The DOI matches its Crossref record.
Glycosidase Activities in the Liver and Kidney of Hereditary Diabetic Mice
Abstract
Hereditary diabetic mice (NSY) were inbred from original streptozotocin diabetic ICR mice for 8-9 generations using hyperglycemia as an index. The normoglycemic ICR mice were used as controls for the NSY line. The nonfasting blood sugar level of the NSY mice was 305 +/- 14 mg/100ml, while their immunoreactive insulin level was 30 +/- 4 microU/ml (the values of the controls were 165 +/- 12 mg/100 ml and 79 +/- 14 microU/ml, respectively). beta-N-Acetylglucosaminidase [EC 3.2.1.29], beta-galactosidase [EC 3.2.1.23], alpha-glucosidase [EC 3.2.1.21], and alpha-mannosidase [EC 3.2.1.24] activities were determined in the 1,000 X g supernatant of the liver and the kidney of control and streptozotocin diabetic ICR mice and their NSY line. In the kidneys of the insulinopenic NSY mice, the beta-galactosidase and alpha-mannosidase activities were significantly decreased. No significant changes were found in liver enzyme activities. Insulin treatment increased the kidney beta-galactosidase activity signficantly. The insulinopenic state, which caused a decrease in the glycosidase activities in the kidney, could induce retarded breakdown of glycoprotein.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“In both flies and humans, changes in expression and activity levels of α-mannosidases have been linked to impairments in insulin signaling and glucose metabolism (66–70).”
From Corazonin signaling integrates energy homeostasis and lunar phase to regulate aspects of growth and sexual maturation in Platynereis (2020) · cites this paper as [68]
Citations
Cited by
Sorted by citations
Andreatta, G., Broyart, C., Borghgraef, C., Vadiwala, K., Kozin, V., Polo, A., Bileck, A., Beets, I., Schoofs, L., Gerner, C., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1910262116 · Cited by 61
Mohanam, S., & Bose, S. M. (1983) · Diabetologia · doi:10.1007/bf00251900 · Cited by 24
“Decreased lysosomal enzyme activity in renal tissue of streptozotocin-diabetic rats [14] mice [13] and Chinese hamsters with spontaneous diabetes [6] shows that lysosomal enzyme deficiency could be involved in the genesis of renal microangiopathy.”
BackgroundInactivation of Bovine Kidney β-N-Acetyl-D-glucosaminidase by Nonenzymatic Glucosylation
DOLHOFER, R., SIESS, E. A., & WIELAND, O. H. (1982) · Hoppe-Seyler´s Zeitschrift für physiologische Chemie · doi:10.1515/bchm2.1982.363.2.1427 · Cited by 17
Selectively Bred Diabetes Models: GK Rats, NSY Mice, and ON Mice
Nagao, M., Esguerra, J. L. S., Wendt, A., Asai, A., Sugihara, H., Oikawa, S., & Eliasson, L. (2020) · Methods in molecular biology · doi:10.1007/978-1-0716-0385-7_3 · Cited by 16
The effects of parabiosis on serum and kidney glycosidase activities in spontaneously diabetic mice
Fushimi, H., Nonaka, K., Tarui, S., et al. (1980) · Diabetologia · doi:10.1007/bf00258311 · Cited by 16
“Marked decreases in the activities of a- and fi-glycosidases have been observed in the streptozotocin diabetic rat kidney [2-4], and a significant decrease in fi-galactosidase and a-mannosidase activities has been shown in kidneys of spontaneously mildly diabetic NSY mice [5].”
BackgroundSelf-citation
Metadata
- Authors
- FUSHIMI, H., SHIBATA, M., & TARUI, S.
- Affiliations
- Sumitomo Hospital (JP)
- Nagoya University (JP)
- The University of Osaka (JP)
- ORCID
- SHIBATA, Masao
- Venue
- The Journal of Biochemistry
- Publisher
- Oxford University Press (OUP)
- Published
- 1980-03
- Volume
- 87
- Issue
- 3
- Pages
- 941-949
- ISSN
- 0021-924X (ISSN-L)
- 1756-2651
- OpenAlex
- W1871937501
- Cited by
- 15
- References
- 0
- Citations by year
- 2020: 1 · 2019: 1 · 2018: 1 · 2017: 1
- FWCI
- 1.28
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Biochemistry (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Glycosylation and Glycoproteins Research
- Health Sciences › Medicine › Genetics (clinical) › Lysosomal Storage Disorders Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Glycogen Storage Diseases and Myoclonus
- Keywords
- hereditary diabetes, streptozotocin-induced diabetes, glycosidase activity, beta-galactosidase, alpha-mannosidase, N-acetyl-beta-D-glucosaminidase, alpha-glucosidase, insulin deficiency, insulin therapy, glycoprotein degradation, liver, kidney, hyperglycemia
- MeSH terms
- Animals, Diabetes Mellitus, Experimental, Glycoside Hydrolases, Kidney, Liver, Male, Mice, Inbred ICR, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review