Non‐target‐site glyphosate resistance in Conyza bonariensis is based on modified subcellular distribution of the herbicide          下载免费PDF全文

Ziv Kleinman  Baruch Rubin 《Pest management science》2017,73(1):246-253

  相似文献   

Pharmacologic enhancement or suppression of phagocytosis by bovine neutrophils   总被引：4，自引：0，他引：4  

M J Paape  R H Miller  G Ziv 《American journal of veterinary research》1991,52(2):363-366

Sixty-three drugs, belonging to 10 chemical classes, were tested in vitro to determine effects on phagocytosis of 32P-labeled Staphylococcus aureus by neutrophils isolated from milk. Within each class, the number of antibiotics tested were: nonsteroidal anti-inflammatory drugs (NSAID; 8), peptolids (2), aminoglycosides (8), tetracyclines and fusidic acid (4), beta-lactam antibiotics (25), secretolytic agents (2), macrolides (5), polypeptides (2), and antibacterial quinolones (8). Percentage of phagocytosis was determined after incubating (2 hours at 37 C) 12.5 x 10(6) viable neutrophils, 200 x 10(6) 32P-labeled S aureus with antibiotics and 5% skimmed milk. Concentrations of antibiotics tested were 1,000, 500, and 10 micrograms/ml of incubation media. When compared with nonantibiotic controls at the highest drug concentration, the NSAID acetylsalicylic acid and centrophenoxine increased phagocytosis 23.2 and 8.8%, respectively, and benzydamine, indomethacin, phenylbutazone, ibuprofen, and acetominophen decreased phagocytosis 22.8, 14.2, 9.8, 27.0, and 18.2%, respectively. The peptolids novobiocin and pristinamycin decreased phagocytosis 24.5 and 22.0%, respectively. The aminoglycosides tobramycin, amikacin, and gentamicin decreased phagocytosis 21.1, 15.4, and 19.2%, respectively. For the tetracyclines and fusidic acid, minocycline and doxycycline decreased phagocytosis 39.8 and 54.2%, respectively. The beta-lactam antibiotics carfecillin, cephapirin sodium, and cephacetrile sodium decreased phagocytosis 11.2, 12.8, and 23.8%, respectively. The secretolytic agent, bromhexin, increased phagocytosis 10.8%. These data indicate that the potential for enhanced phagocytosis exists through use of some NSAID, and for depressed phagocytosis through use of aminoglycosides, peptolids, tetracyclines, and beta-lactams, as well as certain other NSAID.  相似文献   

Pharmacokinetics and bioavailability of ceftriaxone administered intravenously and intramuscularly to calves   总被引：1，自引：0，他引：1  

S Soback  G Ziv 《American journal of veterinary research》1988,49(4):535-538

Ceftriaxone was administered to Israeli-Friesian male calves by IV and IM routes. The antibiotic was administered IV (10 mg/kg) to 10 calves and IM to 23 calves; 8 were given the antibiotic at the rate of 10 mg/kg of body weight, 5 were given 20 mg/kg, and 10 were given 10 mg/kg, together with probenecid at 40 mg/kg. Serum concentration vs time profiles measured after IV and IM administration were analyzed by use of statistical moment theory. The following mean values +/- SD were found: elimination half-life (t1/2) was 83.8 +/- 8.6 minutes after IV administration and significantly longer 116.8 +/- 20.5 minutes (P less than 0.001) after IM administration at 10 mg/kg. The t1/2 was increased to 141.3 +/- 24.4 minutes by the coadministration of probenecid and to 145.0 +/- 48.2 minutes by doubling the IM dosage to 20 mg/kg. The total body clearance was 3.39 +/- 0.42 ml/min/kg and the renal clearance 2.37 +/- 0.74 ml/min/kg. The specific volume of distribution was 0.2990 +/- 0.0510 L/kg. The average mean residence time (MRT) was 94.0 +/- 12.3 minutes after IV administration and 137.6 +/- 19.9 minutes after IM administration of ceftriaxone at 10 mg/kg. The MRT was increased to 198 +/- 48.8 minutes by the coadministration of probenecid and to 191.0 +/- 59.4 minutes by doubling the IM dose. The former value was significantly different from the MRT after IM administration of the antibiotic at 10 mg/kg. Bioavailability of ceftriaxone after IM administration at 10 mg/kg and at 20 mg/kg was 78% and 83%, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)  相似文献   

Effects of probenecid on blood levels and tissue distribution of ampicillin in fowls and turkeys     

G Ziv  J Neumann  J Fridman  E Ziv  N Singer  A Meshorer 《Avian diseases》1979,23(4):927-939

The effect of probenecid (a benzoic acid derivative which competitively inhibits active secretion of weak organic acids by the renal tubules) on serum ampicillin concentrations and the distribution of ampicillin in body organs was examined in fowls and turkeys. An aqueous solution of probenecid coadministered intramuscularly, at 200 mg/kg, with sodium ampicillin solution, at 25 mg/kg, resulted in peak serum antibiotic concentration of 16.5 microgram/ml. A similar dose of ampicillin administered alone produced a peak level of 4.6 microgram/ml. Subcutaneous injections of sodium ampicillin at 25 mg/kg with aqueous probenecid at 200 mg/kg resulted in a peak serum ampicillin concentration (12.8 microgram/ml) three times as high as the peak produced by the subcutaneous injection of ampicillin alone at 50 mg/kg (4.2 microgram/ml). The elimination half-life (t 1/2) of the drug (30 min) was increased to 1.5 hr by coadministration of probenecid parenterally, and serum antibiotic levels greater than or equal to 5.0 microgram/ml were maintained during 3 hours. Ampicillin seemed to be poorly absorbed from the gastrointestinal tract of fowls. A single oral bolus administration of ampicillin trihydrate aqueous suspension produced a peak of 0.6 microgram/ml, and coadministrations of aqueous probenecid suspension at 20, 50, and 100 mg/kg respectively produced peaks of 0.9, 1.25, and 1.5 microgram/ml. During 4 and 5 days, when ampicillin was added to the drinking water at rates of 200 and 50 mg/liter, serum ampicillin levels were rather low (peaks of 0.20 and 0.12 microgram/ml, respectively), and although these levels were increased by 50% with the coadministration of probenecid they were considered to be of limited clinical value for treating systemic bacterial infections. Probenecid did not change the distribution of ampicillin in the organs.  相似文献   

Vegetative propagation of Alstroemeria in vitro     

Meira Ziv  Rony Kanterovitz  A.H. Halevy 《Scientia Horticulturae》1973,1(3):271-277

Young actively growing tissue explants from Alstroemeria inflorescence stem taken at a distance of 1–2 mm below the apex are capable of regenerating buds and roots from which small plantlets can be established. Root and bud regeneration was directly from the stem tissue and not from the callus. White's medium supported growth and regeneration as well as Murashige & Skoog's medium. A higher ratio of auxin to cytokinin resulted in root regeneration, while the reversed ratio promoted bud differentiation. Plantlets were obtained upon bud subculture on a low sucrose medium supplemented with indoleacetic acid but without kinetin.  相似文献   

Serum and milk concentrations of apramycin in lactating cows, ewes and goats   总被引：2，自引：1，他引：1  

G. Ziv  B. KURTZ  R. RISENBERG  A. GLICKMAN 《Journal of veterinary pharmacology and therapeutics》1995,18(5):346-351

A 20% solution of apramycin was administered intravenously (j.v.) and intramuscularly (i.m.) to lactating cows with clinically normal and acutely inflamed udders, to lactating ewes with normal or subclinically infected, inflamed udders and i.v. to lactating goats with normal udders. The i.v. disposition kinetics of apramycin was very similar in cows, ewes and goats. The elimination half-life was approximately 2 h and the steady-state volume of distribution was 1.26–1.45 L/kg. The absorption rate of the drug from the i.m. injection site was rapid, the i.m. bioavailability was 60–70% and the mean elimination half-life was 265 min in cows and 145.5 min in ewes. The binding percentage of apramycin to serum protein was low (< 22.5%). Concentrations of apramycin in milk produced by clinically normal mammary glands of cows, ewes and goats were consistently lower than in serum; the kinetic value AUC _milk/ AUC _serum was < 0.32. Drug penetration into the milk from the acutely inflamed quarters of cows was extensive; mastitis milk C _max values were more than tenfold greater than the C _max in normal milk. On the other hand, the drug had limited access to the milk produced by subclinically infected inflamed half-udders of ewes.  相似文献   

Abstracts Of Papers Presented at A joint UK — Hebrew University Of Jerusalem (HUJ) Seminar On     

J. Katan  D. C. Harris  A. Sztejnberg  O. Yarden  Adi Beth Din  Vered Ziv  Einat Yatzkan  Rena Gorovits  J. P. Blakeman  G. W. Cussans  B. Rubin  A. J. M. Baker  Hedva Schickler  Hadar Caspi  G. M. Gadd  M. M. Gharieb  Jacqueline A. Sayer  Amanda R. Whatley  C. White 《Phytoparasitica》1998,26(4):331-360

  相似文献   

Preliminary clinical pharmacological investigations of tylosin and tiamulin in chickens     

Ziv G 《The Veterinary quarterly》1980,2(4):206-210

Summary The minimal inhibitory concentrations (M1C) of tiamulin and tylosin for mycoplasma. Gram-positive, and Gram-negative micro-organisms isolated from chickens were determinated by the agar dilution method. Median M1C values for tiamulin against Mycoplasma gallisepticum (0.05 μg/ml) and Mycoplasma synoviae (0.10 μg/ml) were 2 to 4 times lower than the corresponding values for tylosin. Tiamulin was also slightly more effective in vitro in inhibiting Escherichia coli, Pasteurella multocida, and beta-haemolytic streptococci than was tylosin. Groups of chicken were offered tiamulin medicated drinking water at rates of 125 and 250 mg/litre for 48 hours. Average serum tiamulin concentrations were 0.38 and 0.78 μg/ml, respectively. When tylosin tartrate was added to the drinking water at 500 and 700 mg/litre, average serum drug levels were 0.12 and 0.17 μg/ml, respectively. Tiamulin was 45% bound in chicken serum, as against 30% serum protein binding or tylosin. Correlations were made between free (non protein bound) serum drug levels and the MIC values of the two drugs. Such comparisons suggest that when tiamulin is given in the drinking water at rates of 125 to 250 mg/litre, better antimycoplasmal activity is to be expected in vivo than by giving tylosin tartrate in the drinking water at 500 to 700 mg/litre. Based on these data, no clinical efficacy of these dose rates can be expected in flocks infected by gram-negative microorganisms such as E. coli or P. multocida. The tylosin tartrate rate of 500 to 700 mg/litre, may be clinical ineffective the treatment of Staphylococcus aureus infections.  相似文献   

Pharmacological aspects of chloramphenicol administration by the intramammary route to lactating dairy cows     

Nouws JF  Ziv G 《The Veterinary quarterly》1982,4(1):23-31

Concentrations of chloramphenicol (C M) were determined, by microbiological assay, in the milk and blood serum of 17 culled dairy cows after intramammary infusion of an approved parenteral CM product (Gloveticol) and in the milk of 16 lactating cows after treatment with two approved CM products for intramammary infusion, at dosages ranging from 1 to 30 g/cow. C M was quickly absorbed from the udder into the blood circulation; the doses of 12.5 and 25 g/cow were almost completely absorbed within 20 hours. Absorption half-life (t1/2ab) from fully functioning quarters was 57+/-18 minutes, and the t1/2ab from partially functioning quarters was 125+/-37 minutes. Mean peak serum C M concentrations were 6.1, 16.2, and 37.4 microg/ml after the cows had been infused with 5, 12.5, and 25 g, respectively. These values were considerably higher than the corresponding peak serum C M concentrations reported following intramuscular injection of equivalent doses of the drug. C M residues were not detectible microbiologically in milk from treated quarters 20 hours after treatment with 5 g or 6.25 g, and 36 hours after treatment with 15 g. Drug concentrations in the milk from the non-treated quarters were approximately 70 per cent of the corresponding serum drug levels. Serum CM concentrations of potential therapeutic value in the treatment of gram-negative bacterial infections, i.e. > 5 microg/ml, were maintained for 8 hours after cows had been infused with 12.5 g, and for 12 hours after infusion with 25 g. The implications of the improved systemic availability of C M infused by the intramammary route over the intramuscular route are discussed in terms of potential therapeutic efficacy, local irritation, and duration of drug residues.  相似文献   

The influence of connectivity on richness and temporal variation of reef fishes     

Jonathan Belmaker  Yaron Ziv  Nadav Shashar 《Landscape Ecology》2011,26(4):587-597

To test the effects of connectivity on fish diversity in isolated reef patches we deployed pairs of artificial reefs (AR) at constant distances (12 and 25 m) from a large continuous reef and added series of small ARs to half of them. These small reefs served as stepping-stones to increase fish movement between the large ARs and the continuous reef. Species gain and loss curves were compared to obtain deeper understanding of the underlying mechanisms in relation to the theory of island biogeography. We found that AR without stepping-stones maintained up to 57-fold more individuals than ARs with stepping-stones during mass recruitment events that were dominated by the family Apogonidae. However, in-between these mass recruitment events the overall impact of the stepping-stones on richness and abundance was small. By contrast, increasing distance from the continuous reef from 12 to 25 m increased fish richness, although this was confounded with time since AR deployment. Increase in richness with distance was predominantly caused by elevated species gain. Our results suggest that fish assemblages respond in distinct ways to two types of isolation: (1) Increased richness with distance from a continuous reef, and (2) increased fluctuation in abundance with decreased connectivity. The latter may be the outcome of accumulation and then abrupt emigrations of fishes from isolated reefs. This study confirms that the spatial setting of reef patches in relation to larger or continuous reefs alters fish assemblages, which may be important for planning AR deployments that maximizes diversity.  相似文献