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2010
DOI: 10.1677/jme-10-0026
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Testosterone-induced permanent changes of hepatic gene expression in female mice sustained during Plasmodium chabaudi malaria infection

Abstract: Testosterone has been previously shown to induce persistent susceptibility to Plasmodium chabaudi malaria in otherwise resistant female C57BL/6 mice. Here, we investigate as to whether this conversion coincides with permanent changes of hepatic gene expression profiles. Female mice aged 10-12 weeks were treated with testosterone for 3 weeks; then, testosterone treatment was discontinued for 12 weeks before challenging with 10 6 P. chabaudi-infected erythrocytes.Hepatic gene expression was examined after 12 wee… Show more

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Cited by 28 publications
(10 citation statements)
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“…Hyperprolactinemia Did Not Influence the Serum Levels of GH or TT. Since expression of these sex-specific hepatic genes is regulated by GH, and some of them are also affected by testosterone (Deli c et al, 2010;Knopf et al, 1983), we verified the influence of hyperprolactinemia on serum levels of GH and TT. In both male and female mice treated with pCAGGS-mPrl, the serum levels of GH were not significantly Fig.…”
Section: Resultsmentioning
confidence: 90%
“…Hyperprolactinemia Did Not Influence the Serum Levels of GH or TT. Since expression of these sex-specific hepatic genes is regulated by GH, and some of them are also affected by testosterone (Deli c et al, 2010;Knopf et al, 1983), we verified the influence of hyperprolactinemia on serum levels of GH and TT. In both male and female mice treated with pCAGGS-mPrl, the serum levels of GH were not significantly Fig.…”
Section: Resultsmentioning
confidence: 90%
“…The quantitative evaluation was performed with aqman7500 system software (Applied Biosystems, Foster, MA, USA). Expression of genes was normalized to that of 18S rRNA .…”
Section: Methodsmentioning
confidence: 99%
“…Quality and integrity of RNA were determined using the Agilent RNA 6000 Nano Kit on the Agilent 2100 Bioanalyzer (Agilent Technologies). RNA was quantified by measuring A 260nm on the ND-1000 spectrophotometer (NanoDrop Technologies) (Delic et al 2010). All RNA samples were treated with DNase (Applied Biosystems, Darmstadt, Germany) for at least 1 h and were then converted into cDNA using the reverse transcription kit following the manufacturer's protocol (Qiagen, Hilden, Germany).…”
Section: Quantitative Pcrmentioning
confidence: 99%