Circulating natriuretic peptide hormones act to maintain homeostasis with regard to blood volume, blood pressure, and salt balance. When the myo-endocardial cells of the atrium sense an increase in blood volume or pressure, they release A- or B-type atrial natriuretic peptides (ANPs). These peptides, acting through guanylate cyclase receptors, dilate blood vessels and stimulate salt excretion by inhibiting sodium chloride reabsorption in the collecting ducts of the kidney. As the salt concentration within the ducts increases osmotic pressure, diuresis occurs. C-type natriuretic peptide, produced in the hypothalamus and pituitary, causes dilation in the circulatory system, including the heart, but has little effect on the kidney. Urodilatin is a paracrine natriuretic peptide, produced in the proximal tubules of the kidney, and acting in the collecting ducts. We offer all of these peptides, from several vertebrate sources, as well as some active peptide fragments. Atriopeptin II, for example, relaxes smooth muscle both in veins and in the gut. Dendroaspis natriuretic peptide, originally isolated from green mamba snake venom, is structurally similar to the A-,B-, and C-ANP′s, and exerts the same physiological functions.
Researchers will also find here several peptide hormones with effects on appetite and energy metabolism. Pancreatic polypeptide and derivatives work through neuropeptide Y receptors. Pancreastatin, which is elevated in diabetes, and the catecholamine release inhibitor catestatin are peptide hormones resulting from the enzymatic cleavage of chromagranin.
Atrial natriuretic peptide (ANP) is synthesized in myoendocrine cells of the heart from which it is released into the circulation. It exerts natriuretic, diuretic, and vasodilatory effects through stimulation of guanylate cyclase-linked NPR-A receptors. It plays an important role in blood volume and blood pressure homeostasis.
Atrial natriuretic peptide (ANP) is synthesized in myoendocrine cells of the heart from which it is released into the circulation. It exerts natriuretic, diuretic, and vasodilatory effects through stimulation of guanylate cyclase-linked NPR-A receptors. It plays an important role in blood volume and blood pressure homeostasis.
Atrial natriuretic peptide (ANP) is synthesized in myoendocrine cells of the heart from which it is released into the circulation. It exerts natriuretic, diuretic, and vasodilatory effects through stimulation of guanylate cyclase-linked NPR-A receptors. It plays an important role in blood volume and blood pressure homeostasis.
Brain natriuretic peptide (type B natriuretic peptide) was originally isolated from brain, but is mainly produced in myoendocrine cells of the heart ventricles from which it is released into the circulation. It is involved in blood pressure control and cardiovascular homeostasis.
Brain natriuretic peptide (type B natriuretic peptide) was originally isolated from brain, but is mainly produced in myoendocrine cells of the heart ventricles from which it is released into the circulation. It is involved in blood pressure control and cardiovascular homeostasis.
The catestatin peptide is produced from its precursor chromogranin A protein. Catestatin is a cationic and hydrophobic peptide that can stimulate histamine release from mast cells and exhibits potent catecholamine relase-inhibitory activity.
Structural homolog of natiuretic peptides containing a 17 amino acid disulfide ring similar to ANP, BNP, and CNP that mediate their physiological effects through particulate guanylyl cyclase receptors generating cGMP.
C-type natriuretic peptide is produced in the hypothalamus, anterior pituitary, and most major endocrine glands. It has potent venodilatory and coronary vasodilatory effects, but minimal effects on renal function.
Urodilatin is a natriuretic factor that is produced in the kidney and secreted into the urine. It regulates water and sodium reabsorption in the collecting duct.