Many neoplasms have been shown to induce capillary neovascularization and this may correlate with aggressive behavior. We investigated the phenomenon of neovascularity in benign and malignant prostatic tissue. Microvessel profiles and tissue sections were visualized by antibodies to Factor Vlll and
In vivo morphometric analysis of muscle microcirculation in dystrophic mice
β Scribed by Dr. Thomas G. Burch; Dr. Russell L. Prewitt; Dr. Peter K. Law
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 391 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0148-639X
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
In order to test the vascular hypothesis of muscular dystrophy, the gracilis muscle in 6hyphen; to 7hyphen;weekhyphen;old C57BL/6Jhyphen;dy^2J^ normal and dystrophic mice was studied using in vivo quantitative morphometric techniques to determine the total length and surface area of capillaries in which blood was flowing per unit volume of muscle. Individual capillary lengths, diameters, and red blood cell velocities were also quantified. During resting conditions, the capillary density (length per unit volume of muscle) and surface area are increased significantly in dystrophic muscle compared to normal muscle. Under fully vasodilated conditions, the capillary density and surface area are similar in normal and dystrophic muscle. Individual capillary lengths, diameters, and red blood cell velocities are also similar in normal and dystrophic muscle under resting conditions. These results indicate that, contrary to the vascular hypothesis, dystrophic muscle at rest has increased capillary density, surface area, and blood flow. It is postulated that the increased capillary density in dystrophic muscle at rest is secondary to muscle fiber breakdown.
π SIMILAR VOLUMES
In vivo 31P NMR studies of normal and dystrophic pectoralis muscles of chicks were carried out in the age group of 2 to 8 weeks. It was observed that the ratios [PCr]/[Pi] and [PCr]/[ATP] were essentially the same in both normal and dystrophic muscles. The cellular pH for normal muscles however, was
## Abstract Muscle from dystrophic (129 ReJ dy/dy) mice, aged 1, 2, 3, 4, and 6 months, was cocultured with normal embryonic mouse spinal cord. Cultures were scored for regeneration (myotubes) and differentiation (crossβstriated or contracting fibers) over a 28βday period. Although muscle from dyst
Information about changes in muscle composition has to date been primarily restricted to histological examination of biopsy samples or qualitative assessment of images obtained using avariety of techniques (e.g., ultrasound, CT, and MRI). We describe the development of a quantitative method for the