Roberts P, McGeachie J K
Department of Anatomy and Human Biology, University of Western Australia.
J Anat. 1992 Aug;181 ( Pt 1)(Pt 1):101-11.
The beta-antagonist (blocker) propranolol was tested for its effects on satellite cell proliferation and the revascularisation and regeneration of transplanted skeletal muscles. Utilising autoradiographic techniques it was found that there was no difference in the actual timing of onset of satellite cell activation between propranolol-treated and control mice. However, the numbers of proliferating myogenic cells were substantially reduced in the propranolol-treated mice until revascularisation of these transplants began, about 24 h later than in the controls; myogenesis was therefore retarded by propranolol. When transplants from propranolol-treated and control mice which had been allowed to regenerate for 14 d were analysed morphometrically it was found that there was no significant difference in the size of the transplants, although propranolol induced the formation of substantial lipid deposition in the central transplant region; this was evidence of inhibited revascularisation in the early stages (up to 4 d) after transplantation.
对β-拮抗剂(阻滞剂)普萘洛尔进行了测试,以观察其对卫星细胞增殖以及移植骨骼肌的血管再生和再生的影响。利用放射自显影技术发现,普萘洛尔处理的小鼠和对照小鼠之间卫星细胞激活开始的实际时间没有差异。然而,在普萘洛尔处理的小鼠中,增殖性肌原细胞的数量大幅减少,直到这些移植组织开始血管再生,比对照组晚约24小时;因此,普萘洛尔延缓了肌生成。当对普萘洛尔处理的小鼠和对照小鼠经14天再生后的移植组织进行形态计量分析时发现,移植组织的大小没有显著差异,尽管普萘洛尔在移植组织的中央区域诱导形成了大量脂质沉积;这证明了移植后早期(长达4天)血管再生受到抑制。