Research Article| January 01 1970 The Madeira Cockroach as an Experimental Animal William J. Yurkiewicz William J. Yurkiewicz Search for other works by this author on: This Site PubMed Google Scholar The American Biology Teacher (1970) 32 (1): 39. https://doi.org/10.2307/4442886 Views Icon Views Article contents Figures & tables Video Audio Supplementary Data Peer Review Share Icon Share Facebook Twitter LinkedIn MailTo Tools Icon Tools Get Permissions Cite Icon Cite Search Site Citation William J. Yurkiewicz; The Madeira Cockroach as an Experimental Animal. The American Biology Teacher 1 January 1970; 32 (1): 39. doi: https://doi.org/10.2307/4442886 Download citation file: Ris (Zotero) Reference Manager EasyBib Bookends Mendeley Papers EndNote RefWorks BibTex toolbar search Search Dropdown Menu toolbar search search input Search input auto suggest filter your search All ContentThe American Biology Teacher Search This content is only available via PDF. Copyright 1970 The National Association of Biology Teachers Article PDF first page preview Close Modal You do not currently have access to this content.
The anabolic effects of testosterone on kidneys from two strains of female mice were studied over a course of 25 days. The A/J and C57BL/6J strains were selected because they carry regulatory alleles Gur a and Gur b which determine rapid and slow induction of β‐glucuronidase, respectively. (A major goal of this study was to determine whether these mouse strains have other differences in their responses to testosterone). The wet weight, dry weight and total protein content of the kidneys of both strains increased about 70% in both strains. Total RNA increased 112% and 93% in a biphasic manner in the A/J and C57BL/6J mouse strains, respectively. The steep slope during the first 5 to 7 days was attributed to a selective stimulation of RNA accumulation while the latter, less rapid, RNA increase occurred in parallel with tissue growth. The total DNA content of kidneys from testosterone treated A/J mice never increased above that of controls, indicating that hypertrophy could account for renal enlargement in this strain. By contrast, testosterone treatment produced a 24% increase in total kidney DNA in C57BL/6J mice, signifying that both hypertrophy and hyperplasia are important factors in the anabolic response of this strain. These observations indicated another difference in the androgen induced response of A/J and C57BL/6J mice. As a consequence of the testosterone stimulated increase in renal β‐glucu‐ronidase synthesis, the excretion of the lysosomal form of the enzyme into the urine increased 2200‐fold in A/J but only 57‐fold in C57BLIGJ. The total enzyme activity excretedidayimouse was only 4 times higher in A/J versus C57BLi6J with the differences reflecting the basal activity which was 10‐fold higher in C57BLIGJ mice. The basal excretion of another lysosomal enzyme, β‐galactosidase, was also several fold higher in C57BL/6J, suggesting that lysosomes in those animals are either larger or their contents are excreted at a faster rate.
