In vitro studies on renin release

BL Jensen, UG Friis, O Skøtt - Renal Disease: Techniques and Protocols, 2003 - Springer
BL Jensen, UG Friis, O Skøtt
Renal Disease: Techniques and Protocols, 2003Springer
Renin is an aspartyl peptidase that is synthesized, stored, and released from
juxtaglomerular (JG) granular cells in the lamina media of the afferent arteriole. Each
afferent arteriole contains 5–20 JG cells. Renin catalyzes the cleavage of angiotensin I (ANG
I) from renin substrate; angiotensin I is further converted to the physiologically active form
angiotensin II by angiotensin-converting enzyme (ACE). Angiotensin II (ANG II) is an
important vasoconstrictor, and it promotes release of aldosterone from the adrenal gland …
Abstract
Renin is an aspartyl peptidase that is synthesized, stored, and released from juxtaglomerular (JG) granular cells in the lamina media of the afferent arteriole. Each afferent arteriole contains 5–20 JG cells. Renin catalyzes the cleavage of angiotensin I (ANG I) from renin substrate; angiotensin I is further converted to the physiologically active form angiotensin II by angiotensin-converting enzyme (ACE). Angiotensin II (ANG II) is an important vasoconstrictor, and it promotes release of aldosterone from the adrenal gland. Thus, the renin-angiotensin-aldosterone system is important in the regulation of salt and water homeostasis and blood pressure. In keeping with its complex homeostatic roles, the regulation of renin secretion is under the control of a number of systemic factors. Release is stimulated by decreases in arterial pressure, increases in sympathetic nervous activity, and by a decrease in the tubular NaCl concentration at the macula densa (MD).
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