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全身给药诱导大鼠下颌下腺2型胱抑素的表达

Induction of type 2 cystatin in rat submandibular glands by systemically administered agents.

作者信息

Cohen R E, Neiders M E, Bedi G S, Comeau R

机构信息

Department of Periodontology, State University of New York, Buffalo 14214.

出版信息

Arch Oral Biol. 1993 Apr;38(4):319-25. doi: 10.1016/0003-9969(93)90139-d.

Abstract

An inducible type 2 cystatin has earlier been characterized in submandibular glands and kidneys of rats treated with isoproterenol, as well as in kidneys of rats with experimental renal disease. The purpose now was to determine whether giving agents that have systemic toxicity could also be associated with induction of cystatin in rat salivary glands. Female Wistar rats (200-250 g) were given isoproterenol, cyclocytidine, potassium dichromate or turpentine oil. After autopsy, the organs were sectioned, fixed in 10% formalin, and processed routinely. Paraffin sections were processed for both the peroxidase-antiperoxidase and the avidin-biotin-alkaline phosphatase immunocytochemical methods. The submandibular glands of rats given cyclocytidine had generalized, strong staining of acinar cells, as well as occasional weak staining within granular convoluted tubules. Animals given either potassium dichromate or turpentine oil exhibited moderate staining for cystatin in submandibular acini. Rats given isoproterenol as a positive control exhibited strong acinar staining throughout the submandibular gland, while the glands of untreated rats were unreactive. Inducible type 2 cystatin could not be detected in the parotid or sublingual glands, or in trachea, lung, stomach, small intestine, large intestine, spleen, liver and pancreas, after treatment with any of the systemic agents evaluated. The results indicate that elaboration of type 2 cystatin can be induced by a variety of systemically administered agents other than isoproterenol, and suggest that elaboration of type 2 cystatin may represent a more generalized response to tissue injury.

摘要

此前已在接受异丙肾上腺素治疗的大鼠下颌下腺和肾脏以及患有实验性肾脏疾病的大鼠肾脏中鉴定出一种可诱导的2型胱抑素。现在的目的是确定给予具有全身毒性的药物是否也会诱导大鼠唾液腺中胱抑素的产生。给雌性Wistar大鼠(200 - 250克)注射异丙肾上腺素、环胞苷、重铬酸钾或松节油。尸检后,将器官切片,用10%福尔马林固定,并进行常规处理。石蜡切片采用过氧化物酶 - 抗过氧化物酶和抗生物素蛋白 - 生物素 - 碱性磷酸酶免疫细胞化学方法处理。给予环胞苷的大鼠下颌下腺腺泡细胞呈现广泛、强烈的染色,在颗粒曲管内偶尔也有弱阳性染色。给予重铬酸钾或松节油的动物下颌下腺腺泡中胱抑素呈中度染色。作为阳性对照给予异丙肾上腺素的大鼠整个下颌下腺腺泡呈现强烈染色,而未处理大鼠的腺体无反应。在用所评估的任何一种全身药物处理后,在腮腺、舌下腺、气管、肺、胃、小肠、大肠、脾脏、肝脏和胰腺中均未检测到可诱导的2型胱抑素。结果表明,除异丙肾上腺素外,多种全身给药药物均可诱导2型胱抑素的产生,提示2型胱抑素的产生可能代表对组织损伤更普遍的反应。

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