Monoamine transport in theOctopus posterior salivary gland nerves

Summary Noradrenaline (NA) and 5-hydroxytryptamine (5-HT) accumulated on the proximal side of a ligature to the posterior salivary gland (PSG) nerves in the octopus PSG duct. The NA concentration continued to increase proximally up to 18 days after ligation when a level of 59 g/g was reached compared with 12 g/g distally and 16–18 g/g for the corresponding portions of the normal duct. The concentration of 5-HT after the same period was 8.5 g/g proximally and 0.7 g/g distally compared to 4–7 g/g for normal duct. Dopamine (DM) was undetectable either after ligation or in the non-ligated duct. Accumulations of dense-core synaptic vesicles were observed by electron microscopy in some of the axons on both sides of the ligature.The NA concentration in the gland shows a decrease 6–8 days post-ligation and by 16–18 days had fallen to 50% of the normal value. No change in the DM or 5-HT concentrations had occurred by this time. When the nerves had been ligated for 40 days the 5-HT level in the gland had also decreased but the DM concentration was comparable to control values. It is concluded that NA is the predominant aminergic neurotransmitter in the PSG nerves and that its transport from the brain to the gland is a continuous process.Ligating or cutting the PSG duct caused a decrease in diameter of the distal nerve bundles but many axons did not degenerate even after 40 days ligation. The continued existence of some of the axons may explain the slow depletion of monoamines from the gland. Morphological changes in the secretory cells of the glandular tubules were observed by light microscopy 40 days after interruption of the nerve supply. It is suggested that the PSG nerves are required for the maintenance of the glandular tubules.     

The effect of cyclic nucleotides on purine biosynthesis and the induction of PRPP synthetase during lymphocyte activation

The activation of lymphocytes has been used to study the regulation of mammalian gene expression. Concanavalin A (Con A) added to mouse spleen lymphocytes in serum-free medium leads to an increase in the rate of DNA synthesis as great as 1000 fold, commencing 20 hr after its addition. Prior to 20 hr, the rate of purine synthesis increases 10–100 fold as measured by accumulation of the purine intermediate, formyl glycineamide ribonucleotide (FGAR). Addition of dibutyryl cyclic GMP to the lymphocyte suspensions results in a 10 fold increase in the rate of DNA synthesis in the absence of Con A and enhances both purine synthesis and DNA synthesis in its presence. The activity of phosphoribosyl pyrophosphate synthetase (PRPP synthetase), an enzyme central to purine and pyrimidine biosynthesis, is increased 2–10 fold during the activation. The increase begins to appear 8 hr after Con A addition and requires concomitant protein synthesis. The induced PRPP synthetase activity is stimulated by the presence of cyclic GMP in the enzyme assay. Addition of dibutyryl cyclic AMP to Con A-stimulated lymphocytes inhibits FGAR production, the stimulation of DNA synthesis, and the appearance of cyclic GMP-sensitive PRPP synthetase. These studies suggest that cyclic nucleotides play a significant role in the molecular mechanism of lymphocyte activation, the regulation of purine biosynthesis, and of eucaryotic genetic expression.     

Selective esterification of 1,6-anhydrohexopyranoses: The possible role of intramolecular hydrogen-bonding

Selective esterification reactions of 1,6-anhydro-3-deoxy-β-D-xylo-hexopyranose(1), 1,6-anhydro-β-D-glucopyranose (7), and several derivatives of 7, were conducted with an acid chloride or acid anhydride in pyridine. Reaction of 1 with p-toluenesulfonyl chloride and with benzoyl chloride gave 70 and 63%, respectively, of the 2-esters. The 2-methyl and 2-benzyl ethers of 7, both having strongly hydrogen-bonded C-4 hydroxyl group, reacted with p-toluenesulfonyl chloride to yield the 4-monosulfonates (71 and 74%, respectively). Esterification of the 2-methyl ether and 2-p-toluenesulfonate of 7 with p-toluenesulfonic anhydride instead of with p-toluenesulfonyl chloride led to increased yields of the 4-p-toluenesulfonates after a shorter reaction-time.     

The isolation of pig liver monoamine oxidase

Monoamine oxidase from pig liver has been isolated and purified approximately three hundred-fold. This enzyme has a molecular weight of 1,200,000, is highly polymeric, and contains subunits of molecular weight 146,000, as determined by Sephadex chromatography. The apparent K_m at 25°C is 1.28 × 10^?6 M at pH 9.0 (0.05 M glycine) and 1.74 × 10^?5 M at pH 7.2 (0.2 M phosphate) using benzylamine as a substrate. This enzyme contains approximately 8 copper(II) ions per 1,200,000 molecular weight.     

ELECTRICAL AND MECHANICAL CHARACTERISTICS OF A VERY FAST LOBSTER MUSCLE

The remotor muscle of the second antenna of the American lobster is functionally divided into two parts. One part produces slow, powerful contractions and is used for postural control. The other part produces very brief twitches, can follow frequencies over 100/sec without fusion and is probably used for sound production. This great speed is due, in part, to synchronous arrival of nerve impulses at multiple terminals, a very brief membrane electrical response and electrical continuity throughout large volumes of sarcoplasm. Calculations indicate that the very extensive sarcoplasmic reticulum is probably responsible for the rapid decline of tension in this muscle.     

Photoreaction of manganese catalyst in photosynthetic oxygen evolution

The formation of active O₂ evolving centers following addition of Mn²⁺ to Mn deficient Anacystis nidulans cells yielded an estimate of 6 to 12 Mn atoms associated with each O₂ evolving reaction center. Restoration of activity upon addition of Mn ions is affected in 3 ways: (1) Stimulation of the uptake of exogenous Mn into the cells—this uptake occurs in darkness, but is enhanced 5 to 10 fold by light; a high concentration of DCMU (1 × 10⁻⁵m) decreases this light enhanced influx no more than 50 to 75%; (2) Photoreactivation of the O₂ evolving centers, after excess Mn has been accumulated in the cells essentially no increase in Hill activity is observed unless the cells are illuminated. This photoreactivation is fully inhibited by 10⁻⁶m DCMU and partially by benzoquinone. The Q₁₀ of photoreactivation proper is close to 1; (3) Photoinhibition of the activation—photoreactivation occurs most effectively in weak intensities (< one-fiftieth photosynthetic saturation in normal cells). Apparently at higher intensities an inhibitory photoprocess is overriding. This inhibition proved reversible. The photoreactivation leads to new stable O₂ evolving centers as evidenced by an increase in the rate at saturating intensity, quantum yield, and the O₂ gush.