scholarly journals Role of fractalkine–CX3CR1 pathway in seizure-induced microglial activation, neurodegeneration, and neuroblast production in the adult rat brain

2015 ◽  
Vol 74 ◽  
pp. 194-203 ◽  
Author(s):  
Idrish Ali ◽  
Deepti Chugh ◽  
Christine T. Ekdahl
2002 ◽  
Vol 81 (2) ◽  
pp. 257-269 ◽  
Author(s):  
G. Banisadr ◽  
F. Quéraud-Lesaux ◽  
M. C. Boutterin ◽  
D. Pélaprat ◽  
B. Zalc ◽  
...  

BioMetals ◽  
2008 ◽  
Vol 22 (2) ◽  
pp. 329-335 ◽  
Author(s):  
Charis Liapi ◽  
Apostolos Zarros ◽  
Stamatios Theocharis ◽  
Hussam Al-Humadi ◽  
Foteini Anifantaki ◽  
...  

2017 ◽  
Vol 92 ◽  
pp. 108-118 ◽  
Author(s):  
Hiroo Kaneta ◽  
Wataru Ukai ◽  
Hanako Tsujino ◽  
Kengo Furuse ◽  
Yoshiyasu Kigawa ◽  
...  

1978 ◽  
Vol 176 (3) ◽  
pp. 951-958 ◽  
Author(s):  
T B Patel ◽  
J B Clark

1. Data are provided that indicate that the rat brain acetoacetyl-CoA deacylase is almost exclusively mitochondrial. Developmental studies show that this enzyme more than doubles its activity during suckling (0–21 days) and then maintains this activity in adults (approx. 1.1 units/g wet wt.). 2. Kinetic studies (on the acetoacetyl-CoA deacylase) in a purified brain mitochondrial preparation give a Vmax. of 47 nmol/min per mg of protein, and a Km for acetoacetyl-CoA of 5.2 micron and are compatible with substrate inhibition by acetoacetyl-CoA above concentrations of 47 micron. 3. The total brain 3-hydroxy-3-methyl-glutaryl-CoA synthase remains constant in the developing and adult rat brain (approx. 1.2 units/g wet wt.). This enzyme is located in both the mitochondrial and cytosolic fractions. During suckling (0–21 days) the mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase represents approx. one-third of the total, but this increases markedly to about 60% of the total in the adult. The cytosolic enzyme correspondingly falls to approx. 40% of the total. 4. The role of the acetoacetyl-CoA deacylase in providing cytosolic acetoacetate for biosynthetic activities in the developing brain is discussed.


Toxicology ◽  
2005 ◽  
Vol 212 (2-3) ◽  
pp. 185-194 ◽  
Author(s):  
Lidia Strużyńska ◽  
Małgorzata Chalimoniuk ◽  
Grzegorz Sulkowski

2020 ◽  
Vol 21 (1) ◽  
Author(s):  
Karin Warfvinge ◽  
Diana Krause ◽  
Lars Edvinsson

Abstract Background Recent work, both clinical and experimental, suggests that the hypothalamic hormone oxytocin (OT) and its receptor (OTR) may be involved in migraine pathophysiology. In order to better understand possible central actions of OT in migraine/headache pathogenesis, we mapped the distribution of OT and OTR in nerve cells and fibers in rat brain with a focus on areas related to migraine attacks and/or shown previously to contain calcitonin gene related peptide (CGRP), another neuropeptide involved in migraine. Methods Distribution of OT and OTR in the adult, rat brain was qualitatively examined with immunohistochemistry using a series of well characterized specific antibodies. Results As expected, OT was extensively localized in the cell somas of two hypothalamic nuclei, the supraoptic (SO or SON) and paraventricular nuclei (Pa or PVN). OT also was found in many other regions of the brain where it was localized mainly in nerve fibers. In contrast, OTR staining in the brain was mainly observed in cell somas with very little expression in fibers. The most distinct OTR expression was found in the hippocampus, the pons and the substantia nigra. In some regions of the brain (e.g. the amygdala and the hypothalamus), both OT and OTR were expressed (match). Mismatch between the peptide and its receptor was primarily observed in the cerebral and cerebellar cortex (OT expression) and hippocampus (OTR expression). Conclusions We compared OT/OTR distribution in the CNS with that of CGRP and identified regions related to migraine. In particular, regions suggested as “migraine generators”, showed correspondence among the three mappings. These findings suggest central OT pathways may contribute to the role of the hypothalamus in migraine attacks.


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