Localization of glucokinase gene expression in the rat brain

• Published in: Diabetes (New York, N.Y.) Vol. 49; no. 5; pp. 693 - 700
• Main Authors: Lynch, R M, Tompkins, L S, Brooks, H L, Dunn-Meynell, A A, Levin, B E
• Format: Journal Article
• Language: English
• Published: Alexandria, VA American Diabetes Association 01.05.2000
• Subjects: Animals; Arcuate Nucleus of Hypothalamus - metabolism; Base Sequence - genetics; Biochemistry and metabolism; Biological and medical sciences; Brain - metabolism; Brain - physiology; Brain chemistry; Central nervous system; Fundamental and applied biological sciences. Psychology; Gene Expression - physiology; Glucokinase - genetics; Gluconeogenesis; Hypothalamus - metabolism; In Situ Hybridization; Male; Metabolic regulation; Physiological aspects; Potassium Channels - metabolism; Potassium Channels, Inwardly Rectifying; Punctures; Rats; Rats, Sprague-Dawley; Regulation; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger - metabolism; Tissue Distribution; Vertebrates: nervous system and sense organs; Vertebrata; Mammalia; Rat; Enzyme; Transferases; Glucokinase; Rodentia; Central nervous system; Gene expression; Localization; Brain (vertebrata)
• ISSN: 0012-1797; 1939-327X
• DOI: 10.2337/diabetes.49.5.693

Localization of glucokinase gene expression in the rat brain. R M Lynch , L S Tompkins , H L Brooks , A A Dunn-Meynell and B E Levin Department of Physiology, University of Arizona, Arizona Health Sciences Center, Tucson 87524, USA. Abstract The brain contains a subpopulation of glucosensing neurons that alter their firing rate in response to elevated glucose concentrations. In pancreatic beta-cells, glucokinase (GK), the rate-limiting enzyme in glycolysis, mediates glucose-induced insulin release by regulating intracellular ATP production. A similar role for GK is proposed to underlie neuronal glucosensing. Via in situ hybridization, GK mRNA was localized to hypothalamic areas that are thought to contain relatively large populations of glucosensing neurons (the arcuate, ventromedial, dorsomedial, and paraventricular nuclei and the lateral area). GK also was found in brain areas without known glucosensing neurons (the lateral habenula, the bed nucleus stria terminalis, the inferior olive, the retrochiasmatic and medial preoptic areas, and the thalamic posterior paraventricular, interpeduncular, oculomotor, and anterior olfactory nuclei). Conversely, GK message was not found in the nucleus tractus solitarius, which contains glucosensing neurons, or in ependymal cells lining the third ventricle, where others have described its presence. In the arcuate nucleus, >75% of neuropeptide Y-positive neurons also expressed GK, and most GK+ neurons also expressed KIR6.2 (the pore-forming subunit of the ATP-sensitive K+ channel). The anatomic distribution of GK mRNA was confirmed in micropunch samples of hypothalamus via reverse transcription-polymerase chain reaction (RT-PCR). Nucleotide sequencing of the recovered PCR product indicated identity with nucleotides 1092-1411 (within exon 9 and 10) of hepatic and beta-cell GK. The specific anatomic localization of GK mRNA in hypothalamic areas known to contain glucosensing neurons and the coexpression of KIR6.2 and NPY in GK+ neurons support a role for GK as a primary determinant of glucosensing in neuropeptide neurons that integrate multiple signals relating to peripheral energy metabolism.