首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Erythropoietic Porphyria of the Fox Squirrel Sciurus niger
【2h】

Erythropoietic Porphyria of the Fox Squirrel Sciurus niger

机译:狐狸松鼠黑松鼠的造血卟啉症

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Uroporphyrin I is found in high concentration in the bones, teeth, blood, soft tissues, and urine of the fox squirrel, Sciurus niger. The concentration of uroporphyrin in fox squirrel spleen is much higher than in liver, kidney or bone marrow, probably because of accumulation from phagocytosed red cells. Bleeding causes a marked increase in the uroporphyrin concentration of red cells and spleen, and a 3-8-fold increase in uroporphyrin excretion. Urinary excretion of δ-aminolevulinic acid and porphobilinogen is not greater in fox squirrels than in nonporphyric gray squirrels. Sciurus carolinensis, used as controls. In all these characteristics, as well as in the previously demonstrated deficiency of the enzyme uroporphyrinogen III cosynthetase in red cells, the physiological porphyria of fox squirrels resembles congenital erythropoietic porphyria, a hereditary disease of man and cattle. For squirrels differ in showing no evidence of cutaneous photosensitivity or hemolytic anemia.Uroporphyrinogen III cosynthetase activity is present in fox squirrel bone marrow at 1/10 its concentration in gray squirrel marrow. The fox squirrel enzyme is much more unstable than the gray squirrel enzyme, which provides a possible explanation for its low activity and for the overproduction of uroporphyrin I. It is unlikely that the deficiency of cosynthetase is due to its inactivation by excessive amounts of uroporphyrinogen I synthetase, because activity of the latter enzyme is the same in blood from fox and gray squirrels.Fox squirrel porphyria provides a convenient model for studies of pathogenesis of human congenital erythropoietic porphyria.
机译:尿卟啉I高浓度存在于狐松鼠黑松鼠的骨骼,牙齿,血液,软组织和尿液中。狐松鼠脾脏中的尿卟啉浓度比肝脏,肾脏或骨髓中的尿卟啉浓度高得多,这可能是由于吞噬红细胞的积累。出血导致红细胞和脾的尿卟啉浓度显着增加,并且尿卟啉排泄增加3-8倍。狐狸松鼠中的δ-氨基乙酰丙酸和胆色素原的尿排泄不大于非卟啉灰鼠中的。鼠尾草carolinensis,用作对照。在所有这些特征中,以及先前证明的红细胞中的尿卟啉原酶III合成酶缺乏症,狐狸松鼠的生理性卟啉症类似于先天性红细胞生成性卟啉症,是人和牛的遗传性疾病。对于松鼠,不同之处在于没有显示出皮肤光敏性或溶血性贫血的证据。狐狸松鼠骨髓中存在尿卟啉原III合成酶活性,其浓度为灰松鼠骨髓的1/10。狐狸松鼠酶比灰松鼠酶不稳定得多,这为它的活性低和尿卟啉I过量提供了可能的解释。合成酶缺乏的可能性不大可能是由于过量的尿卟啉原I使它失活了。合成酶,因为后者的活性在狐狸和灰松鼠的血液中是相同的。狐狸鼠卟啉症为研究人类先天性促红细胞性卟啉症的发病机理提供了方便的模型。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号