mortality/aging
|
• fewer than expected mice are present at weaning
|
cardiovascular system
|
• mice exhibit media hyperplasia of small and medium vessels unlike wild-type mice
|
|
• compared with wild-type mice and Agtr1atm1Unc homozygotes
|
|
• Ang II-treated mice exhibit an almost completely blunted increase in mean arterial blood pressure (MAP) and heart rate with an increased time to normalization of MAP compared with similarly treated wild-type mice
• PE-treated mice exhibit a smaller increase in MAP compared with similarly treated wild-type mice
|
homeostasis/metabolism
|
• serum levels of Ang II are increased compared to in wild-type mice and Agtr1btm1Cof homozygotes
|
|
• angiotensin II (Ang II)-treated mice exhibit an almost completely blunted increase in mean arterial blood pressure (MAP) and heart rate with an increased time to normalization of MAP compared with similarly treated wild-type mice
|
|
• phenylephrine (PE)-treated mice exhibit a smaller increase in MAP compared with similarly treated wild-type mice
• however, PE-treated mice exhibit a negative chronotropic response as in wild-type mice
|
renal/urinary system
|
• mice exhibit media hyperplasia of small and medium vessels unlike wild-type mice
|
kidney cyst
(
J:137944
)
|
• mice exhibit cystic dilated cavities unlike wild-type mice
|
|
• mice exhibit prominent renal mononuclear infiltrations with partially blastic appearance and a high rate of partial mitosis unlike wild-type mice
|
|
• severely dilated Bowman's space
|
|
• multifocal and focally extensive glomeruli atrophy
|
|
• partially dilated tubular lumina unlike in wild-type mice
|
growth/size/body
kidney cyst
(
J:137944
)
|
• mice exhibit cystic dilated cavities unlike wild-type mice
|
immune system
|
• mice exhibit prominent renal mononuclear infiltrations with partially blastic appearance and a high rate of partial mitosis unlike wild-type mice
|


Analysis Tools