Changes in steryl lipids of oat root cells as a function of water-deficit stress

Five-day-old seedlings of oat ( Avena saliva L. cv. Seger) were subjected to water-deficit stress for two and four periods, each of 24h duration with interjacent rewatering periods of 24 h. After two and tour stress periods the fresh weight/dry weight ratio of the roots was 73 and 74% of the control value, respectively. Two stress periods did not affect the amount or composition of free, esterified and glycosylated sterols (desmethylsterols) or methylsterols (mono- and dimethylsterols). After four stress periods the amount of tree sterols increased by 25% on a dry-weight basis but that of free methylsterols only slightly. The most significant increase (by over 60%) occurred in esterified sterols and methylsterols. The amount of sterols bound as glycosides and acylaled glycosides decreased slightly (by 10%) after four stress periods. The amount of glycosylated methylsterols was negligible and did not respond to water-deficit stress. Within all component groups the proportions of individual compounds remained unaffected after two and four stress periods. The increase of the sterol levels caused by the stress is discussed in terms of a hormone-induced synthesis leading to a changed sterol/membrane acyl lipid ratio. This has implications for the chemo-physical properties of the root cell membranes.     

Anticonvulsant activity of 2-phthalimidoethanesulphonamides: New derivatives of taurine

A number of 2-phthalimidoethanesulphonamides, new derivatives of the inhibitory neuromodulator taurine, were tested for their anticonvulsant activity in maximal electroshock seizure and pentetrazole seizure threshold tests in mice. Certain lower N-alkylamides showed activity, methylamide, dimethylamide and isopropylamide derivatives and the unsubstituted amide being pharmacologically most promising. Possible interferences with the intracellular uptake, release and membrane binding of taurine and GABA were assessed in an attempt to elucidate their mode of action. Since the uptake and release processes were only minimally affected, but the sodium-independent binding of GABA and/or taurine to synaptic membranes strongly reduced, the compounds studied may preferentially act as taurine or GABA receptor agonists.     

Polyunsaturated hydrocarbons from Polytrichum commune spores

Polytrichum commune Hedw. spores were found to contain the polyunsaturated hydrocarbons normal all-cis-6,9,12,15-heneicosatetrane (20· ± 0·5 μg/100 mg spores) and normal all-cis-3,6,9,12,15-heneicosapentaene (22·5 ± 1·2 μg/100 mg spores), N- alkanes were present only in minor amounts.     

Esterified long-chain hydroxy acids in green and senescent parts of the peat moss Sphagnum fuscum

The bifunctional long-chain acids in extracts and alkaline hydrolysates of extractive-free tissues from the green and senescent parts of Sphagnum fuscum were investigated by GC and GC/MS. A series of C₁₄– C₂₆hydroxy acids was liberated by alkaline hydrolysis of senescent tissue demonstrating the presence of insoluble polymeric lipid esters in the moss. In the corresponding hydrolysates of the topmost green parts of the shoot the amounts of these acids were significantly smaller. It is suggested that the presence of such polymeric esters in S. fuscum contributes to the cell-wall resistance of this peat-forming moss.     

l-Carnitine uptake by mouse brain synaptosomal preparations: Competitive inhibition by GABA

The uptake ofl-carnitine was characterized in mouse brain synaptosomal preparations, with an emphasis on mutual interactions with GABA uptake systems. The uptake consisted of nonsaturable diffusion and one saturable energy- and sodium-dependent component. GABA,l-DABA and nipecotate were strong and hypotaurine and homotaurine moderate inhibitors of the uptake. The inhibition by GABA was shown to be competitive. GABA uptake contained two saturable transport components, high- and low-affinity. It was most strongly inhibited by nipecotate andl-DABA, but also by carnitine and hypotaurine. The high-affinity uptake of GABA was competitively inhibited by carnitine, but the inhibition of the low-affinity uptake of GABA was of the mixed type. The results suggest that GABA and carnitine share the same carrier system at synaptosomal membranes. However, GABA is the preferred substrate and the carnitine concentrations which significantly inhibited GABA uptake exceed the physiological carnitine levels in vivo.