Twining S S, Zhou X, Schulte D P, Wilson P M, Fish B, Moulder J
Department of Biochemistry, Medical College of Wisconsin, Milwaukee, 53226, USA.
Invest Ophthalmol Vis Sci. 1996 Mar;37(4):511-22.
Vitamin A-deficient humans and animals are more susceptible to infections than are healthy humans and animals. This study compares the early corneal response (within 24 hours) to an experimental Pseudomonas aeruginosa infection between vitamin A deficient and control rats.
Male WAG/Rij/MCW rats were fed either a vitamin A- deficient diet (A-) or the same diet with retinyl palmitate added back in a nonrestricted manner (N) or under pair-fed conditions (A+) to yield weight-matched rats. Some A-rats were repleted wih retinyl palmitate 16 days before being killed and then given free access to the retinyl palmitate-supplemented diet (R). Twenty-four hours before being killed, the corneas of anesthetized rats were scratched and P. aeruginosa organisms were applied to the corneal surface. The rats were killed using an overdose of sodium pentobarbital. Corneas were either processed for light and electron microscopic examination or extracted for proteinase and myeloperoxidase determination. Corneal myeloperoxidase concentrations relative to neutrophil myeloperoxidase concentrations were used to determine the number of neutrophils in the cornea. Zymography was used to study caseinases, gelatinases, and plasminogen activators. Reverse zymography was used to detect proteinase inhibitors. Similar results were noted at early, mid, and late weight plateau stages of vitamin A deficiency.
Ulceration occurred within 24 hours when low numbers of P. aeruginosa (10(4) cpu) were applied topically onto scratched A- corneas, whereas no ulceration was observed in the A+, R, and N corneas. When higher numbers of P. aeruginosa (10(7)-10(8)) were applied to the scratched corneas, all corneas became ulcerated within 24 hours. The extent of ulceration in the control corneas was greater than that in A- corneas by a factor of two. Only the A- corneas contained inflammatory cells with unusual striated deposits in phagolysosomes. The total number of neutrophils in the cornea and the concentrations of caseinases, plasminogen activators, and gelatinases in the infected corneal extracts were similar; however, the concentrations of cysteine proteinase inhibitors were elevated under A- conditions.
Vitamin A deficiency alters the response of the cornea to a P. aeruginosa infection during the first 24 hours. The alterations observed are probably due to multiple factors: an insufficient tear film for bacterial clearance and migration of neutrophils, epithelial keratinization, alterations in corneal wound healing, and changes in polymorphonuclear function.
维生素A缺乏的人和动物比健康的人和动物更容易受到感染。本研究比较了维生素A缺乏的大鼠和对照大鼠对实验性铜绿假单胞菌感染的早期角膜反应(24小时内)。
雄性WAG/Rij/MCW大鼠分别喂食维生素A缺乏饮食(A-)或添加视黄醇棕榈酸酯的相同饮食,不限量(N)或配对喂养(A+)以获得体重匹配的大鼠。一些A-大鼠在处死前16天用视黄醇棕榈酸酯补充,然后自由获取补充视黄醇棕榈酸酯的饮食(R)。处死前24小时,麻醉大鼠的角膜被划伤,铜绿假单胞菌接种于角膜表面。大鼠过量注射戊巴比妥钠处死。角膜用于光镜和电镜检查,或提取用于蛋白酶和髓过氧化物酶测定。用角膜髓过氧化物酶浓度与中性粒细胞髓过氧化物酶浓度之比来确定角膜中中性粒细胞的数量。用酶谱法研究酪蛋白酶、明胶酶和纤溶酶原激活剂。用反向酶谱法检测蛋白酶抑制剂。在维生素A缺乏的早期、中期和晚期体重稳定阶段观察到类似结果。
当少量铜绿假单胞菌(10⁴cfu)局部接种于划伤的A-角膜时,24小时内发生溃疡,而A+、R和N组角膜未观察到溃疡。当大量铜绿假单胞菌(10⁷-10⁸)接种于划伤的角膜时,所有角膜在24小时内均发生溃疡。对照角膜的溃疡程度比A-角膜大两倍。只有A-角膜含有吞噬溶酶体中具有异常条纹状沉积物的炎性细胞。角膜中中性粒细胞总数以及感染角膜提取物中酪蛋白酶、纤溶酶原激活剂和明胶酶的浓度相似;然而,在A-条件下,半胱氨酸蛋白酶抑制剂的浓度升高。
维生素A缺乏在最初24小时内改变了角膜对铜绿假单胞菌感染的反应。观察到的改变可能是由于多种因素:用于细菌清除和中性粒细胞迁移的泪膜不足、上皮角质化、角膜伤口愈合改变以及多形核功能变化。