Changes in fetal mannose and other carbohydrates induced by a maternal insulin infusion in pregnant sheep

Background: The importance of non-glucose carbohydrates, especially mannose and inositol, for normal development is increasingly recognized. Whether pregnancies complicated by abnormal glucose transfer to the fetus also affect the regulation of non-glucose carbohydrates is unknown. In pregnant sheep, maternal insulin infusions were used to reduce glucose supply to the fetus for both short(2-wk) and long(8-wk) durations to test the hypothesis that a maternal insulin infusion would suppress fetal mannose and inositol concentrations. We also used direct fetal insulin infusions(1-wk hyperinsulinemic-isoglycemic clamp) to determine the relative importance of fetal glucose and insulin for regulating non-glucose carbohydrates.Results: A maternal insulin infusion resulted in lower maternal(50%, P < 0.01) and fetal(35-45%, P < 0.01) mannose concentrations, which were highly correlated(r2= 0.69, P < 0.01). A fetal insulin infusion resulted in a 50% reduction of fetal mannose(P < 0.05). Neither maternal nor fetal plasma inositol changed with exogenous insulin infusions.Additionally, maternal insulin infusion resulted in lower fetal sorbitol and fructose(P < 0.01).Conclusions: Chronically decreased glucose supply to the fetus as well as fetal hyperinsulinemia both reduce fetal non-glucose carbohydrates. Given the role of these carbohydrates in protein glycosylation and lipid production, more research on their metabolism in pregnancies complicated by abnormal glucose metabolism is clearly warranted.     

The use of a medetomidine,butorphanol and atropine combination to enable blood sampling in young pigs

AIM: To determine the suitability of a reversible, injectable anaesthetic combination including medetomidine, butorphanol and atropine to produce the degree of immobilisation required to allow blood sampling in young pigs.

METHODS: Twenty 6-week-old crossbred, intact male pigs were sedated with an intramuscular (I/M) injection of 80 µ'g/kg medetomidine, 200 µ'g/kg butorphanol and 25 µ'g/kg atropine. Heart and respiratory rates and rectal temperatures were monitored. Excessive salivation, gagging, laryngeal reflex, presence of pedal reflex and deep and surface analgesia were noted. Time of injection and the time when pigs reached mild and full sedation were also recorded.

RESULTS: Mild sedation was produced in 90% of pigs after 5.6 (SEM 0.96) min (n=18; median 5, range 2–16 min), and full sedation (lateral recumbency and loss of jaw tone) in 60% of pigs after 12.5 (SEM 2.14) min (n=12; median 10, range 5-28 min). The depth and duration of sedation were very variable and most animals were easily aroused. Ninety percent of the animals required the administration of halothane by mask to allow blood sampling, but the amount of halothane required was small. Heart and respiratory rates decreased (p<0.001) but remained within the normal range. Rectal temperature was above normal at the time of sedation and at the time of blood sampling when the ambient temperature was 29° C but not when the ambient temperature was reduced to 25°C.

CONCLUSIONS: The combination of medetomidine, butorphanol and atropine at these doses produced sedation of variable depth and duration that was insufficient on its own to allow blood sampling in the majority of pigs. Hyperthermia can occur in temperature-controlled environments when using medetomidine, butorphanol and atropine in pigs. Reduction of stress and a quieter environment may improve the effects of the anaesthetic combination.     

Carnivorous mushrooms

Ten species of gilled fungi, including the oyster mushroom (Pleurotus ostreatus), have been shown to attack and consume nematodes. It is suggested that these wood-decay fungi utilize the nutrients in their prey to supplement the low levels of nitrogen available in wood. This mode of nutrition is similar in principle to that of carnivorous higher plants.     

A 10-year record of the weathering rates of surficial pebbles in Kärkevagge, Swedish Lapland

Between 1999 and 2004, nylon mesh bags containing  6.2 mm diameter fragments of crushed dolomite or granite were exposed to weathering on the surfaces of birch, Dryas heath, heath, meadow, solifluction meadow, and willow vegetation communities in Kärkevagge, a glaciated trough in Swedish Lapland. The material in the bags had previously been in the same locations from either 1994 or 1995 when it had been placed in the field as freshly crushed pebbles. Results of the mass losses resulting from chemical weathering during the first 4- or 5-year period were reported in Dixon et al. [Dixon, J.C., Thorn, C.E., Darmody, R.G., Schlyter, P. 2001. Weathering rates of fine pebbles at the soil surface in Kärkevagge, Swedish Lapland. Catena 45, 273–286.] in Catena. The spatial results of the second 5-year period confirm those determined during the first period. In general, wetter, more acidic sites promoted greater losses from the dolomite, but the losses from the granite were too small to reveal distinctive spatial patterns. Dolomite consistently weathered faster than granite in at-a-site comparisons with total mass losses between 1999 and 2004 ranging from 1.90% to 9.98% for dolomite and − 0.07% to 4.02% for granite. Spatial distinctions were blurred during the second period due to significant losses of bags at dry sites from atmospheric exposure. However, at-a-site comparisons between the two study periods revealed statistically significantly greater losses during the second period when compared to the first. In the absence of appropriate ground climate data, it is worth noting that air climates were both warmer and wetter during both study periods when compared to the 1961–1990 averages, and the second 5-year study period was also warmer and wetter than the first.     

Conversion of atrial dissociation with lidocaine in a dog

A 3-year-old healthy dog was presented for abdominal surgery following ingestion of razor blades. An electrocardiogram revealed a regular sinus bradycardia with normal P waves at a heart rate of 45 bpm. In addition, low-amplitude positive deflections (p′ waves) were visualized at a regular interval and rapid rate of 250 bpm, dissociated from the normal sinus P waves. A tentative diagnosis of atrial dissociation was proposed. Administration of lidocaine abolished the p′ waves. This case describes atrial dissociation observed following premedication that was successfully terminated using lidocaine in a healthy dog.     

Thiophene carboxamide fungicides: Structure-activity relationships with the succinate dehydrogenase complex from wild-type and carboxin-resistant mutant strains of Ustilago maydis

A variety of thiophene carboxamide compounds have been synthesized and tested on the succinate dehydrogenase complex (SDC) in mitochondria from a wild-type strain and carboxin-resistant strains of Ustilago maydis (corn smut). The site of action of thiophene carboxamides is identical to that of carboxin (5,6-dihydro-2-methyl-1,4-oxathiin-3-carboxanilide) and thenoyltrifluoroacetone, that is, the succinate-ubiquinone reductase (complex II) span in the mitochondrial electron transfer chain. This investigation reveals new molecular structures which are strong inhibitors of wild-type and carboxin-resistant SDCs. The 5-amino analog of the parent anilide, 3-methylthiophene-2-carboxanilide (I), proved to be an especially potent inhibitor of the wild-type SDC (I₅₀, 0.019 μM). Analogs of (I) such as 4′-carboethoxy, 4′-nbutyl, 4′-phenyl, and 4′-benzoyl were negatively correlated in activity to the carboxanilide (I) with respect to resistance level. A number of structures showed considerable selectivity for mutated SDCs from both highly and (particularly) moderately carboxin-resistant SDCs of U. maydis, markedly lowering the resistance level, i.e., the degree of resistance. Thus, in addition to the oxathiins, specific structural groups of thiophene carboxamides can also alleviate or reverse the effect of carboxin-selected mutation with reference to inhibition of the SDC. Of important significance was the finding that molecular selectivity for mutated, carboxin-resistant SDCs can be influenced by replacement of an oxathiin by a thiophene heterocyclic ring as well as by the substitutive group on the amide nitrogen, permitting different categories of mutant types and even mutants within a single category to be distinguished from one another. With all the structural combinations available, it appears quite possible, in terms of inhibition, to overcome any type of mutation in a fungal SDC which arises through selection by carboxin or other carboxamide compounds. A reasonable correlation generally exists between inhibition by thiophene carboxamides of the SDC and sporidial growth of wild-type and carboxin-resistant strains of U. maydis. A permeability barrier to 4′-substituted analogs of (I) was encountered in the wild-type strain but not mutant strains. Excellent protectant activity against bean rust (Uromyces phaseoli) was obtained with the 3′-nhexyl, 3′-nhexyloxy, and 4′-phenoxy analogs of (I).