PART IRenal Hypertension In an earlier study it was found that the renal artery of necropsied hypertensive subjects contained abnormally large amounts of sodium and water (1). The present study deals with the electrolyte composition of the aorta in rats with renal hypertension. After these aortas have been stripped of adventitia, at least two-fifths of the total area in tissue sections is occupied by smooth muscle cells. The remainder is largely connective tissue. The rat aorta thus provides for analysis a tissue rich in arterial smooth muscle. Moreover, the smooth muscle cells in the aorta are continuous with and have many of the pharmacological reactions of similar cells in the smaller arteries and arterioles (2). It seemed likely that any chemical alteration occurring in the aorta would give a clue to similar changes in the smooth muscle of arterioles. Technical difficulties have so far prevented us from analyzing the electrolyte content in the walls of arterioles.
METHODSHypertension was produced by compressing one kidney of 250 gm. male rats with a figure-of-eight ligature and removing the other kidney six days later. All the rats were fed rat chow 3 (.3 per cent sodium and 1.2 per cent potassium) and water ad lib. Eight weeks or longer after the second operation, blood pressure was determined and the rats were sacrificed for tissue analysis.The aortas were dissected, stripped of adventitia, blotted free of blood, and placed in weighing bottles. In one series of rats, tissues were dried, defatted, and extracted with 0.75N HNO, according to the method of Lowry and Hastings (3). Sodium and potassium concentrations 1 This investigation was supported by a grant-in-aid from The American Heart Association.2This work was done during the tenure of an Established Investigatorship of the American Heart Association. 3 Obtained from Uncle Johnny Mills, Houston, Texas.in the extract were determined with a Weichselbaum flame photometer. Chloride was determined by the potentiometric method of Kolthoff and Kuroda (4). In using this method, standard chloride solutions were used to bracket the unknown solutions. In another series of rats the tissues were dried and defatted as above, and extracted with 10 per cent trichloroacetic acid. Magnesium concentration was determined in this extract using the titan yellow method of Kunkel, Pearson, and Schweigert (5). Polyvinyl alcohol (Elvanol 51-05) was used to prevent precipitation of the MgOH-titan yellow complex.Sera were analyzed for water, sodium, and potassium by the same methods. Blood urea was determined by a standard urease-nesslerization method.Mean blood pressures were determined under ether anesthesia by direct puncture of the abdominal aorta below the level of the renal arteries. It was found that the depth of ether anesthesia could be varied considerably without changing the mean blood pressure. When the breathing of the rat indicated the proper plane of anesthesia, the blood pressure was read on the mercury manometer. This method gives very consistent results on normal...