Rat APJ mRNA distribution has been investigated using numerous techniques including in situ hybridization histochemistry (ISHH), Northern blots and reverse transcriptase-polymerase chain reaction (RT-PCR), with the strongest signals apparent in the lung and heart and lower levels evident in the brain hypothalamus and

cerebroventricular region, pituitary gland, skeletal muscle, kidney, spinal cord, thyroid gland, adipose tissue, ovary and uterus [9], [17], [30] and [34]. Similarly, RT-PCR studies have shown widespread APJ mRNA expression in human tissues; high APJ expression was observed in human spleen, placenta, spinal cord and corpus callosum with lower levels present in the hypothalamus, http://www.selleckchem.com/products/ldn193189.html hippocampus, lung, intestine, and stomach [30]. In contrast, quantitative real-time polymerase chain reaction (qPCR) studies in adult mouse tissues have shown APJ mRNA to be present in the pituitary, heart, lung, ovary, and uterus, with low expression levels in samples of whole brain and individual regions [30] and [41]. Limited distribution studies of APJ protein Crenolanib have been carried out to date. In the rat brain APJ protein expression was identified using immunohistochemistry (IHC) in the frontal and piriform cortices, the PVN, the pyramidal CA2 and CA3 cell layer of the hippocampus, dentate gyrus, spinal cord and

cerebellum [9]. APJ immunoreactivity (APJ-ir) has also been shown in the SON and magnocellular vasopressin and oxytocin neurones of the pituitary [51] and in endothelial Selleck Erastin cells lining small intramyocardial, renal, pulmonary and adrenal vessels, small coronary arteries, large conduit vessels, and endocardial endothelial cells [21] and [24]. The regional localization and distribution of APJ led to further work clarifying the functions of this receptor. Thus high APJ expression in regions such as the heart and hypothalamic PVN and SON led to investigation of roles for APJ in the cardiovascular system and in the regulation of water balance and stress responses [8], [21], [27], [31] and [49]. Recent studies have employed apelin- and/or APJ-knockout (KO) mice

to further investigate the significance of the apelinergic system in cardiovascular function [19] and [25] and in fluid homeostasis [42] and [43]. APJ KO mice lack the hypotensive response to peripherally injected apelin that is seen in wild type littermates [19] and show a significant reduction in exercise capacity following exercise stress [8], suggesting roles for APJ in blood pressure regulation and cardiac function, respectively. Additionally APJ KO mice show abnormal water metabolism, manifested by a change in drinking behavior and in the ability to concentrate urine [42], and an altered response to the osmotic stress of salt loading [43] compared with wild type littermates, suggesting that APJ is an important regulator of mechanisms controlling fluid homeostasis.