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Panlab morris water maze test
Therapeutic effect of ERCM on behavioral functions in cerebral palsy animal model. (A) Use ratio (%) of forelimb contralateral to hypoxia-ischemia-lipopolysaccharide injection (HIL) in the cylinder <t>test</t> at postnatal day (PND) 10, 20, 30, and 40. Rats ( n = 7 per group) were subjected to HIL, and injected ERCM once at only PND7 in the single-dose groups (1.5 × 10 10 and 6.0 × 10 10 ), or repeatedly at PND7, 17, 27, and 37 in repeated-dose group (6.0 × 10 10 ) via the tail vein. (B) Latency time (s) in rotarod performance at PND10, 20, 30, and 40. The speed of the rotarod was progressively increased: 2 rpm at PND10, 10 rpm at PND20, and 25 rpm at both PND30 and PND40. (C) Passive avoidance test and (D) <t>Morris</t> <t>water</t> <t>maze</t> test were conducted once daily from PND41 to PND45 to assess learning and memory functions. (E) Representative tracking images in the Morris water maze test. One-way ANOVA with Tukey’s multiple-comparison test (mean ± SD). # Significantly different from normal control ( P < .05). *Significantly different from vehicle control ( P < .05).
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Therapeutic effect of ERCM on behavioral functions in cerebral palsy animal model. (A) Use ratio (%) of forelimb contralateral to hypoxia-ischemia-lipopolysaccharide injection (HIL) in the cylinder test at postnatal day (PND) 10, 20, 30, and 40. Rats ( n = 7 per group) were subjected to HIL, and injected ERCM once at only PND7 in the single-dose groups (1.5 × 10 10 and 6.0 × 10 10 ), or repeatedly at PND7, 17, 27, and 37 in repeated-dose group (6.0 × 10 10 ) via the tail vein. (B) Latency time (s) in rotarod performance at PND10, 20, 30, and 40. The speed of the rotarod was progressively increased: 2 rpm at PND10, 10 rpm at PND20, and 25 rpm at both PND30 and PND40. (C) Passive avoidance test and (D) Morris water maze test were conducted once daily from PND41 to PND45 to assess learning and memory functions. (E) Representative tracking images in the Morris water maze test. One-way ANOVA with Tukey’s multiple-comparison test (mean ± SD). # Significantly different from normal control ( P < .05). *Significantly different from vehicle control ( P < .05).

Journal: Stem Cells Translational Medicine

Article Title: Therapeutic effect of amniotic membrane mesenchymal stem cell-derived exosome-rich conditioned medium in cerebral palsy model

doi: 10.1093/stcltm/szaf071

Figure Lengend Snippet: Therapeutic effect of ERCM on behavioral functions in cerebral palsy animal model. (A) Use ratio (%) of forelimb contralateral to hypoxia-ischemia-lipopolysaccharide injection (HIL) in the cylinder test at postnatal day (PND) 10, 20, 30, and 40. Rats ( n = 7 per group) were subjected to HIL, and injected ERCM once at only PND7 in the single-dose groups (1.5 × 10 10 and 6.0 × 10 10 ), or repeatedly at PND7, 17, 27, and 37 in repeated-dose group (6.0 × 10 10 ) via the tail vein. (B) Latency time (s) in rotarod performance at PND10, 20, 30, and 40. The speed of the rotarod was progressively increased: 2 rpm at PND10, 10 rpm at PND20, and 25 rpm at both PND30 and PND40. (C) Passive avoidance test and (D) Morris water maze test were conducted once daily from PND41 to PND45 to assess learning and memory functions. (E) Representative tracking images in the Morris water maze test. One-way ANOVA with Tukey’s multiple-comparison test (mean ± SD). # Significantly different from normal control ( P < .05). *Significantly different from vehicle control ( P < .05).

Article Snippet: To evaluate spatial memory, rats were subjected to the Morris water maze test (Smart v2.5; Panlab Technology).

Techniques: Animal Model, Injection, Comparison, Control