» Articles » PMID: 7435162

Hypothalamic Lesions in Rats with Long-term Streptozotocin-induced Diabetes Mellitus. A Semiquantitative Light- and Electron-microscopic Study

Overview
Specialty Neurology
Date 1980 Jan 1
PMID 7435162
Citations 13
Authors
Affiliations
Soon will be listed here.
Abstract

Sixteen male Wistar rats, 1 year after injection of streptozotocin or vehicle, were fixed by whole-body perfusion, the brains were removed and processed for light and electron microscopy. Study of semithin sections from the hypothalamic area revealed changes in the arcuate nucleus and median eminence. The lesions, in comparison with controls, were subjected to a blind semiquantitative evaluation. The following changes were observed by light microscopy in diabetic rats: accumulation of glycogen (P < 0.01), degeneration of neurons (P < 0.05), hypotrophy of tanycytes (P < 0.01), and axonal changes. Electron microscopy of diabetic rats revealed that glycogen was increased in neuronal bodies and processes (axons, synapses), also in tanycytes, and glia cells. In neurons were seen: dilated and fragmented endoplasmic reticulum, degranulated ergastoplasm, loss of organelles, increased number of microtubuli, myelin figures, irregularities in the form of nuclei, and appearance of chromatin. The tanycytes in diabetic animals were reduced in volume, had an increased nuclear cytoplasmic ratio, a reduced number of organelles, short basal processes, and almost complete loss of the apical processes. These changes demonstrate the existence, under experimental conditions, of an encephalopathy pathogenetically related to streptozotocin-induced diabetes.

Citing Articles

TSPO: an emerging role in appetite for a therapeutically promising biomarker.

Wang J, Beecher K Open Biol. 2021; 11(8):210173.

PMID: 34343461 PMC: 8331234. DOI: 10.1098/rsob.210173.


Changing shapes of glycogen-autophagy nexus in neurons: perspective from a rare epilepsy.

Singh P, Singh S Front Neurol. 2015; 6:14.

PMID: 25699013 PMC: 4316721. DOI: 10.3389/fneur.2015.00014.


Deleterious effects of neuronal accumulation of glycogen in flies and mice.

Duran J, Tevy M, Garcia-Rocha M, Calbo J, Milan M, Guinovart J EMBO Mol Med. 2012; 4(8):719-29.

PMID: 22549942 PMC: 3494072. DOI: 10.1002/emmm.201200241.


Effects of glucose, insulin, and supernatant from pancreatic beta-cells on brain-pancreas relative protein in rat hippocampus.

Lin Y, Westenbroek C, Tie L, Liu A, Yu H, Ter Horst G Neurochem Res. 2006; 31(12):1417-24.

PMID: 17091403 DOI: 10.1007/s11064-006-9193-9.


Hippocampal neuropathology of diabetes mellitus is relieved by estrogen treatment.

Saravia F, Beauquis J, Revsin Y, Homo-Delarche F, de Kloet E, De Nicola A Cell Mol Neurobiol. 2006; 26(4-6):943-57.

PMID: 16807785 PMC: 11520735. DOI: 10.1007/s10571-006-9096-y.


References
1.
Scott D, Paull W . The tanycyte of the rat median eminence. I. Synaptoid contacts. Cell Tissue Res. 1979; 200(2):329-34. DOI: 10.1007/BF00236425. View

2.
Brawer J, Lin P, Sonnenschein C . Morphological plasticity in the wall of the third ventricle during the estrous cycle in the rat: a scanning electron microscopic study. Anat Rec. 1974; 179(4):481-90. DOI: 10.1002/ar.1091790408. View

3.
Olsson Y, SOURANDER P, Angervall L . A patho-anatomical study of the central and peripheral nervous system in diabetes of early onset and long duration. Pathol Eur. 1968; 3(1):62-79. View

4.
Junod A, Lambert A, Orci L, Pictet R, Gonet A, Renold A . Studies of the diabetogenic action of streptozotocin. Proc Soc Exp Biol Med. 1967; 126(1):201-5. DOI: 10.3181/00379727-126-32401. View

5.
Reske-Nielsen E, Lundbaek K . DIABETIC ENCEPHALOPATHY. DIFFUSE AND FOCAL LESIONS OF THE BRAIN IN LONG-TERM DIABETES. Acta Neurol Scand Suppl. 1963; 39(4):SUPPL4:273-90. View