TY - JOUR
T1 - Primaquine-induced differential gene expression analysis in mice liver using DNA microarrays
AU - Noel, Sanjeev
AU - Sharma, Sharad
AU - Shanker, Rishi
AU - Rath, Srikanta Kumar
N1 - Funding Information:
We are grateful to Dr. C.M. Gupta, Director and Dr. Sudhir Srivastava, Head, Toxicology Division, Central Drug Research Institute, for their interest in this study. We sincerely express gratitude to Mr. Ashok Singh, Mr. Amit Kumar Mitra, Mr. Prabhat Singh, Dr. Neetu Singh and Miss Neeti Sagar for critically reviewing the manuscript. One of the authors (S.N.) is recipient of Senior Research Fellowship from Council of Scientific and Industrial Research (CSIR). This study was funded by CSIR network project CMM0018. This paper bears Central Drug Research Institute communication no. 7220.
Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.
PY - 2007/9/24
Y1 - 2007/9/24
N2 - Primaquine (PQ), a clinically important derivative of 8-aminoquinoline used against the hepatic stages (hypnozoites) of Plasmodium vivax and Plasmodium ovale, was studied to evaluate and compare between mRNA expression, and biochemical and histological parameters of hepatic stress in adult Swiss mice (Mus musculus). Following single oral dose of PQ (40 mg/kg, bw), alanine aminotransferase (ALT) and aspartate aminotransferase (AST) along with hematoxylin and eosin stained liver sections did not show any signs of hepatic stress at 6, 12 and 24 h except for ALT activity at 6 h. However, analysis at RNA transcript level revealed consistent and significant deregulation (p < 0.01 and two-fold) of 16 probes corresponding to important cellular processes such as protein transportation, transcription regulation, intracellular signaling, protein synthesis, hematopoiesis, cell adhesion and cell proliferation. Pathway analysis identified large number of affected genes corresponding to 40 Gene Ontology terms having a z score greater than 2. These results indicate that PQ at high doses may affect gene expression in liver and may produce undesirable outcomes if consumed for longer durations.
AB - Primaquine (PQ), a clinically important derivative of 8-aminoquinoline used against the hepatic stages (hypnozoites) of Plasmodium vivax and Plasmodium ovale, was studied to evaluate and compare between mRNA expression, and biochemical and histological parameters of hepatic stress in adult Swiss mice (Mus musculus). Following single oral dose of PQ (40 mg/kg, bw), alanine aminotransferase (ALT) and aspartate aminotransferase (AST) along with hematoxylin and eosin stained liver sections did not show any signs of hepatic stress at 6, 12 and 24 h except for ALT activity at 6 h. However, analysis at RNA transcript level revealed consistent and significant deregulation (p < 0.01 and two-fold) of 16 probes corresponding to important cellular processes such as protein transportation, transcription regulation, intracellular signaling, protein synthesis, hematopoiesis, cell adhesion and cell proliferation. Pathway analysis identified large number of affected genes corresponding to 40 Gene Ontology terms having a z score greater than 2. These results indicate that PQ at high doses may affect gene expression in liver and may produce undesirable outcomes if consumed for longer durations.
KW - 8-Aminoquinoline
KW - Differential gene expression
KW - Microarray
KW - Primaquine
KW - Toxicogenomics
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U2 - 10.1016/j.tox.2007.06.098
DO - 10.1016/j.tox.2007.06.098
M3 - Article
C2 - 17686563
AN - SCOPUS:34548035168
SN - 0300-483X
VL - 239
SP - 96
EP - 107
JO - Toxicology
JF - Toxicology
IS - 1-2
ER -