Leibowitz H M, Morello S, Stern M, Kupferman A
Department of Ophthalmology, University School of Medicine, Boston, MA 02118.
Arch Ophthalmol. 1990 May;108(5):734-7. doi: 10.1001/archopht.1990.01070070120048.
A 9-mm perforating corneal wound was created in one eye of New Zealand albino rabbits, sutured, and treated with mouse-derived epidermal growth factor (1 mg/L), human-derived epidermal growth factor (1.0 mg/L to 100 mg/L), or buffered saline, instilled once, twice, or four times daily. Both mouse-derived epidermal growth factor and human-derived epidermal growth factor significantly increased the tensile strength of full-thickness corneal wounds after 9 days of topical therapy. For human-derived epidermal growth factor, a concentration of 10 mg/L administered twice daily produced the maximal effect. An increase in either the concentration of epidermal growth factor or its frequency of administration failed to induce a further increase in wound strength. Indeed, at a concentration of 100 mg/L, human-derived epidermal growth factor appeared to lose its ability to accelerate healing of full-thickness corneal wounds.
在新西兰白化兔的一只眼睛上制造一个9毫米的角膜穿孔伤口,进行缝合,然后用小鼠源性表皮生长因子(1毫克/升)、人源性表皮生长因子(1.0毫克/升至100毫克/升)或缓冲盐水进行治疗,每天滴注一次、两次或四次。局部治疗9天后,小鼠源性表皮生长因子和人源性表皮生长因子均显著提高了全层角膜伤口的抗张强度。对于人源性表皮生长因子,每天两次给予10毫克/升的浓度产生最大效果。表皮生长因子浓度或给药频率的增加均未能进一步提高伤口强度。事实上,在100毫克/升的浓度下,人源性表皮生长因子似乎失去了加速全层角膜伤口愈合的能力。