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Optimal Dose and Timing of Umbilical Stem Cells Treatment in Pulmonary Arterial Hypertensive Rats
Yonsei med. j ; Yonsei med. j;: 570-580, 2017.
Article en En | WPRIM | ID: wpr-188812
Biblioteca responsable: WPRO
ABSTRACT
PURPOSE: Pulmonary arterial hypertension (PAH) is a fatal disease which is characterized by an increase in pulmonary arterial pressure leading to increases in right ventricular afterload. Human umbilical cord blood derived-mesenchymal stem cells (hUCB-MSCs) administered via the jugular vein have been previously shown to improve PAH by reversal treatment. However, the effect of low dosage and transfusion timing of hUCB-MSCs on PAH has not yet been clearly established. Obviously, low dosage treatment can lead to a reduction in costs. This is the first study on early transfusion effect. MATERIALS AND METHODS: This study was divided into two parts. The first part is an investigation of dose-dependent effect. hUCB-MSCs were administered into 3 groups of rats (UA: 3×10⁶ cells, UB: 1.5×10⁶ cells, UC: 3×10⁵ cells) via the external jugular vein at week 1 after monocrotaline (MCT) injection. The second part is a search for optimal treatment timing in 3×10⁵ cells dose of hUCB-MSCs administered at day 1 for UD group (low dose of hUCB-MSCs at day 1), at day 1 and week 1 for the UE group (dual transfusion of low dose of hUCB-MSCs at day 1 and week 1) and at 1 week for the UF group (reversal treatment of low dose hUCB-MSC at week 1) after MCT injection. RESULTS: The administration of 3×10⁵ hUCB-MSCs was as effective as the 3×10⁶ dose in decreasing mean right ventricle (RV) pressure and pulmonary pathological changes. Early treatment with hUCB-MSCs improved mean RV pressure, pulmonary pathological changes and heart collagen 3 protein expression levels in PAH. CONCLUSION: Low-dose early treatment of hUCB-MSCs is as effective as a high dose treatment of hUCB-MSCs in improving PAH although dual or reversal treatment is still more effective.
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Texto completo: 1 Índice: WPRIM Asunto principal: Células Madre / Colágeno / Monocrotalina / Sangre Fetal / Células Madre Mesenquimatosas / Presión Arterial / Corazón / Ventrículos Cardíacos / Hipertensión / Hipertensión Pulmonar Límite: Animals / Humans Idioma: En Revista: Yonsei med. j Año: 2017 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Asunto principal: Células Madre / Colágeno / Monocrotalina / Sangre Fetal / Células Madre Mesenquimatosas / Presión Arterial / Corazón / Ventrículos Cardíacos / Hipertensión / Hipertensión Pulmonar Límite: Animals / Humans Idioma: En Revista: Yonsei med. j Año: 2017 Tipo del documento: Article