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. 2006 Dec;11(4):309–324. doi: 10.1379/CSC-199.1

Fig 1.

Fig 1.

 Expression of AT1 angiotensin II receptor in cortex and medulla from NP, LP, and RP fed rats. RT-PCR for AT1 receptor cDNA (385-bp product) was performed on RNA isolated from cortex and medulla of kidney homogenates. Representative gels of AT1 mRNA in cortex and medulla from controls (NP), LP, and RP after readministration of 24% protein for 14, 21, and 30 days are shown. Amplification of corresponding β-actin mRNA is shown. These results are typical of 5 independent observations. Semiquantitative PCR analysis of AT1 angiotensin II receptor. Top, Densitometric analysis of AT1 angiotensin II receptor and β-actin showed increased AT1 receptor/β-actin mRNA ratio in LP cortex related to NP cortex kidneys (**P < 0.01). Increased AT1 receptor/β-actin mRNA ratio incortex from RP after 14 days was shown, related to NP 14 days, (*P < 0.05). Bottom, Densitometric analysis. LP medulla related to NP medulla kidneys (*P < 0.05). Persistent increased AT1 receptor/β-actin mRNA ratio in medulla from RP after 14 days was shown, related to NP 14 days, (*P < 0.05). Values are means ± SEM