Microwave treatment of intracerebral l1210 leukemia: Schedule-dependent partial reversal of the effects of methotrexate

One-GHz microwave (MW) irradiation at a power density of 5 mW/cm² was combined with methotrexate (MTX) in an attempt to treat more effectively central nervous system (CNS) L1210 leukemia in DBA/2J mice. When mice with CNS leukemia were treated with the combination of MW and MTX, there was no improvement in survival compared with a group of animals treated with MTX alone; however, the group that received MTX before the MW exposure had a significantly reduced survival time compared with the group treated with MTX alone or with the group to which MTX was administered after MW.     

Prostacyclin analogues inhibit canine parietal cell activity and cyclic AMP formation

To assess further the mechanism by which prostacyclin inhibits acid secretion, the actions of two stable prostacyclin analogues on parietal cell function and cyclic AMP formation were tested using enzymatically dispersed cells from canine fundic mucosa. Accumulation of ¹⁴C-aminopyrine (AP) was used as an index of parietal cell response to stimulation. The 16-phenoxy derivative of PGI₂ inhibited accumulation of AP stimulated by histamine (10 μM), with 50% inhibition (ID₅₀) at 10 nM. 6_β-PGI₁ also inhibited the action of histamine (ID₅₀ 0.5μM) but failed to block stimulation by carbachol or the dibutyryl derivative of cyclic AMP (dbcAMP). In similiar concentrations to those producing inhibition of histamine-stimulated AP accumulation, the 16-phenoxy analogue and 6_β-PGI₁ inhibited histamine-stimulated cyclic AMP generation by parietal cells. At 100 fold higher concentrations, 6_β-PGI₁ stimulated cyclic AMP formation, presumably in non-parietal cells. Even in high concentrations the 16-phenoxy analogue failed to increase cyclic AMP formation by mucosal cells. These data indicate that the stable prostacyclin analogues are potent, direct inhibitors of histamine-stimulated parietal cell function and that it is the inhibition, rather than the stimulation, of cyclic AMP formation that is linked to the antisecretory actions of these prostanoid compounds.     

Behavioural ecology of the Sloth bear (Melursus ursinus)

The Sloth bear ( Melursus ursinus ), which is endemic to the Indian subcontinent and Sri Lanka, has declined in numbers in many areas in recent years probably as the result of over-killing and habitat alteration. In the 544 km² Royal Chitawan National Park in the Nepal terai, we estimated there were a minimum of 55 bears or a crude density of 0˙1/km². During peak concentrations in the lowlying riverine forest/tall grass habitat in March, the ecological density was 0˙5/km².
Cubs still with their mothers comprised 24 % of the 161 bears classified between December 1972 and November 1975. Females comprised 48% of the adults classified. Average size of 24 litters was 1˙6 (1–2). Seventy-two per cent of the observations were of lone individuals. Three (an adult female with two cubs), was the largest group of bears seen. The only extended social group observed was the female-young unit although newly independent siblings may remain together for a short time. Maternal relations, adult interactions, tree marking, ranging, feeding and anti-predatory behaviour are described.
Examination of 139 droppings showed that these bears fed on at least 17 different fruits (47% occurrence), flowers, grass, honey, and six different insects (52% occurrence). Fruits were an important food from March to June with individual species predominating throughout their fruiting season. Termites, including Odontotermes obesus , were in the diet for most of the year. The Sloth bear was not observed preying on mammals and according to other observers, only rarely feeds on carrion. The ecological basis for selected aspects of Sloth bear biology and behaviour is discussed.     

Tomato alcohol dehydrogenase: Purification and substrate specificity

Alcohol dehydrogenase of tomato (Lycopersicon esculentum) has been purified to homogeneity, using affinity chromatography on Cibacron F3GA-agarose. The enzyme is a dimer, M_r 90,000–100,000. The coenzyme is NAD⁺; no NADP⁺-dependent activity was detected even in crude extracts. Among saturated substrates, ethanol and acetaldehyde show the lowest apparent K_m values (2.67 and 0.174 mm, respectively) and highest V values, supporting a primary role in acetaldehyde metabolism, with action also on “flavor aldehydes”; 2-unsaturated alcohols show still lower K_m values, probably due to a more favorable K_eq. This enzyme and other plant alcohol dehydrogenases form a definite class, intermediate in specificity between liver and yeast alcohol dehydrogenases: they differ from the former in being essentially inactive on secondary and aromatic substrates, from the latter in showing only a mild decrease in V with increasing chain length of alkyl substrates, and from both in showing the lowest K_m as well as highest V on ethanol and acetaldehyde. The tomato enzyme differs from other reported plant enzymes in showing substantial activity on geraniol. Kinetic studies are in agreement with an ordered sequential mechanism. The enzyme is inhibited slowly by iodoacetamide, and reversibly by acetamide and zinc-chelating compounds.