It has been previously established that hypophysectomy leads to renal atrophy in rats and that a crude pituitary-derived fraction is effective in restoring kidney weight to the level expected for intact animals of the same body weight. This paper reports that considerable purification of the crude renotropic fraction from ovine pituitaries has been achieved and that the purified fraction is capable of restoring kidney weights of hypophysectomized castrated rats to normal values. For example, after five daily subcutaneous injections (135 micrograms/day) there were significant increases in dry kidney weight and total renal protein and DNA. The pituitary-derived fraction was devoid of somatotropin, contained only trace amounts of corticotropin, gamma-lipotropin, vasopressin, and prolactin, and had only low levels of thyrotropin and follitropin. Daily injections of prolactin, thyrotropin, and follitropin in doses of 20 micrograms each failed to stimulate renal growth in hypophysectomized rats. Thus, it seems highly unlikely that these factors are responsible for the observed renal hyperplasia after treatment with the pituitary fraction. The purified renotropic fraction had an isoelectric pH between 8 and 9. On polyacrylamide gel electrophoresis in the presence of detergent and a reducing agent, the renotropic fraction exhibited two major bands and one minor band with mobilities that corresponded to those of a standard lutropin preparation. The renotropic fraction exhibited considerable crossreactivity with an antiserum directed against the lutropin alpha subunit, suggesting the presence of the common glycoprotein hormone subunit. Moreover, the purified fraction stimulated steroid production by Leydig tumor cells in vitro. It is noteworthy, however, that standard ovine lutropin at 135 micrograms/day failed to exhibit renotropic activity in hypophysectomized castrated rats, although effects were noted at twice that dose. It appears that the renotropic activity represents a pituitary substance that can be separated from lutropin only with difficulty.
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http://dx.doi.org/10.1073/pnas.79.21.6675 | DOI Listing |
J Endocrinol
October 1995
Institute of Experimental Clinical Research, Aarhus Kommunehospital, Denmark.
IGF-I acts as a renotropic factor in early streptozotocin-induced diabetes. Somatostatin analogue (octreotide) treatment initiated at the onset of diabetes prevents kidney IGF-I accumulation and renal growth. Seven days of octreotide treatment initiated after 3, 5, 7 or 9 days of untreated diabetes was investigated.
View Article and Find Full Text PDFExp Nephrol
February 1995
Metabolic Unit Research Laboratory, Fundación Jiménez Díaz, Madrid, Spain.
Using chromatographic techniques, we have purified a peptide responsible, at least in part, for the renotropic activity detected in 24-hour uninephrectomized adult rat plasma. The most purified material behaved as a single component when analyzed by reversed-phase HPLC. The purified factor stimulates DNA synthesis in isolated rat proximal tubules and proximal tubular cell (LLC-PK1) cultures.
View Article and Find Full Text PDFEndocr J
February 1993
Research and Development Center, Calpis Food Industry Co., Ltd., Tokyo, Japan.
Ovine luteinizing hormone (oLH), a pituitary hormone with sulfated asparagine-linked oligosaccharides, was examined with regard to how its isoforms having different isoelectric points (pIs) modulate in vivo biological activity. oLH was separated into five fractions by means of an isoelectric focusing (IEF) column, i.e.
View Article and Find Full Text PDFEndocrinology
February 1989
Department of Medicine, Tokyo Women's Medical College, Japan.
We recently demonstrated the renotropic activity in ovine LH isoform(s). In this study we purified porcine (p) LH isoforms and analyzed their structures and bioactivities. Purified pLH preparation (G-100 fraction 3) was dissociated into alpha- and beta-subunits, followed by isolation with reverse phase HPLC.
View Article and Find Full Text PDFEndocrinology
August 1988
Department of Medicine, Tokyo Women's Medical College, Japan.
Renotropic activity was previously demonstrated in an ovine LH preparation. This preparation was further purified with a series of chromatographic steps, and the fractions were assayed for renotropic activity in vivo by their ability to stimulate [3H]thymidine incorporation into renal DNA of castrated hypophysectomized male rats. A purified preparation could be dissociated by acid treatment into two major constituent subunits, designated alpha and beta, each of which was composed of three microheterogeneous components (subunits alpha 1-3 and beta 1-3) by reverse phase HPLC.
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