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This study was designed to examine the interaction of exogenous and endogenous steroids and mineralocorticoid receptors on the cochlea in the mouse model. We observed that exogenous steroids can activate and modulate cochlear responses to cochlea stimulation. We determined that not only mineralocorticoid receptors but also glucocorticoid receptors can affect cochlear responses to cochlea stimulation. Although endogenous steroids can directly activate and modulate cochlear responses to cochlea stimulation, exogenous steroids can also interact with their endogenous ligands. Moreover, the presence of mineralocorticoid and glucocorticoid receptors can affect cochlear responses to cochlea stimulation.
The environment surrounding the inner ear is rich in endocrine active substances. Many of these molecules are known to affect cochlear function. Using the mouse model, we examined the interaction of exogenous and endogenous steroids and mineralocorticoid receptors on the cochlea. We observed that exogenous and endogenous steroids can activate and modulate cochlear responses to cochlea stimulation. In addition, we determined that not only mineralocorticoid receptors but also glucocorticoid receptors can affect cochlear responses to cochlea stimulation. Although endogenous steroids can directly activate and modulate cochlear responses to cochlea stimulation, exogenous steroids can also interact with their endogenous ligands. Moreover, the presence of mineralocorticoid and glucocorticoid receptors can affect cochlear responses to cochlea stimulation.
A high-fidelity reverse transcription-quantitative real-time polymerase chain reaction (RT-qPCR) method was developed for simultaneous detection and quantification of MERS-CoV and the camel beta-CoV genus Gammacoronavirus A (BtCoV-GA1), and its application was validated using an in vitro cell culture model. The detection of MERS-CoV RNA was accomplished by a TaqMan-based real-time RT-PCR that targeted the viral N gene. The specificity of the assay was demonstrated by employing patient specimens. The in vitro MERS-CoV assay was able to detect MERS-CoV RNA from clinical specimens within 2 days of collection. The sensitivity and reproducibility of the assay were evaluated with RNA from cell culture supernatants. The detection limit of the assay was 10 copies of viral RNA per reaction, indicating the high sensitivity of the developed assay. MERS-CoV RNA was detected in the bronchoalveolar lavage (BAL) fluid of four patients and in oropharyngeal swabs of three patients. In addition, MERS-CoV RNA was detected in bronchoalveolar lavage and oropharyngeal swabs of several camels and another animal.
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