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R J Russo

Publications and source records attributed to R J Russo.

27 records · Page 2Linked to original sources

Potent quinoxaline-spaced phosphono alpha-amino acids of the AP-6 type as competitive NMDA antagonists: synthesis and biological evaluation.

A series of alpha-amino-3-(phosphonoalkyl)-2-quinoxalinepropanoic acids was synthesized and evaluated for NMDA receptor affinity using a [3H] CPP binding assay. Functional antagonism of the NMDA receptor complex was evaluated in vitro using a stimulated [3H]TCP binding assay and in vivo by employing an NMDA-induced seizure model. Some analogues also were evaluated in the [3H]-glycine binding assay. Several compounds of the AP-6 type show potent and selective NMDA antagonistic activity both in vitro and in vivo. In particular alpha-amino-7-chloro-3-(phosphonomethyl)-2-quinoxalinepropanoic acid (1) displayed an ED50 of 1.1 mg/kg ip in the NMDA lethality model. Noteworthy is alpha-amino-6,7-dichloro-3-(phosphonomethyl)-2-quinoxalinepropanoic++ + acid (3) with a unique dual activity, displaying in the NMDA receptor binding assay an IC50 of 3.4 nM and in the glycine binding assay an IC50 of 0.61 microM.

2-Amino-5-phosphonovalerate↗

Cell migration in the rat embryonic neocortex.

Three-dimensional reconstructions of the normal rat embryonic (E) neocortex on days E15, E17, E19, and E21, using Skandha (software designed by J. Prothero, University of Washington, Seattle), show that the neocortical ventricular zone shrinks rapidly in the medial direction during cortical morphogenesis. [3H]thymidine autoradiography indicates that the shrinkage of the ventricular zone occurs before neurons in lateral and ventrolateral parts of layers IV-II are generated. Consequently, most of these neurons originate 400-1000 microns medial to their settling sites in the cortical plate. Embryos killed at daily intervals up to E21 after a single injection of [3H]thymidine on either E17 or E18 revealed the presence of a prominent migratory path, the lateral cortical stream, used by neurons migrating to the lateral and ventrolateral cortical plate; neurons migrating to the dorsal cortical plate follow a direct radial path. Arrival times of neurons in the cortical plate depend on the migratory path and are proportional to the overall distance travelled. Neurons that migrate only radially arrive in the dorsal cortical plate in two days (shortest route). Neurons that migrate laterally arrive in the lateral cortical plate in 3 days (longer route) and in the ventrolateral cortical plate in 4 days (longest route). [3H]thymidine autoradiography also shows that cells generated in the neocortical ventricular zone migrate in the lateral cortical stream for 5 or more days and accumulate in a reservoir. Cells leave the reservoir to enter the piriform cortex and destinations (as yet undetermined) in the basal telencephalon. The lateral cortical stream is found wherever the neocortical primordium surrounds the basal ganglia and is absent behind the basal ganglia. A computer analysis of nuclear orientation in anterior and posterior parts of the intermediate zone in the dorsal neocortex between days E17 and E22 shows that horizontally oriented nuclei are more common anteriorly where many cells are migrating laterally than posteriorly where most cells are migrating radially.

Animals↗

Regulation of L-arabinose transport in Salmonella typhimurium LT2.

The inducible L-arabinose transport system was characterized in Salmonella typhimurium LT2. Only one L-arabinose transport system with a Km of 2 X 10(-4) M was identified. The results suggested that araE may be the only gene which codes for L-arabinose transport activity under the conditions tested. An araE-lac fusion strain was used to study the induction of the araE gene. No araE expression was detected when the L-arabinose concentration was lower than 1 mM. The expression of araE reached a maximum in the presence of 50 mM L-arabinose, and was significantly reduced in the presence of 50 mM L-arabinose, and was significantly reduced in the presence of D-glucose. Expression of the araBAD and araE genes was coordinately regulated. The concentration of L-arabinose that allowed maximum araBAD gene expression was 50-fold lower in an araE+ strain compared to an araE strain.

Arabinose↗

Sequence complexity of nuclear RNA from 2-acetylaminofluorene-induced rat hepatomas and host cirrhotic liver.

The sequence complexities of nuclear of RNAs from 2-acetylaminofluorene-induced rat hepatomas and host cirrhotic livers were compared in RNA-driven and host cirrhotic livers were compared in RNA-driven hybridization experiments using iodinated single-copy DNa as a probe. Normal liver nuclei RNA hybridized to 10.0 +/- 0.3+ (mean +/- S.D.) of the DNA, indicating an RNA sequence complexity of 3.8 x 10(8) nucleotides. Although nuclear RNAs from cirrhotic livers displayed a greater variation between animals, the mean values for percent DNA hybridized (9.5 +/- 2.0%) and RNA sequence complexity (3.6 x 10(8) nucleotides) for 5 cirrhotic livers examined did not differ significantly from normal. Analysis of nuclear RNAs from 10 tumors, 8 of which were classified as moderately to well differentiated histologically, revealed a level of hybridization (9.5 +/- 1.8%) and a mean value of RNA sequence complexity (3.6 x 10(8) nucleotides) that were almost identical with those for normal liver. Variation in the complexity amont tumors was slightly less than that among cirrhotic liver RNAs. These results suggest that while growth characteristics, biochemical properties, and physiology are known to vary between hepatomas and normal or cirrhotic liver tissue, there is no substantial or consistent difference in the RNA sequence complexity of chemically-induced hepatoma cells compared with normal or chemically-induced cirrhotic liver.

2-Acetylaminofluorene↗