PSYCHOSINE

PSYCHOSINE is a lipid of Sphingolipids (SP) class. Psychosine is associated with abnormalities such as Globoid cell leukodystrophy, Demyelinating Diseases, Multiple Sclerosis, nervous system disorder and Lysosomal Storage Diseases. The involved functions are known as Ionization, Pathogenesis, Demyelination, 5-(carboxyamino)imidazole ribonucleotide mutase activity and Increased Sensitivy. Psychosine often locates in Body tissue, CNS - Brain (MMHCC), Autosome, Peripheral Nervous System and Nerve Tissue. The associated genes with PSYCHOSINE are GALC gene, NTRK1 gene, JUN gene, ALPP gene and Polylysine. The related lipids are Fatty Acids, fatty aldehyde, lysophosphatidic acid, Stearic acid and stearoyl chloride. The related experimental models are Mouse Model and Streptozotocin Diabetes.

Cross Reference

Introduction

To understand associated biological information of PSYCHOSINE, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.

What diseases are associated with PSYCHOSINE?

PSYCHOSINE is suspected in Globoid cell leukodystrophy, Enzyme Deficiency, Demyelinating Diseases, Multiple Sclerosis, nervous system disorder, Lysosomal Storage Diseases and other diseases in descending order of the highest number of associated sentences.

Related references are mostly published in these journals:

Disease Cross reference Weighted score Related literature
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Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with PSYCHOSINE

MeSH term MeSH ID Detail
Hemolysis D006461 131 associated lipids
Uterine Cervical Neoplasms D002583 10 associated lipids
Leukodystrophy, Metachromatic D007966 4 associated lipids
Leukodystrophy, Globoid Cell D007965 6 associated lipids
Nerve Degeneration D009410 53 associated lipids
Encephalomyelitis, Autoimmune, Experimental D004681 26 associated lipids
Gaucher Disease D005776 13 associated lipids
Optic Atrophy D009896 2 associated lipids
Total 8

PubChem Associated disorders and diseases

What pathways are associated with PSYCHOSINE

Lipid pathways are not clear in current pathway databases. We organized associated pathways with PSYCHOSINE through full-text articles, including metabolic pathways or pathways of biological mechanisms.

Related references are published most in these journals:

Pathway name Related literatures
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PubChem Biomolecular Interactions and Pathways

Link to PubChem Biomolecular Interactions and Pathways

What cellular locations are associated with PSYCHOSINE?

Related references are published most in these journals:

Location Cross reference Weighted score Related literatures
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What functions are associated with PSYCHOSINE?


Related references are published most in these journals:

Function Cross reference Weighted score Related literatures

What lipids are associated with PSYCHOSINE?

Related references are published most in these journals:

Lipid concept Cross reference Weighted score Related literatures
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What genes are associated with PSYCHOSINE?

Related references are published most in these journals:


Gene Cross reference Weighted score Related literatures

What common seen animal models are associated with PSYCHOSINE?

Mouse Model

Mouse Model are used in the study 'Psychosine accumulates in membrane microdomains in the brain of krabbe patients, disrupting the raft architecture.' (White AB et al., 2009).

Streptozotocin Diabetes

Streptozotocin Diabetes are used in the study 'Direct quantitation of psychosine from alkaline-treated lipid extracts with a semi-synthetic internal standard.' (Jiang X et al., 2009).

Related references are published most in these journals:

Model Cross reference Weighted score Related literatures
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NCBI Entrez Crosslinks

All references with PSYCHOSINE

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Authors Title Published Journal PubMed Link
Murugesan V et al. Glucosylsphingosine is a key biomarker of Gaucher disease. 2016 Am. J. Hematol. pmid:27441734
Dai M et al. Progression of Behavioral and CNS Deficits in a Viable Murine Model of Chronic Neuronopathic Gaucher Disease. 2016 PLoS ONE pmid:27598339
Gramlich PA et al. A peptide-linked recombinant glucocerebrosidase for targeted neuronal delivery: Design, production, and assessment. 2016 J. Biotechnol. pmid:26795355
Watanabe H et al. Psychosine-triggered endomitosis is modulated by membrane sphingolipids through regulation of phosphoinositide 4,5-bisphosphate production at the cleavage furrow. 2016 Mol. Biol. Cell pmid:27170180
Zhu H et al. Generation of a LacZ reporter transgenic mouse line for the stereological analysis of oligodendrocyte loss in galactosylceramidase deficiency. 2016 J. Neurosci. Res. pmid:27426866
Goddard-Borger ED et al. Glycosynthase mediated synthesis of psychosine. 2016 Carbohydr. Res. pmid:27721144
Avola R et al. Krabbe's leukodystrophy: Approaches and models in vitro. 2016 J. Neurosci. Res. pmid:27638610
Del Grosso A et al. Lithium improves cell viability in psychosine-treated MO3.13 human oligodendrocyte cell line via autophagy activation. 2016 J. Neurosci. Res. pmid:27638607
Carter RL et al. Can psychosine and galactocerebrosidase activity predict early-infantile Krabbe's disease presymptomatically? 2016 J. Neurosci. Res. pmid:27638594
Nogueira-Rodrigues J et al. Axonal pathology in Krabbe's disease: The cytoskeleton as an emerging therapeutic target. 2016 J. Neurosci. Res. pmid:27638589