» Articles » PMID: 6613533

Brain Lactic Acidosis and Ischemic Cell Damage: Quantitative Ultrastructural Changes in Capillaries of Rat Cerebral Cortex

Overview
Specialty Neurology
Date 1983 Jan 1
PMID 6613533
Citations 29
Authors
Affiliations
Soon will be listed here.
Abstract

Excessive tissue lactic acidosis has earlier been shown to aggravate structural damage of both neurons and glial cells in the rat cerebral cortex. To study the reactions of cortical capillaries, light- and electronmicroscopic morphometry was used. Rats were subjected to severe incomplete ischemia (cerebral blood flow below 5% of normal) for 30 min by clamping their carotid arteries and by lowering the blood pressure. Lactate production during ischemia was modified by preischemic administration of either saline (low lactic acidosis group) or glucose (high lactic acidosis group). In the animals with low lactic acidosis, only minimal vascular changes were seen after both 5 min and 90 min recirculation. In the high lactic acidosis group, the endothelial cells were swollen after 5 min of recirculation, and the changes grew markedly worse during 90 min of recirculation. Nuclear chromatin coarsened and mitochondria swelled up. Morphometry showed that the lumen narrowed as a result of endothelial swelling. In spite of variable degree of perivascular astrocytic edema, the outer capillary diameter was little changed in the experimental groups. It seems likely that endothelial swelling hampers postischemic circulation in incomplete ischemia accompanied by high lactic acidosis.

Citing Articles

Transcutaneous auricular vagus nerve stimulation improves cognitive decline by alleviating intradialytic cerebral hypoxia in hemodialysis patients: A fNIRS pilot study.

Wang M, Jin Y, He M, Zhou A, Zhu M, Lin F Heliyon. 2025; 10(21):e39841.

PMID: 39975458 PMC: 11838084. DOI: 10.1016/j.heliyon.2024.e39841.


Microenvironment-responsive nanosystems for ischemic stroke therapy.

Wu F, Zhang Z, Ma S, He Y, He Y, Ma L Theranostics. 2024; 14(14):5571-5595.

PMID: 39310102 PMC: 11413776. DOI: 10.7150/thno.99822.


The Role of Pericytes in Ischemic Stroke: Fom Cellular Functions to Therapeutic Targets.

Zhou S, Guo Z, Zhang D, Qu Y, Jin H Front Mol Neurosci. 2022; 15:866700.

PMID: 35493333 PMC: 9043812. DOI: 10.3389/fnmol.2022.866700.


Nomogram to predict hemorrhagic transformation for acute ischemic stroke in Western China: a retrospective analysis.

Zhang K, Luan J, Li C, Chen M BMC Neurol. 2022; 22(1):156.

PMID: 35468774 PMC: 9040382. DOI: 10.1186/s12883-022-02678-2.


Neurovascular Inflammaging in Health and Disease.

Meszaros A, Molnar K, Nogradi B, Hernadi Z, Nyul-Toth A, Wilhelm I Cells. 2020; 9(7).

PMID: 32635451 PMC: 7407516. DOI: 10.3390/cells9071614.


References
1.
Hansen A . The extracellular potassium concentration in brain cortex following ischemia in hypo- and hyperglycemic rats. Acta Physiol Scand. 1978; 102(3):324-9. DOI: 10.1111/j.1748-1716.1978.tb06079.x. View

2.
Zimmermann V, Hossmann K . Resuscitation of the monkey brain after one hour's complete ischemia. II. Brain water and electrolytes. Brain Res. 1975; 85(1):1-11. DOI: 10.1016/0006-8993(75)90997-x. View

3.
Rehncrona S, Rosen I, Siesjo B . Brain lactic acidosis and ischemic cell damage: 1. Biochemistry and neurophysiology. J Cereb Blood Flow Metab. 1981; 1(3):297-311. DOI: 10.1038/jcbfm.1981.34. View

4.
Siemkowicz E . Brain uptake of mannitol and sucrose after cerebral ischemia: effect of hyperglycemia. Acta Physiol Scand. 1981; 112(4):359-63. DOI: 10.1111/j.1748-1716.1981.tb06831.x. View

5.
Ames 3rd A, Wright R, Kowada M, THURSTON J, Majno G . Cerebral ischemia. II. The no-reflow phenomenon. Am J Pathol. 1968; 52(2):437-53. PMC: 2013326. View