Synthesis and biological activity of furanyl anti-juvenile hormonal compounds     

William S. Bowers  Gopalan C. Unnithan  Jun-Ichi Fukushima  Jun Toda  Takeyoshi Sugiyama 《Pest management science》1995,43(1):1-11

Twenty-one synthetic compounds, containing one or more furan rings, were demonstrated to possess anti-juvenile hormone (AJH) activity as evidenced by their induction of premature metamorphosis in the milkweed bug, Oncopeltus fasciatus (Dallas) by contact, topical application or fumigation. The ED₅₀ of the four most active analogs required to induce precocious metamorphosis from 3rd-instar nymphs by residue contact in a Petri dish compared favorably with that of precocene II (6,7-dimethoxy-2,2-dimethyl 2H-chromene) a naturally occurring phytochemical AJH. Precocious metamorphosis was fully reversible by co-treatment with juvenile hormone (JH III) or JH analogs, demonstrating that the observed AJH activity resulted from an induced deficiency of juvenile hormone.  相似文献   

Nonendoscopic Antegrade Percutaneous Gastrostomy: The Effect of Preplacement Gastric Insufflation on Tube Position and Intra-Abdominal Anatomy   总被引：1，自引：0，他引：1  

Erik M. Clary  Elizabeth M. Hardie  William D. Fischer  rew E. Kyles 《Journal of veterinary internal medicine / American College of Veterinary Internal Medicine》1996,10(1):15-20

Nonendoscopic tube gastrostomy was performed on 41 anesthetized dogs using the technique of Fulton and Dennis with or without gastric insufflation prior to tube placement. Immediately after tube placement, dogs were euthanized and postmortem examinations performed. When gastric insufflation was not performed (group I), gastrostomy tubes penetrated the visceral surface of the stomach in 25% of dogs. The deep leaf of the omentum was interposed between stomach and body wall in the majority of these dogs, exposing other intra-abdominal organs to potential injury. Additionally, displacement and tethering of the spleen cranial to the gastrostomy site were observed in 33% of dogs in group I. Similar results were obtained when preplacement gastric insufflation was performed after the orogastric tube was inserted sufficiently far to displace the stomach laterally against the body wall (group II). In contrast, consistent positioning of gastrostomy tubes through the parietal surface of the stomach was achieved when the stomach was insufflated prior to lateralizing the left abdominal wall with the gastric end of the orogastric tube (group III). It was concluded that the blind percutaneous gastrostomy technique is made safer by insufflating the stomach immediately prior to pushing the gastric wall laterally into contact with the parietal peritoneum. J Vet Intern Med 1996;10:15–20. Copyright © 1996 by the American College of Veterinary Internal Medicine .  相似文献   

Lung Lobe Torsion in the Cat     

Nancy O.  Brown William J.  Zontine 《Veterinary radiology & ultrasound》1976,17(6):219-223

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ANESTHESIA FOR THE TRAUMATIZED PATIENT     

William V. Lumb D.V.M.  M.S.  Ph.D.  † 《Veterinary surgery : VS》1974,3(3):49-50

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Biphenyl hydroxylation and its induction differ between montane voles and Swiss Webster mice     

Moheb H. Makary  William A. Brindley 《Pesticide biochemistry and physiology》1983,19(1):23-30

Hepatic microsomes from female montane voles, Microtus montanus, metabolized biphenyl to 4-hydroxybiphenyl (359 ng/mg microsomal protein/min), 3-hydroxybiphenyl (49 ng/mg/min), and 2-hydroxybiphenyl (29 ng/mg/min). Phenobarbital treatment of the voles (ip) induced in vitro biphenyl hydroxylations by about 324, 865, and 445% for 4-, 3- and 2-hydroxylation, respectively. Comparable studies were made of female, white Swiss Webster mice. The major microsomal metabolite was 4-hydroxybiphenyl (1010 ng/mg/min) but more 2-hydroxybiphenyl (118 ng/mg/min) was formed than 3-hydroxybiphenyl (92 ng/mg/min). Phenobarbital treatment of the mice barely changed biphenyl 2-hydroxylation (?1.3%) but did raise 3- and 4-hydroxylation (55 and 211%, respectively). Treatment of voles with 3-methylcholanthrene raised biphenyl 2-, 3-, and 4-hydroxylation by about 81, 50, and 47%, respectively, whereas in mice the increases were 176, 41, and 31%, respectively. β-Naphthoflavone treatment had similar effects. The vole liver microsomes were dependent upon NADPH for biphenyl hydroxylation. The carbon monoxide difference spectra of reduced cytochrome in the microsomes show a peak at 450.4 nm. This was unchanged by phenobarbital and only slightly shifted (?0.8 nm) by 3-methylcholanthrene or β-naphthoflavone treatment. Voles and mice represent different families of the order Rodentia. The results obtained with voles more closely resemble those reported for hamsters which are in the same family but a different subfamily than voles. Comparative consideration of the taxonomic relations of the rodents, therefore, may be useful in interpreting their comparative toxicology.  相似文献   

Effects of growth factors (EGF,PDGF-BB and TGF-beta 1) on cultured equine epithelial cells and keratocytes: implications for wound healing     

Haber M  Cao Z  Panjwani N  Bedenice D  Li WW  Provost PJ 《Veterinary ophthalmology》2003,6(3):211-217

Objective The physiologic mechanisms involving growth factors, including PDGF‐BB, EGF, and TGF‐β1, as potent mediators of fibroblasts and epithelial cells in corneal wound healing remain unknown. The goal of this study was to determine culture methods for equine epithelial cells and keratocytes and to investigate how exogenous growth factors influence proliferation of both cell types. Procedures Cell cultures were established from healthy corneas harvested from horses immediately following euthanasia and maintained using standard tissue culture protocols. To determine the effects of PDGF‐BB, EGF, TGF‐β1, keratocytes (1 × 10⁵/well) and epithelial cells (2 × 10⁵/well) were each cultured in 12 well plates and exposed separately to the growth factors. The cells were exposed to concentrations of EGF between 0 and 50 ng/mL; PDGF‐BB between 0 and 75 ng/mL; and TGF‐β1 between 0 and 10 ng/mL. Cell proliferation was measured using ³H‐thymidine assay and differences in growth determined using anova and Tukey's HSD test (P < 0.05). Results Epithelial cell and keratocyte cultures were successfully established. EGF maximally stimulated keratocyte and epithelial cells at 25 ng/mL and 5 ng/mL, respectively. PDGF‐BB maximally stimulated keratocytes and epithelial cells at 50 ng/mL and 5 ng/mL, respectively. TGF‐β1 inhibited keratocytes at 5 ng/mL and 10 ng/mL, and epithelial cells at 1 ng/mL and 2 ng/mL. Conclusions Methods were established to maintain epithelial cells and keratocytes in vitro. PDGF‐BB and EGF stimulate, while TGF‐β1 inhibits the proliferation of epithelial cells and keratocytes. These growth factors may play a role in maintenance and repair of the equine cornea.  相似文献   

Flash electroretinography in standing horses using the DTL microfiber electrode     

Komáromy AM  Andrew SE  Sapp HL  Brooks DE  Dawson WW 《Veterinary ophthalmology》2003,6(1):27-33

Purpose The goal of our study was the evaluation of a practical method for the recording of flash electroretinograms (ERGs) in sedated, standing horses with the DTL? microfiber electrode. Methods The horses were sedated intravenously with detomidine hydrochloride (0.015 mg/kg). The pupil was dilated and the auriculopalpebral nerve was blocked. The ERGs were recorded with the active electrode on the cornea (DTL?), the reference electrode near the lateral canthus, and the ground electrode over the occipital bone. The light intensities of the white strobe light were 0.03 cd·s/m² (scotopic) and 3 cd·s/m² (scotopic and photopic). Photopic and scotopic single flash and flicker responses to Ganzfeld stimulation were recorded. During the 20‐min dark adaptation period the retina was stimulated every 5 min with the 0.03 cd·s/m² single flash. Results The median b‐wave amplitudes and implicit times were 38 µV and 33 ms (photopic cone‐dominated response), 43 µV and 63 ms (5‐min dark adaptation), 72 µV and 89 ms (10 min), 147 µV and 103 ms (15 min), 188 µV and 109 ms (20 min, 0.03 cd·s/m², rod response), and 186 µV and 77 ms (20 min, 3 cd·s/m², maximal combined rod‐cone response). A steady increase in amplitude and implicit time was noted during dark adaptation. No oscillatory potentials could be isolated. Conclusions The use of detomidine hydrochloride sedation and the DTL? microfiber electrode allowed the recording of good quality ERGs. This protocol should permit the detection of functional problems in the retina without the risk involved with general anesthesia.  相似文献   

Detection, quantification, and pharmacokinetics of furosemide and its effects on urinary specific gravity following IV administration to horses     

Dirikolu L  Lehner AF  Hughes C  Karpiesiuk W  Camargo FC  Harkins JD  Woods WE  Bosken JM  Boyles J  Troppmann A  Fisher M  Tobin T 《Veterinary therapeutics : research in applied veterinary medicine》2003,4(4):350-363

Furosemide is a potent loop diuretic used for the prevention of exercise-induced pulmonary hemorrhage in horses. This drug may interfere with the detection of other substances by reducing urinary concentrations, so its use is strictly regulated. The regulation of furosemide in many racing jurisdictions is based on paired limits of urinary SG (<1.010) and serum furosemide concentrations (>100 ng/ml). To validate this regulatory mechanism, a liquid chromatography/mass spectrometry/mass spectrometry method employing a solid-phase extraction procedure and furosemide-d5 as an internal standard was developed. The method was used to determine the pharmacokinetic parameters of furosemide in equine serum samples and its effects on urinary SG after IV administration (250 mg) to 10 horses. Pharmacokinetic analysis showed that serum concentrations of furosemide were well described by a two-compartmental open model. Based on results in this study, it is very unlikely for horses to have serum furosemide concentrations greater than 100 ng/ml or urine SG less than 1.010 at 4 hours after administration (250 mg IV). However, it should be remembered that urine SG is a highly variable measurement in horses, and even without furosemide administration, some horses might naturally have urine SG values less than 1.010.  相似文献   

Analysis of genotypic diversity data for populations of microorganisms     

Grünwald NJ  Goodwin SB  Milgroom MG  Fry WE 《Phytopathology》2003,93(6):738-746

ABSTRACT Estimation of genotypic diversity is an important component of the analysis of the genetic structure of plant pathogen and microbial populations. Estimates of genotypic diversity are a function of both the number of genotypes observed in a sample (genotype richness) and the evenness of distribution of genotypes within the sample. Currently used measures of genotypic diversity have inherent problems that could lead to incorrect conclusions, particularly when diversity is low or sample sizes differ. The number of genotypes observed in a sample depends on the technique used to assay for genetic variation; each technique will affect the maximum number of genotypes that can be detected. We developed an approach to analysis of genotypic diversity in plant pathology that makes specific reference to the techniques used for identifying genotypes. Preferably, populations that are being compared should be very similar in sample size. In this case, the number of genotypes observed can be used directly for comparing richness. In most cases, sample sizes differ and use of the rarefaction method to calculate richness is more appropriate. In all cases, scaling either Stoddart and Taylor's G or Shannon and Wiener's H' by sample size should be avoided. Under those circumstances where it might be important to distinguish whether richness or evenness contribute more to diversity, a bootstrapping approach, where confidence intervals are calculated for indices of diversity and evenness, is recommended.  相似文献   

Effect of Variable Temperature on Infection Severity of Podosphaera macularis on Hops     

Mahaffee WF  Turechek WW  Ocamb CM 《Phytopathology》2003,93(12):1587-1592

ABSTRACT The effect of variable temperature on the infection severity of Podosphaera macularis was investigated. Potted 'Symphony' hop plants were inoculated and exposed to different temperature regimes that included supraconducive temperatures (30 to 42 degrees C) for varying periods of time (2 to 9 h). Infection severity (lesions per cm(2) of leaf area) was calculated 7 to 10 days after inoculation. Immediately exposing inoculated plants to 30 degrees C for as little as 2 h significantly (P 相似文献