Paglia Donald E, Tsu I-Hsien
University of California, Los Angeles, Hematology Research Laboratory, Department of Pathology and Laboratory Medicine, California 90095-1732, USA
J Zoo Wildl Med. 2012 Sep;43(3 Suppl):S92-104. doi: 10.1638/2011-0177.1.
Necropsies of two browser rhinoceroses, African black (Diceros bicornis) and Sumatran (Dicerorhinus sumatrensis), often reveal extensive iron-pigment deposition in various tissues. This condition (hemosiderosis) has not been observed in species that are natural grazers, African white (Ceratotherium simum) and Asian greater one-horned (Indian; Rhinoceros unicornis), nor in any species free ranging in the wild. The causes, clinical significance, and consequences of captivity-acquired hemosiderosis have remained controversial despite two decades of compelling evidence that iron tends to accumulate logarithmically in all members of affected species in proportion to periods of expatriation; total-body iron loads can reach 10-fold in less than 3 yr and eventually exceed reference ranges by two to three orders of magnitude; iron overburdens are accompanied by laboratory and histopathologic evidence of cellular injury, necrosis and other clinical consequences characteristic of chronic pathologic iron storage [corrected] disorders (ISD) in humans and other species (hemochromatosis); and that ISD develops in many other exotic wildlife species displaced from their natural habitats. The historical evolution of evidence establishing the development of pathologic ISD in browser (but not in grazer) rhinoceroses and the possible relevance of ISD to other conditions affecting these two species will be reviewed. Evidence reviewed includes new as well as published data derived from quantitative measurements of iron analytes in sera and necropsy tissues and histopathologic evaluations of current and past necropsies of captive and free-ranging rhinoceroses of all four available species. The evolutionary, husbandry, and conservation implications of ISD in rhinoceroses are relevant to understanding ISD acquired by many other species of exotic wildlife when displaced from their natural environments.
对两只食叶犀牛——非洲黑犀(双角犀属)和苏门答腊犀(苏门答腊犀属)进行尸检时,常常会发现各种组织中有广泛的铁色素沉积。这种情况(血色素沉着症)在天然食草动物物种——非洲白犀(白犀属)和亚洲大独角犀(印度犀;独角犀属)中未被观察到,在任何野生放养的物种中也未被观察到。尽管有二十年的有力证据表明,铁往往会在受影响物种的所有个体中按照流放时间呈对数积累;全身铁负荷在不到3年的时间内可达到10倍,最终超过参考范围两到三个数量级;铁过载伴随着细胞损伤、坏死以及人类和其他物种慢性病理性铁储存[校正后]疾病(ISD)(血色素沉着症)特征性的其他临床后果的实验室和组织病理学证据;并且ISD在许多其他从其自然栖息地流离失所的外来野生动物物种中也会发生,但圈养获得性血色素沉着症的病因、临床意义和后果仍存在争议。本文将回顾确立食叶(而非食草)犀牛病理性ISD发展的证据的历史演变以及ISD与影响这两个物种的其他状况的可能相关性。所回顾的证据包括来自血清和尸检组织中铁分析物定量测量的新数据以及已发表的数据,以及对所有四个现有物种的圈养和野生放养犀牛当前和过去尸检的组织病理学评估。犀牛中ISD的进化、饲养和保护意义与理解许多其他外来野生动物物种在从其自然环境中流离失所时获得的ISD相关。