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Nerve ending particles isolated from prenatal and postnatal rats by means of density-gradient centrifugation in a ficoll medium actively incorporated [32P]-orthophosphate into nucleotides, phosphoproteins and phospholipids. This process requires Mg2+; is dependent on malate plus pyruvate but not glucose, and is inhibited by dinitrophenol, gramicidin, oligomycin, azide, p-chloromercuribenzoate, CaCl2 but not iodoacetate. It was concluded that the metabolic energy at the synapse is derived largely from the mitochondria of the synaptic complex rather than from its cytoplasm. Thin-layer chromatography and paper electrophoresis revealed that the metabolically active phospholipids, namely phosphatidic acid, phosphatidyl inositol and the polyphosphoinositides which were found to be tightly bound to the phosphoprotein fraction, contained more than 90% of the total radioactivity but constituted less than 9% of the total phospholipids. The highest phosphoprotein and phospholipid content of the nerve endings (expressed in μmoles P/mg nerve ending protein) as well as maximal 32P-incorporation occurred just prior to and continued into the stage when functional changes are formed. It is suggested that an increase in the amount of enzymatic activity coupled with an increase in the permeability of the synaptosomal membrane to inorganic phosphate and other metabolites could trigger the rapid morpho-biochemical and functional changes observed in rat brain during this period of development. A simple density-gradient withdrawing device for the isolation of the submitochondrial particles after density-gradient centrifugation of the conventional mitochondrial fraction was described.

Separation of simple saturated hydroxamic acids with a chain length of one to nine carbon atoms has been achieved by partition chromatography on paper. The relative merits of a number of solvents are discussed.

Serum proteins of pregnant rats were analyzed by paper electrophoresis following administration of the teratogenic disazo dyes trypan blue, Evans blue, Niagara blue 4B, Niagara sky blue 6B, Congo red, and Niagara blue 2B. Sera were obtained from blood taken by cardiac puncture just before dye injection, 48 hours after dye injection; and again at autopsy. All of the dyes tested caused a reduction in serum albumin and total protein concentration and an elevation in the concentration of beta or alpha-2 globulins at some time during pregnancy. The remaining serum fractions reacted variably to the dye treatment. In spite of the rather consistent results presented in this paper, and similar findings reported for other teratogens, there is no direct proof that altered serum proteins, per se, are causally related to the production of malformations.