scholarly journals Opioid sensitivity in mice selectively bred to consume or not consume methamphetamine

2012 ◽  
Vol 19 (3) ◽  
pp. 370-379 ◽  
Author(s):  
Emily C. Eastwood ◽  
Tamara J. Phillips
Keyword(s):  
2021 ◽  
Vol 35 (S1) ◽  
Author(s):  
Nicholas Burgraff ◽  
Nathan Baertsch ◽  
Nicholas Bush ◽  
Jan‐Marino Ramirez

2016 ◽  
Vol 18 (4) ◽  
pp. 373-383 ◽  

Contrary to popular belief, sex hormones act throughout the entire brain of both males and females via both genomic and nongenomic receptors. Many neural and behavioral functions are affected by estrogens, including mood, cognitive function, blood pressure regulation, motor coordination, pain, and opioid sensitivity. Subtle sex differences exist for many of these functions that are developmentally programmed by hormones and by not yet precisely defined genetic factors, including the mitochondrial genome. These sex differences, and responses to sex hormones in brain regions and upon functions not previously regarded as subject to such differences, indicate that we are entering a new era in our ability to understand and appreciate the diversity of gender-related behaviors and brain functions.


2021 ◽  
Vol 35 (S1) ◽  
Author(s):  
Elizabeth Jaeckel ◽  
Alberto Perez‐Medina ◽  
Yoani Herrera ◽  
Erwin Arias‐Hervert ◽  
William Birdsong

2001 ◽  
Vol 21 (4) ◽  
pp. 1334-1339 ◽  
Author(s):  
Kazutaka Ikeda ◽  
Toru Kobayashi ◽  
Tomio Ichikawa ◽  
Toshiro Kumanishi ◽  
Hiroaki Niki ◽  
...  

2000 ◽  
Vol 93 (6) ◽  
pp. 1565-1565
Author(s):  
Douglas G. Merrill ◽  
James C. Eisenach

2012 ◽  
Vol 19 (1) ◽  
pp. 55-62 ◽  
Author(s):  
D Nishizawa ◽  
K Fukuda ◽  
S Kasai ◽  
J Hasegawa ◽  
Y Aoki ◽  
...  

2009 ◽  
Vol 29 (1) ◽  
pp. 76-86 ◽  
Author(s):  
I. Chizhmakov ◽  
N. Mamenko ◽  
T. Volkova ◽  
I. Khasabova ◽  
D. A. Simone ◽  
...  

eLife ◽  
2020 ◽  
Vol 9 ◽  
Author(s):  
Eduardo Javier López Soto ◽  
Diane Lipscombe

Cell-specific alternative splicing modulates myriad cell functions and is disrupted in disease. The mechanisms governing alternative splicing are known for relatively few genes and typically focus on RNA splicing factors. In sensory neurons, cell-specific alternative splicing of the presynaptic CaV channel Cacna1b gene modulates opioid sensitivity. How this splicing is regulated is unknown. We find that cell and exon-specific DNA hypomethylation permits CTCF binding, the master regulator of mammalian chromatin structure, which, in turn, controls splicing in a DRG-derived cell line. In vivo, hypomethylation of an alternative exon specifically in nociceptors, likely permits CTCF binding and expression of CaV2.2 channel isoforms with increased opioid sensitivity in mice. Following nerve injury, exon methylation is increased, and splicing is disrupted. Our studies define the molecular mechanisms of cell-specific alternative splicing of a functionally validated exon in normal and disease states – and reveal a potential target for the treatment of chronic pain.


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