56,58 Interestingly, nicotine has been shown to decrease DNMT1 mRNA expression in cortical

and hippocampal GABAergic neurons in mice – this decrease PHA-665752 price results in GAD67 promoter demethylation, and is inversely related to an upregulation of cortical GAD67 protein.59 This information is highly relevant, as SZ patients tend to smoke tobacco at a rate that is 2- to 4-fold higher than Inhibitors,research,lifescience,medical in the general population,60 and are possibly drawn to the nicotine content for its effects on the aforementioned pathway. Less information is available on BD; genomic imprinting has been suggested by statistical genetics, but molecular approaches have not yielded the imprinted disease genes.61 A recent study applied methylation-sensitive representational difference analysis (MS-RDA) to lymphoblastoid cells derived from twins discordant for BD.62 One detected gene, named peptidylprolyl isomerase Elike (PPIEL), was hypomethylated in BD-affected twins, while a region of the spermine synthase (SMS) gene was hypermethylated Inhibitors,research,lifescience,medical versus unaffected twins; it has yet to be determined if either of these regions are biologically and functionally significant. In combined studies of epigenetics and DNA sequence, some interesting developments have been observed. It has recently been

shown Inhibitors,research,lifescience,medical that rare G variants of a G/A polymorphism in the potassium chloride co-transporter 3 gene (SLC12A6) may represent risk factors for BD.63 Eventually, it was discovered that variants containing the G allele were methylated at the adjacent cytosine, and this accompanied a decrease in gene expression in human lymphocytes.64 This hints at a functional link between epigenetics and genetic variation, and the association with BD is believable, as SLC12A6 mutations underlie Inhibitors,research,lifescience,medical another psychiatric disorder, Andermann Inhibitors,research,lifescience,medical syndrome, which is an autosomal recessive motor-sensory neuropathy associated with developmental and neurodegenerative defects.65 It is interesting to note that BD provides a unique

opportunity to investigate epigenetic variation between two extreme forms of the same disease – depression and mania. A study design of this variety would unfortunately be limited to the use of peripheral blood, buccal epithelial cells, and fibroblasts as experimental tissues, but nonetheless, it would be incredibly interesting to determine the state Calpain of the epigenome during manic and depressive states, in the same individual when the same genetic and environmental impacts are present. Alzheimer’s disease AD is a neurodegenerative disorder and the most common form of dementia in the elderly; it is characterized by the accumulation of intracellular neurofibrillary tangles (NFT) and extracellular amyloid plaques in the brain.66 AD often presents with psychiatric symptoms such as memory loss, mood swings, and irritability that increase in severity as the disease progresses.