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Biomedical subjects

C Cintron

Publications and source records attributed to C Cintron.

49 records · Page 3Linked to original sources

The healing of linear nonperforating wounds in rabbit corneas of different ages.

Linear nonperforating incisions were made in the corneas of 2-week-old and 2-year-old rabbits. The resulting wounds were examined by light microscopy and transmission and scanning electron microscopy. A corneal incision of a 2-week-old rabbit produced a wide gaping wound caused by retraction of the cut stromal lamellae away from the incision. The wound became wider with time as the developing eye enlarged and the cut lamellae retracted further. Polymorphonuclear leukocytes, presumably from the tear film, penetrating into the wound area before it was covered over by the sliding epithelium. Most of the leukocytes disappeared by 3 days after wounding. Three to six layers of fibroblasts appeared beneath the epithelial plug. The tissue eventually rebuilt approximately one third of the corneal depth lost to the wound. The stroma of the wounded region did not return to its normal width, but the epithelium was thicker than that of the unwounded cornea. An incision in a 2-year-old rabbit cornea produced a narrow V-shaped wound that did not change shape with time. This wound was repaired by fibroblasts resulting in collagenous repair tissue being the same depth as the normal stroma. There appears to be no evidence for wide gaping wounds in humans in the literature, as was found in this study in rabbits.

Age Factors↗

Quantitative analysis of collagen from normal developing corneas and corneal scars.

We measured the relative solubility of collagen in acetic acid after pepsin digestion and tentatively identified the types of collagen present in corneas of rabbits of various ages and in corneal scar tissue, using hydroxyproline assays and polyacrylamide gel electrophoretic analyses. More than 80% of the collagen in normal developing rabbit cornea was soluble after pepsin treatment; no more than 45% of that in two-week-old corneal scars was soluble. The predominant collagens in normal cornea and healing tissue were types I and AB. Type AB increased from 6% of the total collagen in fetal cornea to 11% in cornea from young adults. Collagen from two-week-old corneal wounds contained 16% type AB. Corneal type AB collagen was less soluble and more resistant to degradation by mammalian collagenase than was type I collagen. Unlike the normal cornea, in healing tissue the relative rate of synthesis of type I to type AB collagens did not correspond to their deposition. These results suggest a basic alteration in the molecular structure of the corneal scar, which may be instrumental in preventing the healing tissue from producing a normal, functioning organ.

Age Factors↗

Quantitative studies of corneal epithelial wound healing in rabbits.

Corneal epithelial defects are covered rapidly by the movement of adjacent epithelium. However, the mechanism of this tissue movement is poorly understood. In this study, the quantity or cell water, protein, and DNA were determined in healing epithelium to test the hypothesis that cell enlargement contributes to the rapid coverage of the defect. In addition, light and transmission electron microscopy and [3H] thymidine incorporation into epithelial cells were used to determine whether the healing tissue moves as a unit or as individual cells. The quantitative determinations lead us to conclude that healing begins with a dramatic rise in cell water, followed by an increase in cell protein and finally by a gradual increase in DNA. The morphologic and autoradiographic evidence strongly suggests that large corneal epithelial defects in rabbits are covered by the movement of adjacent tissue as a unified, multilayered sheet of cells. Furthermore, the cells appear large than normal with minimal changes in intercellular spaces. We suggest that the increase in cell volume is due to water uptake, which plays an important role in covering the defect by increasing the cells' surface area. Protein is then accumulated, followed by cell proliferation.

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