Hepatic cyclophorase activity in rats treated with 1,2,3,4-tetrahydro-β-naphtylamine (THNA)

Riassunto Gli omogenati di fegato dei ratti sacrificati dopo 4 h dalla somministrazione di-tetraidronaftilammina (30 mg pro kg per via intraperitoneale) presentano una aumentata capacità di ossidare alcuni composti del Ciclo di Krebs, in rapporto ai controlli. Viene avanzata l'ipotesi che l'intensa glicogenolisi epatica e muscolare e l'aumentata acetilazionein vivo dell'acido para-aminobenzoico provocate nel ratto dalla somministrazione di-tetraidronaftilammina, siano causate da un esaltato metabolismo intermedio ossidativo.     

The effects of vitamin A nutritional status on microsomal lipid peroxidation and α-tocopherol level in rat liver

Summary In vitamin A-deficient rats, liver glutathione peroxidase activity was decreased, -tocopherol content was strongly enhanced, but microsomal liquid peroxidation remained unchanged.     

‘Classical’ and ‘new’ diabetogens—comparison of their effects on isolated rat pancreatic islets in vitro

This study compares functional and morphological alterations caused by application of alloxan, streptozotocin, xanthine oxidase/hypoxanthine (generation of reactive oxygen species), or S-nitroso-N-acetyl-D,L-penicillamine (SNAP, liberation of nitric oxide) to isolated rat pancreatic islets in vitro. In perifusion experiments, membrane leakage—detected by non-stimulated insulin release—was found after application of all drugs, but showed a substance-specific time pattern. Twenty-four hours after application of the classical diabetogens (alloxan or streptozotocin), potassium chloride- and glucose-stimulated insulin secretion were markedly reduced, while a persistent reduction was observed neither after exposure to xanthine oxidase/hypoxanthine, nor to SNAP. Morphological analysis of the islets revealed that nearly all β-cells were destroyed following alloxan or streptozotocin treatment, while the majority of β-cells were configured regularly after application of xanthine oxidase/hypoxanthine or SNAP. Necrotic cells found after xanthine oxidase/hypoxanthine usually differed in morphology from those observed after application of the classical diabetogens. While the former cells were characterised by swollen nuclei, the latter had shrunken nuclei with irregular condensed chromatin. Apoptosis was found only following nitric oxide exposure. Due to these differences, it seems unlikely that alloxan, streptozotocin, xanthine oxidase/hypoxanthine, and nitric oxide have a common major feature in their toxic action. Received 16 September 1999; received after revision 15 November 1999; accepted 26 November 1999     

Action ofβ-(4-chlorophenyl-GABA) on uptake and metabolism of GABA in different subcellular fractions of rat brain

Summary -(4-chlorophenyl)-GABA, a GABA mimetic compound, acts as an inhibitor of GABA metabolism in both synaptosomal and extrasynaptosomal compartments. It has no significant action on GABA or Glu uptake by synaptosomes.     

Antagonism of chlorpromazine byβ-melanocyte stimulating hormone (β-MSH)

Résumé Une préparation hautement purifiée de l'hormone mélanophorétique-MSH inhibe les effets de la chlorpromazine au niveau de la moelle spinale.     

Effect of glucose and phloretin-2′-β-D-glucose (phloridzin) on in vitro fertilization of mouse ova

Summary The fertilization ratio of mouse ova in vitro decreased when glucose concentration in the medium was lowered. However, the addition of phloretin-2--D-glucose (phloridzin), known as a glucose uptake inhibitor, restored the fertilization ratio back to the control level. The glucose moiety of the phloridzin seemed to be responsible for this effect.     

The effect ofβ-aminopropionitrile (BAPN) on bacteria

Zusammenfassung Alle untersuchten Bakterien waren gegenüber BAPN entweder ganz unempfindlich oder zeigten nur eine unspezifische Wachstumsverminderung. Diese Bakterien scheinen zum Studium lathyrogenischer Substanzen ungeeignet. Die Annahme, dass BAPN auf Mucopolysacchariden wirkt, konnte durch diese Untersuchung nicht gestützt werden.

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This work was supported by Research Grant A-4002 from the National Institute of Arthritis and Metabolic Diseases, U.S. Public Health Service. We are also grateful to Abbott Laboratories, North Chicago (Illinois) for generous gifts of mono--aminopropionitrile (BAPN) fumarate.     

In vitro dopaminergic neuroprotective and in vivo antiparkinsonian-like effects of Δ3,2-hydroxybakuchiol isolated from Psoralea corylifolia (L.)

Cocktail recipes containing Psoralea corylifolia seeds (PCS) are used to empirically treat Parkinson disease. A PCS isolate Δ³,2-hydroxybakuchiol (BU) can inhibit dopamine uptake in dopamine transporter (DAT) transfected Chinese hamster ovary (CHO) cells, and dopamine reuptake blockade may provide an alternative approach for ameliorating parkinsonism. Here, we assessed the potential dopaminergic neuroprotective, and antiparkinsonian-like activity of BU. BU sample size was increased by using a scale-up extraction paradigm. Pharmacologically, BU significantly protected SK-N-SH cells from 1-methyl-4-phenylpyridinium (MPP⁺) insult, produced striking inhibitory actions on dopamine/norepinephrine uptake and WIN35,428 binding in synaptosomes on in vivo administration, and significantly preventing poor performance on rotarod and dopaminergic loss in substantia nigra in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) mice. BU acts by protecting dopaminergic neurons from MPP⁺ injury and preventing against MPTP-induced behavioral and histological lesions in the Parkinson’s disease (PD) model, possibly by inhibiting monoamine transporters. These findings suggest that BU could be meaningful in PD treatment. Received 14 January 2009; received after revision 22 February 2009; accepted 10 March 2009     

In vitro inactivation of the neurotoxic action of β-bungarotoxin by the marine natural product,manoalide

Summary The irreversible neurotoxic action of -bungarotoxin (-BuTx) can be prevented by preincubation of the toxin with manoalide, a non-steroidal anti-inflammatory agent. Manoalide was also found to inactivate purified phospholipase A₂ and thus prevent hydrolysis of phosphatidylcholine. PLA₂ is a component found in several neurotoxic venoms and is also a rate limiting enzyme important in phospholipid metabolism and prostaglandin synthesis in man.This work is a result of research sponsored in part by NOAA-Department of Commerce under Sea Grant No. NA80AA-D-00120 and the California State Resources Agency R/MP-21. The US Government is authorized to produce and distribute reprints for governmental purposes. A preliminary report of aspects of this work appeared in Fedn Proc.42 (1983) 374. We also acknowledge the technical assistance of Dan Rohrer. Dr George Taborski's advice and assistance during the course of this work is gratefully acknowledged.J. C. de Freitas is a post-doctoral fellow supported by Fundacao de Amparo à Pesquisa do Estado de São Paulo (81/0263-9) and Conselho Nacional de Desenvolvimento Cientifico e Tecnológico (201.171/82), Brazil.     

Enterohepatic cycling of O-(β-hydroxyethyl) rutosides and their biliary metabolites in the rat

Summary O-(-Hydroxyethyl)rutosides are shown to undergo reabsorption from the intestine following their secretion in bile.Acknowledgment. The authors wish to thank Mr P. B. Wood and Mr S. D. Godfrey for skilled technical assistance and Zyma, S. A., Nyon, Switzerland, for financial support.     

An immunohistochemical and ultrastructural comparison of the effects of 2-bromo-α-ergocryptine on intrasellar and transplanted rat pituitaries

Summary Following 2 weeks of administration of 2-bromo--ergocryptine, a marked decrease was observed in prolactin immunoreactivity of the grafted pituitaries, whereas no reduction was noted in the intrasellar pituitaries. No evidence of crinophagy was revealed by electron microscopy in prolactin cells of 2-bromo--ergocryptine-treated rats.Acknowledgments. This work was supported in part by the Medical Research Council of Canada (grant MA-6349). The excellent technical assistance of Mrs Cynthia Edwards and secretarial help of Mrs Wanda Wlodarski are gratefully acknowledged.     

Cytogenetic effects of delta-9-tetrahydrocannabinol (Δ 9-THC) on hamster bone marrow

Summary Single s.c. injections of 10 or 1000 mg/kg of ⁹-THC did not induce discernable chromosomal damage but caused significant mitotic inhibition in the bone marrow of Syrian hamsters.Acknowledgments. The authors which to thank Mr R.H. Graham, Department of National Health and Welfare, Health Protection Branch, for the generous supply of ⁹-THC. This research was supported by a grant to Dr M.G. Joneja from the Department of National Health and Welfare.     

Antiproliferative effects of 4′, 5′-unsaturated adenine nucleosides on leukemia L 1210 cells in vitro

Summary Several 4, 5-unsaturated adenine nucleosides were shown to have antiproliferative activity against L 1210 leukemia cells in vitro. The active nucleosides were cytotoxic to the L 1210 cells as demonstrated by Trypan Blue uptake. The cytotoxicity was not induced by alterations in the ribonucleoside and deoxyribonucleoside triphosphate levels of the L 1210 cells.     

Effect of Fe(Ⅲ) impurity on the electrochemical performance of LiFePO_4 prepared by hydrothermal process

Lithium iron phosphate(LiFePO4)was synthesized from LiOH,FeSO4 and H3PO4 by a hydrothermal process at 180℃.The samples were characterized by X-ray diffraction,scanning electron microscopy and chemical analysis.Electrochemical performance of the samples was tested in terms of charge-discharge capacity and cycling behavior.The results indicated that Fe(Ⅲ) impurity had obviously effect on the electrochemical properties of LiFePO4,and the formation of Fe 3+ was caused by the oxidation of Fe 2+ in the dissolving...     

Antagonism by haloperidol of the suppression of exploratory locomotor activity induced by the local application of(−)3-(3-hydroxyphenyl)-N-n-propylpiperidine into the nucleus accumbens of the rat

Summary The injection of (–)3-PPP into the nucleus accumbens, 10 g/side, produced a suppression of exploratory locomotor activity without affecting treadmill locomotion. Furthermore, the suppression of exploratory locomotor activity produced by (–)3-PPP was antagonized by the administration of haloperidol, 25–50 g/kg i.p.Acknowledgments. The figures were prepared by M. Kröning at the Department of Psychology, University of Göteborg. This work was supported by Torsten and Ragnar Söderberg's Foundation, Magn. Bergvall Foundation and Åke Wiberg Foundation.     

Sertoli cells of adult rats in vitro. II. Effect of different steroid precursors on estradiol 17β-synthesis

Summary The estradiol 17-synthesis by ⁴ pathway has been studied in homogenous cultures of Sertoli cells isolated from adult rat testes. The data reported clearly demonstrate that progesterone, androstenedione, testosterone and estrone induce an increase of the estradiol 17-production.This work was partially supported by grants No. 77.01322.04 and No. 77.01958.04 from the Consiglio Nazionale delle Ricerche.The excellent technical assistance of Antonio Muller and Massimo Rosati is deeply appreciated.     

Effect of paraoxon (diethyl 4-nitrophenyl phosphate) on axone reflex sweating produced byα-lobeline

Zusammenfassung Paraoxon beeinflusst die Wirkung von-Lobelin über den Axonreflex, der Schwitzen menschlicher Haut auslöst. Geringe Konzentrationen von-Lobelin werden durch Paraoxon verstärkt, während höhere gehemmt werden. Daraus wird gefolgert, dass endogenes Acetylcholin an der Auslösung des Axonreflexes beteiligt sein kann.     

On the action ofβ-melanocyte stimulating hormone (β-MSH) on spontaneous electric discharge of the transparent knife fish,G. eigenmannia

Résumé L'hormone mélanophorétique-MSH, à des concentrations de 0.1 à 0.2µg/ml dans l'eau de l'aquarium, produit une diminution de la fréquence des modifications spontanées de l'amplitude des décharges électriques du poissonG. eigenmannia. Ces résultats sont en accord avec les observations antérieures montrant divers effets de-MSH sur l'activité électrique du système nerveux central chez les mammifères.     

The effect of cyclic cytidine 3′,5′-monophosphate (cCMP) on the in vitro development,hatching and attachment of the mouse blastocyst

Summary The in vitro development and attachment of hatched mouse blastocysts on the untreated substratum was enhanced by 10 M dibutyryl cCMP (dbcCMP). The result suggests that cCMP has an effect on embryonic development and on the blastocyst attachment process.25 November1986