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Background/Objectives:: Antibiotics are commonly prescribed for children. Use of antibiotics early in life has been linked to weight gain but there are no large-scale, population-based, longitudinal studies of the full age range among mainly healthy children. Subjects/Methods:: We used electronic health record data on 163?820 children aged 3–18 years and mixed effects linear regression to model associations of antibiotic orders with growth curve trajectories of annual body mass index (BMI) controlling for confounders. Models evaluated three kinds of antibiotic associations—reversible (time-varying indicator for an order in year before each BMI), persistent (time-varying cumulative orders up to BMIj) and progressive (cumulative orders up to prior BMI (BMIj-1))—and whether these varied by age. Results:: Among 142?824 children under care in the prior year, a reversible association was observed and this short-term BMI gain was modified by age (P<0.001); effect size peaked in mid-teen years. A persistent association was observed and this association was stronger with increasing age (P<0.001). The addition of the progressive association among children with at least three BMIs (n=79?752) revealed that higher cumulative orders were associated with progressive weight gain; this did not vary by age. Among children with an antibiotic order in the prior year and at least seven lifetime orders, antibiotics (all classes combined) were associated with an average weight gain of approximately 1.4?kg at age 15 years. When antibiotic classes were evaluated separately, the largest weight gain at 15 years was associated with macrolide use. Conclusions:: We found evidence of reversible, persistent and progressive effects of antibiotic use on BMI trajectories, with different effects by age, among mainly healthy children. The results suggest that antibiotic use may influence weight gain throughout childhood and not just during the earliest years as has been the primary focus of most prior studies.

To determine if long-term exposure to high levels of lead in the environment is associated with decrements in cognitive ability in older Americans.

A systematic study of the synthesis and characterization of 3,3′‐disulfonated‐4,4′‐dichlorodiphenyl sulfone (SDCDPS) monomer was conducted by varying reactant stoichiometries (molar ratios of 4,4′‐dichlorodiphenyl sulfone (DCDPS) to SO3 1 : 2.2, 1 : 2.9, and 1 : 3.3), reaction temperature (90–120°C), and reaction time (4–6 h). The optimum synthesis batch process variables were 1 : 3.3 reactant molar ratio (DCDPS : SO3) at 110°C for 6 h. In earlier studies, recrystallization of the “crude” disulfonated monomer from alcohol–water mixture was necessary to remove the monosulfonated and DCDPS impurities that lowered yield. However, in the current research, SDCDPS was successfully synthesized at nearly 100% conversion, which effectively eliminated the need for recrystallization. Recrystallization of SDCDPS from several alcohol–water mixtures (methanol–, ethanol–, and isoproponal–water mixtures) was investigated to compare product purities. Several characterization methods including proton NMR, HPLC, UV–visible, and fast atom bombardment mass spectroscopy confirmed that the crude SDCDPS was completely disulfonated and identical to recrystallized SDCDPS, without having any monosulfonated or starting material DCDPS impurities. Hence, it was demonstrated that the crude SDCDPS monomer by the current one‐step process and the recrystallized SDCDPS monomer were identical. This optimized monomer synthesis has been used to scale up the SDCDPS and poly(arylene ether sulfone) random and statistical copolymers at controlled disulfonation (35 and 45 mol %) levels, which were then used to fabricate proton exchange membranes for fuel cell applications. The intrinsic viscosity data confirmed that high molecular weight film forming copolymers were synthesized. The calculated degree of disulfonations by proton NMR was in close agreement with target disulfonations. It may be concluded that this optimized SDCDPS synthesis eliminates the need for recrystallization, which would be expected to improve process economics. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 4595–4602, 2006

A boronic acid-containing coumarin aldehyde was designed and synthesized. The sensor binds to catecholamines such as dopamine and norepinephrine by forming an iminium ion with the amine as well as a boronate ester with the catechol. An internal hydrogen bond produces a colorimetric response to these analytes with good selectivity for catecholamines over simple amines. The fluorescence of the sensor is quenched by the catechol.

We report the isolation and characterization of an endohedral metallofullerene encapsulating three lanthanide atoms inside a nanoscale C80 cage, Lu3N@C80. In addition, we also report encapsulated mixed-metal species of gadolinium/lutetium and holmium/lutetium, Lu3-xAxN@C80 (x = 0−2), which may prove useful as multifunctional contrast agents for X-ray, MRI, and radiopharmaceuticals.

A number of new aryl phosphorus-containing polymers were found to be miscible with the commercially significant bisphenol A-based poly(hydroxy ether)s (PHE) over the entire composition range by differential scanning calorimetry (DSC) and dynamic mechanical analysis (DMA) measurements of the blends. Both the FTIR and CP-MAS ³¹P NMR results suggested extensive hydrogen-bonding interactions between hydroxyl groups and the phosphonyl groups. Specifically, the poly(arylene thioether diphenylphenylphosphine oxide) and phosphorus-containing polyimides were also miscible with PHE, again emphasizing the importance of phosphonyl groups for generating miscible polymer blends. In contrast, a structurally similar commercial polyimide, Ultem, was not miscible with PHE. These results suggested that the miscibility was induced mainly by hydrogen bonding between phosphonyl and hydroxyl groups, rather than other sites such as carbonyl or ether oxygen atoms and the hydroxyl groups. Furthermore, the measurements of proton spin−lattice relaxation times in the rotating frame (T1ρ) showed that the phosphorus-containing polyimide/PHE blends were homogeneous even at about a 4 nm scale.

This work describes the synthesis of two novel macrocyclic taxoid constructs by ring-closing olefin metathesis (RCM) and their biological evaluation. Computational studies examine conformational profiles of 1 and 2 for their fit to the β-tubulin binding site determined by electron crystallography. The results support the hypothesis that paclitaxel binds to microtubules in a “T” conformation.

The isomeric diamine monomer 5(6)-amino-1-(4-aminophenyl)-1,3,3-trimethylindane (DAPI) was successfully synthesized via the dimerization of α-methylstyrene followed by nitration and reduction. High molecular weight, soluble polyimides were synthesized via ester–acid solution imidization techniques and had glass-transition temperature values ranging from 247 to 369 °C. The polymers were soluble in common organic solvents because of the asymmetric and nonplanar nature of DAPI and displayed good short-term thermal stability by thermogravimetric analysis, as shown by their 5% weight-loss values above 500 °C in air. The DAPI/(3,4-dicarboxyphenyl) hexafluoropropane dianhydride (6FDA) polyimide also showed 2-h thermal stability at 400 °C under nitrogen, despite the partial aliphatic character. Refractive index values as low as 1.571 were observed for DAPI/6FDA, which allows an estimated dielectric constant of 2.47 to be derived. The permeation of O2 and N2 was conducted on thin dense films. The bulky, bent, and isomeric nature of DAPI imparted film-forming membranes that permitted high O2 permeability. In combination with 3,3',4,4'-benzophenone tetracarboxylic dianhydride (BTDA), DAPI had a good combination of O2 permeability and O2/N2 selectivity values of 2.8 Ba and 7.3, respectively. The polymerization method utilized to facilitate the cyclization of DAPI/BTDA to the polyimide affected the final thermal properties of the resulting polymer. The chemical imidization of DAPI/BTDA generated a polyimide with a glass-transition temperature value of 311 °C and a 5% weight-loss value in air of 457 °C. However, thermal and ester–acid imidization routes yielded an increase in the thermal properties. The ester–acid solution imidization of DAPI/BTDA produced a polymer glass-transition temperature value of 333 °C and a 5% weight-loss value of 525 °C in air. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 2840–2854, 2000

This paper reports the composition and properties of a new family of thermoplastics based on poly(hydroxyamino ether). The first commercial grades have been designed for applications in the adhesive and barrier resin markets. These polymers offer a unique set of properties, including excellent adhesion to a variety of substrates, high resistance to gas permeation, superior clarity, and good mechanical strength and toughness. In addition, they are amorphous and can be easily processed using conventional thermoplastic processing techniques. Some commercial applications of poly(hydroxyamino ether) resins include barrier packaging, starch based foam packaging, and powder coatings.

Ras activation occurs through stimulation of an upstream growth factor receptor such as epidermal growth factor receptor (EGFR). The ultimate effect of Ras is to induce nuclear transcription via a signaling pathway sequentially involving Raf, MAP kinase kinase (MEK), and mitogen-activated protein kinase (MAPK). To transform cells, Ras oncoproteins must be posttranslationally modified with a farnesyl group in a reaction catalyzed by farnesyl protein transferase. Farnesyltransferase inhibitors, therefore, have been proposed as potent anticancer agents. This study demonstrates the growth-inhibitory effects of farnesyltransferase inhibitor SCH66336 on human glioblastoma cell lines U-251 MG, U-251/E4 MG (a stably transfected cell line with elevated EGFR expression), and U-87 MG. As determined by (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl-2-(4-sulfophenyl)-2H-tetrazolium, inner salt) (MTS) and viability assays, the concentration required to achieve 50% inhibition (IC50) ranged from 30 microM (single 24-h treatment) to 10 microM (5-day treatment). U-251/E4 MG with overexpression of EGFR were more sensitive than U-251 MG parental cells. These observations were also supported by soft agar analysis. Cells treated with SCH66336 underwent G2 arrest. Western blot analysis revealed a decrease in phospho-MAPK levels upon treatment with 10 microM SCH66336, whereas MAPK levels were unaffected by the drug. Interestingly, increased expression of EGFR was observed in U-251 MG and U-251/E4 MG but not in U-87 MG in the presence of the inhibitor. These results demonstrate that SCH66336 inhibits viability and anchorage-independent growth in a time- and dose-dependent manner in glioblastoma cell lines U-251 MG, U-251/E4 MG, and U-87 MG via a signal transduction pathway involving the down-regulation of phospho-MAPK. Overexpression of EGFR appears to alter cellular sensitivity to farnesyltransferase inhibitors. This may have a particularly important implication in glioblastoma, where over 50% of tumors have amplification and overexpression of EGFR.

A methanol extract of Combretum erythrophyllum showed inhibitory bioactivities in a yeast-based microtiter assay for DNA-damaging agents. Bioassay-guided fractionation of this extract yielded two known bioactive compounds, combretastatin A-1 and (−)-combretastatin, and two new bioactive glucosides, combretastatin A-1 2‘-β-d-glucoside (1) and combretastatin B-1 2‘-β-d-glucoside (2). The structures of the new compounds were assigned by ¹H and ¹³C NMR, DEPT, HMQC, and HMBC spectra.

OBJECTIVES: To examine any association between social, productive, and physical activity and 13 year survival in older people. DESIGN: Prospective cohort study with annual mortality follow up. Activity and other measures were assessed by structured interviews at baseline in the participants' homes. Proportional hazards models were used to model survival from time of initial interview. SETTING: City of New Haven, Connecticut, United States. PARTICIPANTS: 2761 men and women from a random population sample of 2812 people aged 65 and older. MAIN OUTCOME MEASURE: Mortality from all causes during 13 years of follow up. RESULTS: All three types of activity were independently associated with survival after age, sex, race/ethnicity, marital status, income, body mass index, smoking, functional disability, and history of cancer, diabetes, stroke, and myocardial infarction were controlled for. CONCLUSIONS: Social and productive activities that involve little or no enhancement of fitness lower the risk of all cause mortality as much as fitness activities do. This suggests that in addition to increased cardiopulmonary fitness, activity may confer survival benefits through psychosocial pathways. Social and productive activities that require less physical exertion may complement exercise programmes and may constitute alternative interventions for frail elderly people.

The preservation of tropical rainforests is an important goal both for the intrinsic value of their cultural and biological diversity as well as for the well-being of the peoples who make these forests their home. In addition, tropical forests are potential sources of new pharmaceutical products that can only be found by chemical prospecting in Nature's genetically encoded combinatorial library. As part of an effort to integrate biodiversity conservation and drug discovery with economic development, we have initiated a collaborative program to discover potential pharmaceuticals in the rainforest of Suriname. The plant Renealmia alpinia (Zingiberaceae) was selected for investigation based on its ethnomedical use as a febrifuge, but testing in the yeast Sc-7 assay gave a positive response, indicative of cytotoxic activity. Using this bioassay, the two new labdane diterpenes, 11-hydroxy-8(17),12(E)-labdadien-15,16-dial 11,15-hemiacetal (1) and 16-oxo-8(17),12(E)-labdadien-15-oic acid (2), and the known diterpene, 8(17),12(E)-labdadien-15,16-dial (3), have been isolated. Their structures were elucidated by 1D and 2D NMR techniques (DEPT, COSY, HETCOR, HMBC, and NOESY) and IR, UV, and MS spectra, and the absolute stereochemistry of 1 was established by CD spectroscopy and by the formation and NMR analysis of α-methoxyphenylacetyl esters. The hemiacetal 1 was cytotoxic to M109 cells, with an IC50 value of 2.6 μg/mL.

Poly(urethane/crown ether rotaxane)s 7c−g were prepared from bis(p-tert-butylphenyl)bis[p-(2-(2‘-hydroxyethoxy)ethoxy)phenyl]methane (diol BG 4), tetrakis(ethylene glycol) (5) and 4,4‘-methylenebis(phenyl isocyanate) (MDI) (6) using 30-crown-10 (30C10) as solvent. It was found that threading efficiencies (m/n value, average number of cyclics per repeat unit) of 7c−g increased with the feed proportion of diol BG 4. Compared to poly(ester rotaxane)s in which the crown ethers can freely move along the backbone, the dethreading rate during polymerization is slow due to the H-bonds between in-chain NH groups and threaded crown ethers. In poly(urethane rotaxane)s, crown ethers are localized at the NH sites by H-bonding in chloroform, locked translationally and perhaps rotationally, to afford a well-defined microstructure. However, the cyclics tend to be in the vicinity of BG units in DMSO, which disrupts the H-bonding. Induction of shuttling between the two sites is caused by the use of mixtures of DMSO and CHCl3. Therefore, 7c−g are considered to be the first polymeric molecular switches reported so far. Threaded 30C10 has much shorter relaxation time than its free counterpart; this is a novel and easy method to characterize the formation of polyrotaxanes. The glass transition temperatures of 7c−g increase with the amount of BG units in the polymers, an easy approach to adjust Tg's of polyurethanes.

Guanosine 5'-diphosphate 3'-diphosphate (ppGpp) and guanosine 5'-triphosphate 3'-diphosphate (pppGpp) were detected in formic acid extracts of air-exposed culutres of Bacteroides thetaiotaomicron. The identification of ppGpp and pppGpp in B. thetaiotaomicron was based on the following results: (i) cochromatography of 32P-labeled hyperphosphorylated nucleotides in two different two-dimensional solvent systems with authentic ppGpp and pppGpp; (ii) incorporation of [3H]guanosine into the putative ppGpp and pppGpp; (iii) alkaline lability; and (iv) resistance, to periodate oxidation. There was a marked increase in the concentration of ppGpp and pppGpp after shift from anaerobic to aerobic conditions, and accumulation of both ppGpp and pppGpp was blocked under these conditions by pretreatment of the culture with rifampin or tetracycline. Growth and incorporation of [3H]guanosine, [3H]tymidine, [14C]succinate, and L-[35S]methionine into macromolecules were inhibited immediately upon exposure to air. The accumulation of ppGpp and pppGpp in B. thetaiotaomicron upon exposure to air may represent a novel signal for synthesis of these compounds.

Extracts of Ruminococcus albus were not able to convert pyruvate to acetyl phosphate, CO2, and H2 after passage through a diethylaminoethyl (DEAE)-cellulose column. Activity was restored by a brown protein fraction eluted from the column with 0.4 M Cl-. The protein was partially purified and shown to have the spectral and biological characteristics of ferredoxin. R. albus ferredoxin, Clostridium pasteurianum ferredoxin, and methyl viologen restored activity for pyruvate decomposition by DEAE-cellulose-treated R. albus extracts. R. albus or C. pasteurianum ferredoxin restored the ability of DEAE-cellulose-treated C. pasteurianum extracts to form H2 and acetyl phosphate from pyruvate. Ferredoxin-free extracts of R. albus reduced nicotinamide adenine dinucleotide (NAD) when supplemented with R. albus or C. pasteurianum ferredoxin or with methyl viologen. These extracts reduced NADP with H2 poorly unless both ferredoxin and NAD were added, which indicates the presence of an NADH:NADP transhydrogenase. Flavin mononucleotide and flavin adenine dinucleotide were rapidly reduced by H2 by ferredoxin-free extracts in the absence of ferredoxin.

The solution polycondensation of 1-(4-aminophenyl)-5(6)-aminoindane (DAPI) with a number of commercially available dianhydrides using the two-step ester-acid solution imidization route is described. High molecular weight polyimides were successfully synthesized from a 1:1 molar ratio of dianhydride to diamine. These film-forming systems have high glass transition temperatures (331–368 °C) and very good short-term thermal stability as judged by differential scanning calorimetry (DSC) and thermal gravimetric analysis (TGA). The fully cyclized polyimides are also highly soluble in common solvents.

Cerebral blood flow PET scans and high-density event-related potentials (ERPs) were recorded (separate sessions) while subjects viewed rapidly-presented, lower-visual-field, bilateral stimuli. Active attention to a designated side of the stimuli (relative to passive-viewing conditions) resulted in an enhanced ERP positivity (P1 effect) from 80–150 msec over occipital scalp areas contralateral to the direction of attention. In PET scans, active attention vs. passive showed strong activation in the contralateral dorsal occipital cortex, thus following the retinotopic organization of the early extrastriate visual sensory areas, with some weaker activation in the contralateral fusiform. Dipole modeling seeded by the dorsal occipital PET foci yielded an excellent fit for the P1 attention effect. In contrast, dipoles constrained to the fusiform foci fit the P1 effect poorly, and, when the location constraints were released, moved upward to the dorsal occipital locations during iterative dipole fitting. These results argue that the early ERP P1 attention effects for lower-visual-field stimuli arise mainly from these dorsal occipital areas and thus also follow the retinotopic organization of the visual sensory input pathways. These combined PET/ERP data therefore provide strong evidence that sustained visual spatial attention results in a preset, top-down biasing of the early sensory input channels in a retinotopically organized way. Hum. Brain Mapping 5:280–286, 1997. © 1997 Wiley-Liss, Inc.

High molecular weight poly(dimethylsiloxane)/semicrystalline cycloaliphatic polyester segmented copolymers based on dimethyl-1,4-cyclohexane dicarboxylate were prepared and characterized. The copolymers were synthesized using a high trans content isomer that afforded semicrystalline morphologies. Aminopropyl-terminated poly(dimethylsiloxane) (PDMS) oligomers of controlled molecular weight were synthesized, end capped with excess diester to form a diester-terminated oligomer, and incorporated via melt transesterification step reaction copolymerization. The molecular weight of the polysiloxane and chemical composition of the copolymer were systematically varied. The polysiloxane segment was efficiently incorporated into the copolymers via an amide link and its structure was unaffected by low concentrations of titanate transesterification catalyst, as shown by control melt experiments. The homopolymer and copolymers were characterized by solution, thermal, mechanical, and surface techniques. The segmented copolymers were microphase separated as determined by differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), and by transmission electron microscopy (TEM). It was demonstrated that relatively short poly(dimethylsiloxane) segment lengths and compositions were required to maintain single phase melt polymerization conditions. This was, in fact, the key to the successful preparation of these materials. The copolymers derived from short poly(dimethylsiloxane) segments demonstrated good mechanical properties, melt viscosities representative of single phase polymer melts, and were easily compression molded into films. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 3495–3506, 1997

A computed tomographic atlas of the dog brain has been produced. It should be helpful in determining the anatomical localization of lesions in canine models.

Cerebral blood flow PET scans and high‐density event‐related potentials (ERPs) were recorded (separate sessions) while subjects viewed rapidly‐presented, lower‐visual‐field, bilateral stimuli. Active attention to a designated side of the stimuli (relative to passive‐viewing conditions) resulted in an enhanced ERP positivity (P1 effect) from 80–150 msec over occipital scalp areas contralateral to the direction of attention. In PET scans, active attention vs. passive showed strong activation in the contralateral dorsal occipital cortex, thus following the retinotopic organization of the early extrastriate visual sensory areas, with some weaker activation in the contralateral fusiform. Dipole modeling seeded by the dorsal occipital PET foci yielded an excellent fit for the P1 attention effect. In contrast, dipoles constrained to the fusiform foci fit the P1 effect poorly, and, when the location constraints were released, moved upward to the dorsal occipital locations during iterative dipole fitting. These results argue that the early ERP P1 attention effects for lower‐visual‐field stimuli arise mainly from these dorsal occipital areas and thus also follow the retinotopic organization of the visual sensory input pathways. These combined PET/ERP data therefore provide strong evidence that sustained visual spatial attention results in a preset, top‐down biasing of the early sensory input channels in a retinotopically organized way. Hum. Brain Mapping 5:280–286, 1997.© 1997 Wiley‐Liss, Inc.

A novel strategy to completely eliminate dethreading of captured cyclics during the preparation of polyrotaxanes has been developed. A new difunctional blocking group (BG), namely bis(p-tert-butylphenyl)bis[p-((5-(chlorocarbonyl)pentyl)oxy)phenyl]methane (diacid chloride BG 14), was prepared in an overall yield of 63% by a three-step method. BG 14 polymerized with bis[p-((2-hydroxyethoxy)ethoxy)phenyl]bis(p-tert-butylphenyl)methane (diol BG 15) using 30-crown-10 (30C10) as solvent to afford poly(ester rotaxane)s 17 with unique architectures having two BGs per repeat unit. The formation of the polyrotaxanes was proved by a chemical shift of threaded 30C10 different from that of unthreaded species, hydrolytic recovery of 30C10, and a 2D NOESY study and supported by the GPC analysis. It was found that the resulting polyrotaxanes 17 had threading efficiencies (m/n values, average number of cyclic molecules per repeat unit) 2 times as high as those of poly(ester rotaxane)s 16 made under the same conditions from diol BG 15 and sebacoyl chloride. By optimizing the conditions, the threading efficiency was increased to 0.172 in polyrotaxane 17c, almost 14 times as high as that (0.012) of the polyrotaxane of type 1 made from decanediol and sebacoyl chloride.

Glucose uptake by Bacteroides succinogenes S85 was measured under conditions that maintained anaerobiosis and osmotic stability. Uptake was inhibited by compounds which interfere with electron transport systems, maintenance of proton or metal ion gradients, or ATP synthesis. The most potent inhibitors were proton and metal ionophores. Oxygen strongly inhibited glucose uptake. Na+ and Li+, but not K+, stimulated glucose uptake. A variety of sugars, including alpha-methylglucoside, did not inhibit glucose uptake. Only cellobiose and 2-deoxy-D-glucose were inhibitory, but neither behaved as a competitive inhibitor. Metabolism of both sugars appeared to be responsible for the inhibition. Cells grown in cellobiose medium transported glucose at one-half the rate of glucose-grown cells. Spheroplasts transported glucose as well as whole cells, indicating glucose uptake is not dependent on a periplasmic glucose-binding protein. Differences in glucose uptake patterns were detected in cells harvested during the transition from the lag to the log phase of growth compared with cells obtained during the log phase. These differences were not due to different mechanisms for glucose uptake in the cell types. Based on the results of this study, B. succinogenes contains a highly specific, active transport system for glucose. Evidence of a phosphoenolpyruvate-glucose phosphotransferase system was not found.

An oxidized nicotinamide adenine dinucleotide phosphate/oxidized nicotinamide adenine dinucleotide (NADP+/NAD+) nonspecific L-glutamate dehydrogenase from Bacteroides thetaiotaomicron was purified 40-fold (NADP+ or NAD+ activity) over crude cell extract by heat treatment, (NH4)2SO2 fractionation, diethylaminoethyl-cellulose, Bio-Gel A 1.5m, and hydroxylapatite chromatography. Both NADP+- and NAD+-dependent activities coeluted from all chromatographic treatments. Moreover, a constant ratio of NADP+/NAD+ specific activities was demonstrated at each purification step. Both activities also comigrated in 6% nondenaturing polyacrylamide gels. Affinity chromatography of the 40-fold-purified enzyme using Procion RED HE-3B gave a preparation containing both NADP+- and NAD+-linked activities which showed a single protein band of 48,5000 molecular weight after sodium dodecyl sulfate-polyacrylamide gradient gel electrophoresis. The dual pyridine nucleotide nature of the enzyme was most readily apparent in the oxidative direction. Reductively, the enzyme was 30-fold more active with reduced NADP than with reduced NAD. Nonlinear concave 1/V versus 1/S plots were observed for reduced NADP and NH4Cl. Salts (0.1 M) stimulated the NADP+-linked reaction, inhibited the NAD+-linked reaction, and had little effect on the reduced NADP-dependent reaction. The stimulatory effect of salts (NADP+) was nonspecific, regardless of the anion or cation, whereas the degree of NAD+-linked inhibition decreased in the order to I- greater than Br- greater than Cl- greater than F-. Both NADP+ and NAD+ glutamate dehydrogenase activities were also detected in cell extracts from representative strains of other bacteroides deoxyribonucleic acid homology groups.

In the pursuit of naphthalene-based calixarenes, a Friedel−Crafts alkylation with unusual regiochemistry was observed. Treatment of carbinol 14 with catalytic triflic acid was expected to produce calixarenes of the class represented by 16. Instead, the major product was cyclic trimer 15, in which alkylation of each naphthalene ring occurred at the electronically deactivated position. The structure of compound 15 was assigned by 2-D NMR studies.

Cyst-like radiolucencies (“holes”) in ribs can be a manifestation of many different abnormalities. Two cases of child-abuse are presented in which the initial clue leading to the diagnosis of a battered-child was a cyst-like lytic lesion in the posterior rib cage.