical Engineering, College of Medical Sciences and Department of Medical Sciences, General Graduate School, Soon Chun Hyang University, Asan, Korea.
  • Jang MJ; Asan Institute for Life Sciences, Asan Medical Center, Seoul, Korea.
  • Kim YS; Department of Urology, Asan Medical Institute of Convergence Science and Technology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
  • Kim BH; Department of Urology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
  • Aum J; Department of Urology, Asan Medical Institute of Convergence Science and Technology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
  • Shin HC; Pharmicell Co. Ltd., Seongnam, Korea.
  • You D; Department of Urology, Asan Medical Institute of Convergence Science and Technology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
  • Hong B; Department of Urology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
  • Park HK; Department of Urology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
  • Kim CS; Department of Urology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Int J Stem Cells ; 16(1): 66-77, 2023 Feb 28.
Article em En | MEDLINE | ID: mdl-35483715
ABSTRACT
Background and

Objectives:

We compared the efficacy and safety of human bone marrow-derived mesenchymal stem cells (hBMSC), delivered at different doses and via different injection routes in an animal model of chronic kidney disease. Methods and

Results:

A total of ninety 12-week-old rats underwent 5/6 nephrectomy and randomized among nine groups sham, renal artery control (RA-C), tail vein control (TV-C), renal artery low dose (RA-LD) (0.5×106 cells), renal artery moderate dose (RA-MD) (1.0×106 cells), renal artery high dose (RA-HD) (2.0×106 cells), tail vein low dose (TV-LD) (0.5×106 cells), tail vein moderate dose (TV-MD) (1.0×106 cells), and tail vein high dose (TV-HD) (2.0×106 cells). Renal function and mortality of rats were evaluated after hBMSC injection. Serum blood urea nitrogen was significantly lower in the TV-HD group at 2 weeks (p<0.01), 16 weeks (p<0.05), and 24 weeks (p<0.01) than in the TV-C group, as determined by one-way ANOVA. Serum creatinine was significantly lower in the TV-HD group at 24 weeks (p<0.05). At 8 weeks, creatinine clearance was significantly higher in the TV-MD and TV-HD groups (p<0.01, p<0.05) than in the TV-C group. In the safety evaluation, we observed no significant difference among the groups.

Conclusions:

Our findings confirm the efficacy and safety of high dose (2×106 cells) injection of hBMSC via the tail vein.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies Idioma: En Revista: Int J Stem Cells Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies Idioma: En Revista: Int J Stem Cells Ano de publicação: 2023 Tipo de documento: Article