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1.
Plasma membrane 5'-nucleotidase (5'NT) activity was assayed in lymph node lymphocytes from seven normal control dogs and in malignant lymphocytes from 25 dogs with lymphoma. The lymphoid tumors were classified according to the NCI Working Formulation into five histologic subtypes. When compared with normal controls significantly lower 5'NT activities were found in the lymphoblastic, small lymphocytic and diffuse large (noncleaved) subtypes while no significant differences were observed in the immunoblastic or small noncleaved groups. In addition, dogs with hypercalcemia or paraproteinemia had decreased 5'NT levels. However, no significant differences were found between prognostic groups or histologic subtypes of the NCI classification. In conclusion, canine lymphoma subtypes had generally decreased 5'NT activities which appeared to reflect the B or T cell lineage, degree of maturation and enzyme activity of the cell of origin.  相似文献   

2.
The purpose of this study was to determine the applicability of the Accu-Chek Easy (ACE) human self-monitoring system for monitoring glycemic status in cattle. The ACE method was compared with the Yellow Springs Instrument (YSI) analytical laboratory method in two studies. A preliminary study (62 samples) and a primary study (434 samples) involved a nine-fold range and a 10-fold range, respectively, of glucose concentrations obtained during the acute phase response of growing beef cattle to injections of varying dosages of endotoxin. The ACE monitoring method compared with the YSI analytical method resulted in similar patterns of glucose concentration change, similar ranking of glucose means across endotoxin dosages during hyper-and hypoglycemia, and a close relationship between paired YSI and ACE concentrations from common samples. The ACE method identified all nine animals that displayed hypoglycemic distress during the acute phase response to endotoxin injection. The relationship between the YSI analytical method and the ACE monitoring method was found to be nonlinear (YSI = -38.2+13.6.ACE.50; R2 = .99; Sy.x = 7.3 mg/dL), and the use of this equation to predict YSI values from ACE values in an independent data set resulted in linearity when YSI was regressed on the predicted YSI values (YSI = -.78+1.00.Predicted YSI; R2 = .87; Sy.x = 6.9 mg/dL). Even though variation seemed greater for ACE than for YSI, we concluded that a system developed for human self-monitoring of blood glucose, such as the ACE, can be used to monitor the glycemic status of cattle.  相似文献   

3.
A rapid method for determination of progesterone in bovine, goat and porcine plasma as well as in bovine milk was evaluated. The method employed was a solid-phase (125)I radioimmunoassay equipped with progesterone standards in human serum and called the Coat-A-Count procedure. The dilution curves of bovine plasma samples with high progesterone content were parallel with the standard curve based on human serum. The relation between measurements of progesterone levels in bovine plasma using the reference extraction method and the direct Coat-A-Count procedure was highly significant, resulting in the linear regression equation Y = 1.06x-0.04. In case of goat and porcine plasma, the direct method yielded higher results than the reference extraction method (Y = 1.37x + 1.38 and Y = 1.69x - 6.47, respectively). Progesterone concentration in bovine whole milk was much higher when measured by the Coat-A-Count procedure than by the reference Farmos kit (Y = 1.59x + 1.51). However, when the same samples were assayed by a modified Coat-A- Count procedure, i.e. progesterone standards from Farmos kit, the values were more or less identical (Y = 0.88x - 0.21).  相似文献   

4.
Effect of age on liver enzyme activities in serum of healthy quarter horses   总被引：2，自引：0，他引：2  
Serum alkaline phosphatase (ALP), gamma-glutamyl transferase (GGT), 5'nucleotidase (5'NT), sorbitol dehydrogenase (SDH), and aspartate transaminase activities were measured in 10 clinically healthy foals, 10 yearlings, and 10 two-year-old Quarter Horses. Enzyme activities in foals at 0.5 to 3 days, 2 to 3 weeks, and 5 to 7 weeks of age were compared with enzyme activities from yearling and 2-year-old horses. Multivariate analyses of variance revealed significantly higher enzyme values in foals (P less than 0.002). This increase was mainly a result of higher ALP and GGT activities, with lesser effects due to higher SDH and 5'NT activities. Standard deviations for ALP and GGT were also larger in foals than in adult horses. The wide variation of ALP and GGT activities may limit their usefulness in the diagnosis of hepatic disease in foals. Standard deviations for serum AST, SDH, and 5'NT activities were smaller. These enzymes may be indicators of hepatobiliary disease in foals. The high serum enzyme activities in healthy foals may reflect a physiologic difference between foals and adult horses. Relative hepatic mass (as a percentage of body weight) and enzyme activity per gram of hepatic tissue are high in young animals, indicating that the high serum enzyme activities in foals are due partly to a high rate of enzyme production and release.  相似文献   

5.
The Cornell Net Carbohydrate and Protein System (CNCPS) has equations for predicting nutrient requirements, feed intake, and feed utilization over wide variations in cattle (frame size, body condition, and stage of growth), feed carbohydrate and protein fractions and their digestion and passage rates, and environmental conditions. Independent data were used to validate the ability of the CNCPS to predict responses compared to National Research Council (NRC) systems. With DMI in steers, the CNCPS had a 12% lower standard error of the Y estimate (Sy.x) and three percentage units less bias than the NRC system. For DMI in heifers, both systems had a similar Sy.x but the NRC had four percentage units less bias. With lactating dairy cows' DMI, the CNCPS had a 12% lower Sy.x. Observed NEm requirement averaged 5% under NRC and 6% under CNCPS predicted values at temperatures above 9 degrees C but were 18% over NRC and 9% under CNCPS at temperatures under 9 degrees C. Energy retained was predicted with an R2 of .80 and .95 and a bias of 8 and 4% for the NRC and CNCPS, respectively. Protein retained was predicted with an R2 of .75 and .85 with a bias of 0 and -1% for NRC and CNCPS, respectively. Biases due to frame size, implant, or NEg were small. Body condition scores predicted body fat percentage in dairy cows with an R2 of .93 and a Sy.x of 2.35% body fat. The CNCPS predicted metabolizable protein allowable ADG with a bias of 1.6% with a Sy.x of .07 kg compared to values of -30% and .10 kg, respectively for the NRC system.  相似文献   

6.
猪圆环病毒2型间接ELISA抗体检测试剂盒的研制及初步应用   总被引：1，自引：1，他引：0  
以大肠杆菌原核表达系统表达的猪圆环病毒2型Cap蛋白为抗原,建立猪圆环病毒2型间接ELISA检测方法,优化ELISA反应条件,研制猪圆环病毒2型ELISA抗体检测试剂盒。与商品化试剂盒相比,该检测试剂盒敏感性、特异性和符合率分别为95.12%、92.86%和94.55%;同时与猪圆环病毒1型（PCV1）、猪瘟病毒（CSFV）、猪繁殖与呼吸综合征病毒（PRRSV）等多种病毒阳性血清无交叉反应。试剂盒具有较好的重复性,在-20 ℃至少可保存1年以上,将其应用于临床血清样品的检测,结果安徽、广东、广西采样猪场的PCV2阳性率分别为100%、48.39%、100%。  相似文献   

7.
Changes in the intake of dry matter (DM) of the protein-free diet (PFD) fed ad libitum were studied on male rats in relation to the shrunk body mass (SB) and duration of protein-free feeding (t). The intake of DM and changes of SB were investigated on the same rats and during the same experimental periods. The mean intake of DM in relation to PFD feeding periods t = 3, 6, 9, 12, 16 days and the daily DM intake (DMd) in relation to the daily shrunk body mass (SBd) were calculated on logarithmical values according to a model of linear regression y = a + bx and to a model of multiple regression y = b0 + b1x1 + b2x2. The rate of DM intake in relation to the duration of PFD feeding (t) did not differ significantly between age groups (k = 14) but the ak differed significantly. The common coefficient bc = 0.871 +/- 0.012 was less than 1***. This relationship is described by the equation: DM intake = Ak X t0.871, where: DM intake = the sum of intake in the periods of 3, 6, 9, 12 and 16 days (in grams), k = age group, t = PFD feeding period. No significant correlation (P less than 0.05) was found between bk and the initial body mass (SBi) or age of rats (r = -0.21 and -0.02, respectively) but between ak and SBi or age the correlation was highly significant (r = 0.960 and 0.832). This indicates that the amount but not the rate of DM intake depended on the initial body mass or age. The relation between DMd and SBd, the latter increasing with age but decreasing with the duration of PFD feeding, is described by equation: DMd intake = Ad X SBd0.503, where: DMd intake in grams, d = day 1 to 15 of PFD feeding, SBd = daily shrunk body mass in kilograms. The values of Ad decreased with the duration of PFD feeding. The using of multiple regression permitted to describe DMd intake as a function of SBd and (d) by a common equation: DMd intake = 27.02 X SBd0.503 X d-0.103; R = 0.976. Thus the daily DM intake was closely positively correlated with SBd and negatively correlated with the duration of protein-free feeding regardless of the age of rats.(ABSTRACT TRUNCATED AT 400 WORDS)  相似文献   

8.
We studied the pineal gland (PG) growth separating two critical moments of the rat post-natal development: the lactation and post-weaning periods. We studied 30 Wistar rats in the post-natal day - PN day 6, 10, 21, 45, 60 and 90 using light microscopy and quantitative methods (allometry and stereology). We estimated the PG volume (using the Cavalieri's principle) and the number of pineal gland cell nuclei (PGCN, using the disector method). We analysed the correlation of the PG volume (y) versus brain weight (x) in the different age groups (the bivariate study used log-transformed data and the allometric model log y = log a + b log x). The PG growth gradually decelerated in older rats than in younger rats. The major increment of the PG growth was observed between PN day 6 and PN day 10, while the minor increment was observed after weaning between PN day 45 and PN day 60. After 60 days of age differences were no more observed. The relative growth of the PG was allometrically positive in all age groups, and growth curves separated the lactation from the after weaning periods. The number of PGCN of rat continuously increased during post-natal life and differences between the lactation and after weaning periods were significant. It is possible that the supporting cells, fibres and new synapses are responsible for that PG late post-natal increase.  相似文献   

9.
Cyprinid herpesvirus 3 (CyHV-3) is a lethal DNA virus that infects common carp and koi. It has caused outbreak of the disease within both aquaculture and natural environmental ecosystems. However, there is not enough understanding of the distribution of CyHV-3 in the natural environments, partly because there is no suitable quantification method. In this study, we tested CyHV-3 extraction methods from sediment and then compared its abundance between sediment and water using real-time PCR. Sediment samples were taken from lake and pond, and total viral DNA was extracted using the viral elution method recommended by the US Environmental Protection Agency (manual method), as well as a commercial DNA extraction kit for soil (commercial kit method) before PCR detection. 7 of 12 (58%) and 5 of 10 (50%) sediment samples showed PCR positive signal for CyHV-3 DNA using the manual method and the commercial kit, respectively, and consistent results were obtained from the samples using the manual method between two independent primer sets. The quantification of CyHV-3 DNA in natural sediment using the manual method and external standard virus revealed that its concentration was 1.2×10(4) to 3.3×10(5) copies DNA/kg. The concentration in sediments was 46-1238 times higher than that in water from the same location, suggesting that sediment could act as a reservoir for CyHV-3 in natural freshwater environments. This is the first report of the existence of CyHV-3 in the sediment of a natural lake or pond.  相似文献   

10.
An enzymatic, kinetic method for determining serum lipase activity was evaluated and compared to a standard manual method for use in dogs. The kinetic method was a commercial kit adapted for use on a tandem access clinical chemistry analyzer and utilized a series of coupled enzymatic reactions based on the hydrolysis of 1,2-diglyceride by lipase. The manual method was the Cherry-Crandall technique based on the titration of base against the acid formed by hydrolysis of an olive oil substrate by lipase. The correlation between the two methods was very good (r = 0.94). The reference range for 56 clinically healthy dogs assayed by the kinetic method was 90 to 527 U/L. Diseases associated with a greater than twofold elevation in serum lipase activity as determined by the kinetic method included pancreatitis, gastritis with liver disease, and oliguric renal failure with metabolic acidosis. In some cases, pancreatitis was seen with other clinical problems, such as gastroenteritis, diabetic ketoacidosis, duodenal mass, disseminated intravascular coagulation, and septic peritonitis. Diseases associated with serum lipase activity within the reference range or elevated less than twofold included gastritis, gastric ulcer, cholestasis, phenobarbital-induced hepatopathy, colitis, copper hepatopathy, abdominal hematoma, apocrine gland adenocarcinoma, and thrombocytopenia with pneumonia.  相似文献   

11.
An inexpensive and easily automated flow injection method for determination of urea in cow’s milk was evaluated. Urea is hydrolysed by urease and in a gas diffusion cell the ammonia formed passes a membrane into an indicator solution. The resulting colour change of the indicator is measured at 590 nm.The repeatability of the analysis, expressed as the coefficient of variation (C.V.), was between 0.5 and 1.2%. Measured (y) and expected (x) milk urea concentrations after addition of known amounts of urea were related according to the equation y = 1.00× – 0.12 with a C.V. for the regression of 1.8%. Recommended amounts (0.02 %) of the preservative bronopol (2-bromo-2-nitropropane-1,3-diol) added to the milk did not affect the results (P > 0.05).  相似文献   

12.
本研究旨在研制一种牛血清淀粉样蛋白A（SAA）时间分辨荧光免疫层析定量检测试剂盒,用于牛奶中SAA含量的临床快速检测。采用双抗体夹心法结合荧光免疫层析技术,在结合垫上固定荧光微球标记的抗SAA单克隆抗体及荧光微球标记的鸡IgY的混合物,在硝酸纤维素膜的检测区包被另一株抗SAA单克隆抗体,在硝酸纤维素膜的质控区包被山羊抗鸡IgY。经抗体原料筛选及荧光微球标记抗体的工艺优化后,绘制标准曲线并对试剂盒的空白限、精密度、稳定性及样本测试性能进行初步评估。结果显示,Medix SAA-2单克隆抗体包被与YBX SAA-3单克隆抗体标记为最适抗体配对原料。荧光微球标记抗体的工艺中,荧光微球与抗体的质量投料比为40∶1、偶联剂与荧光微球羧基摩尔比为2∶1的条件为最优组合。试剂盒标准曲线的四参数拟合曲线方程为y=（1.03947-0.00182）/[1＋（x/12.08222）×（-0.84692）]＋0.00182,线性相关系数R2=0.9997。研制的牛SAA检测试剂盒空白限为0.052 mg/L。精密度测试结果显示,批内变异系数 < 15%,批间变异系数 < 20%。室温稳定性试验表明,试剂盒在室温密封存放6个月的荧光T/C值相对跌幅约15%。自制试剂盒与上海蓝基试剂盒的样本对比测试相关系数R2为0.97。综上所述,本试验研制的试剂盒具有操作简便、灵敏度高、成本低廉等优点,能满足临床测定需求,可作为一种新型牛SAA检测的快捷、准确的检测手段。  相似文献   

13.
The Long-Evans Cinnamon (LEC) mutant rat shows higher incidence of renal cell carcinomas induced by a treatment with the chemical carcinogen N-diethylnitrosamine, as compared to the normal control rat. We performed the first genome-wide scan for genes responsible for susceptibility to chemically induced renal cell carcinoma in an F2 intercross obtained by mating the LEC and Fischer-344 (F344) rats. The genotype of 71 (F344 x LEC) F2 progenies was determined with the use of 338 simple sequence length polymorphisms (SSLPs) spread over the genome. The F2 rats which carried renal cell carcinoma were shown to possess the incidence of homozygosity of the LEC allele which is higher than that of the other genotypes at SSLP markers on chromosome 5 (chi2 = 17.5 for D5Rat21). Our linkage analysis has led to the revelation of a novel gene that influences susceptibility to renal cell carcinoma on rat chromosome 5.  相似文献   

14.
Background: The rat is used often to assess the toxicity of new chemical entities in preclinical drug development. Bilirubin concentration in rat serum is routinely determined by colorimetric methods, but false positive results due to hemolyzed serum or direct interferences by test compounds may occur. Capillary electrophoresis (CE) is an automated method that requires small sample volume and facilitates the direct detection of bilirubin. Objective: The purpose of this study was to evaluate a CE method for detecting bilirubin and albumin‐bound bilirubin in rat serum and to measure potential interference by hemolysis and specific test compounds. Methods: Serum samples from male Sprague Dawley rats (n=20) were used in the study. Results obtained on a Beckman P/ACE MDQ CE instrument equipped with a UV‐detector were compared with those obtained using a colorimetric method on a Hitachi 912 analyzer. Bilirubin standards were used to evaluate the detection and stability of bilirubin in rat serum, and vials with ultrafiltration membranes were used to separate albumin‐bound bilirubin. Intraday and interday coefficients of variation (CV), linearity, and the effects of added hemoglobin and a test compound on CE results were determined. Results: The CE method was capable of detecting bilirubin and albumin‐bound bilirubin in rat serum samples with reproducible results and good accuracy. CVs were <3% and linearity of the CE assay was high (R2=0.9951). Abnormally high bilirubin peaks due to the presence of hemoglobin or the test compound were easily distinguished by means of CE. Conclusion: CE is a good alternative to the colorimetric methods currently used for the determination of bilirubin in rat serum.  相似文献   

15.
An automated colorimetric method for determining lipase activity in canine sera was evaluated for precision, linearity and correlation to existing assay methods. The colorimetric method was a commercial reagent that used a series of enzymatic reactions based on the hydrolysis of 1,2 diglyceride by pancreatic lipase. Within-run and between-run coefficients of variation were < 6.8% and < 8.3%, respectively. Linearity was determined to be at least 1366 U/L. Canine serum lipase concentrations attained using the colorimetric method were compared to both titrimetric and dry-film methods for measuring serum lipase activity, resulting in significant (P < or = 0.05) correlation coefficients of 0.92 and 0.77, respectively. Canine serum lipase concentrations measured using the colorimetric assay on 2 different automated analyzers had a significant (P < or = 0.05) correlation coefficient of 0.92. A laboratory reference range using serum samples from 56 healthy dogs (0-561 U/L) was established. There were no significant (P < or = 0.05) differences in mean serum lipase concentrations comparing male and female dogs or comparing young dogs (< or = 3 y) to mature (4-7 y) and older (> 7 y) dogs using this assay. It was concluded that the automated colorimetric assay was a reliable indicator of canine serum lipase activity and offered several advantages, including small sample volume and short analysis time.  相似文献   

16.
为准确测定婴幼儿配方乳粉中的磷含量,对测定方法的最佳实验条件、精密度、稳定性、重现性及回收率进行研究.结果发现采用可见分光光度法测定婴幼儿配方乳粉中的磷含量,重现性好,准确度高,建立的线性方程为y=0.0372x+ 0.0039(R2=0.9997),方法的平均回收率为98.5％、RSD值为0.39％.随机抽取市售的30批次婴幼儿配方乳粉进行检测,发现不同阶段的乳粉磷含量不同,含量顺序为幼儿配方乳粉＞较大婴儿配方乳粉＞婴儿配方乳粉,具体值分别为(448±56)、(382±59)、(250±58)mg/g,不同品牌同一阶段的乳粉磷含量也存在较大差异.  相似文献   

17.
Blood glutathione peroxidase (GSH-Px) levels in 709 normal dromedary camels (442 females and 267 males) were assessed in the Canary Islands. All animals were intensively reared, and three different nutritional systems were evaluated, depending on selenium content of the diet. Mean GSH-Px level in the total population was 288.5+/-157.2 IU x g(-1) Hb. Reference ranges were estimated and enzymatic activities below 51 IU x g(-1) Hb were considered inadequate. GSH-Px activities obtained in females (298.1+/-155.7 IU x g(-1) Hb) were significantly (P = 0.037) higher than in males (272.6+/-157.2 IU x g(-1) Hb). When age groups were compared, only males between 6 and 12 months old exhibited significantly lower mean GSH-Px (P = 0.006) than females. A high correlation (r = 0.88) between serum selenium concentration and blood GSH-Px activity was estimated, and the regression equation was y = 2.5101x + 42.423. Selenium content of the diet above 0.1 mg x kg(-1) DM seems to supply adequate selenium requirements for dromedaries under intensive husbandry.  相似文献   

18.
A Baker 9000 hematology analyzer (electronic impedance) was purchased to replace an Ortho ELT-8/ds analyzer (laser optics) due to discontinued technical support. An analytical comparison of hemograms from healthy dogs, rats, and mice was made from paired disodium ethylenediamine tetra-acetate anticoagulated blood samples. Both instruments were calibrated with human blood products, and the ELT-8/ds hematocrit (HCT) was calibrated to a spun packed cell volume (PCV) for each species. For Beagle dogs (n = 49), Baker 9000 mean platelet (PCV) counts had a negative bias of -89 X 10(3)/microliter when compared to ELT-8/ds values. Mean +/- standard error manual PLT counts compared well with Baker 9OOO values for dogs (n = 10): 369 +/- 28 vs. 367 +/- 27 X 10(3)/microliter; r = 0.93. For CD-1 mice (n = 44), Baker 9000 mean white blood cell (WBC) counts had positive biases of 1. 1 X 10(3)/microliter when compared to ELT-8/ds and 0.5 X 10(3)/microliter when compared to hemacytometer counts. Diluted microsamples using the predilution mode on the Baker 9000 compared well with undiluted samples for mice. For Sprague-Dawley rats (n = 70), Baker 9000 mean WBC, red blood cell (RBC), and PLT counts had absolute biases of 0.8 X 10(3)/microliter, -1.09 X 10(6)/microliter, and -357 X 10(3)/microliter, respectively, when compared to ELT-8/ds values. Baker 9000 RBC, WBC, and PLT counts from rats compared well with reference hemacytometer counts. The Baker 9000 HCT determination for rats had an absolute negative bias of 6% when compared to the ELT-8/ds values or spun PCV. The Baker 9000 required whole blood calibration to PCV for accurate determination of HCT for rats. The biases between analyzers may be due to inherent physical differences between the analytical methods and/or the calibration techniques.  相似文献   

19.
The importance of blood and colostrum/milk serum gamma-glutamyl transferase (gamma-GT) enzyme activity was evaluated to assess passive transfer status in healthy lambs. Thirty Akkaraman sheep (3-6 years old) were used which had normal pregnancy period and the same conditions, and the age of the lambs ranged between 0 and 15 days. Blood and colostrum/milk samples were collected from sheep and lambs after birth, before suckling (0) and after on 1st, 3rd, 7th and 15th days. Serum immunoglobulin G (IgG) concentration was determined by the use of Single Radial Immunodiffusion method. Serum gamma-GT activity was measured, using a commercially available kit in blood and colostrum/milk samples. Correlations were carried out between immunoglobulin and gamma-GT levels. Regression models (simple and multiple) were calculated with significant data. Linear correlation was determined between colostrum/milk gamma-GT activity and IgG concentrations and between serum gamma-GT activity and IgG concentrations in lambs on the 0 day. (r: 0.607, P: 0.001), 1st (r: 0.768, P: 0.001) and the 3rd (r: 0.603, P: 0.001) days and on the 1st (r: 0.637, P: 0.001) and 3rd (r: 0.478, P: 0.012) days in the experiment, respectively. Multivariate regression models were developed to estimate sample IgG concentration. Serum and colostrum/milk IgG concentration could be predicted using the formula: lamb serum IgG = 825 + 0.688 (lamb gamma-GT) + 52 (days); colostrum/milk IgG = 832 + 0.505 (colostrum/milk gamma-GT) - 167 (days). The regression models were moderately accurate in predicting serum IgG concentration (R2 = 0.51) and colostrum/milk IgG concentration (R2 = 0.55). Test sensitivity and positive predictive values for serum gamma-GT enzyme activity were found to be 96 and 100% and for colostrum/milk gamma-GT enzyme activity were found to be 100 and 68% to prediction IgG concentration. Serum and colostrum/milk gamma-GT activity can be used to assess passive transfer status of lambs. Along with this, regression models used to calculate serum and colostrum/milk gamma-GT activities found to be useful to estimate sample IgG concentration. The use of serum and colostrum/milk gamma-GT enzyme activity was found useful especially after birth on the 0, 1st and 3rd days.  相似文献   

20.
In the present study the osteoclast activity was monitored longitudinally in porcine blood samples by measuring the tartrate-resistant acidic phosphatase (TRAP) activity with several methods described for human samples. These methods differed in their specificity for bone-specific TRAP and in their practicability. The validity of TRAP measurements was evaluated by comparison with the peripheral concentrations of the N-terminal fragments of type I collagen with attached cross-links (NTx), a highly bone-specific parameter of bone collagen degradation, using a commercially available test kit developed for human samples. On selected days urine samples were collected for the determination of pyridinium cross-links. The determinations of cross-links in urine were normalized for the creatinine concentrations. However, they were not related to fluoride-sensitive TRAP (fsTRAP) and NTx measurements in serum. The fsTRAP activity in serum, which is assumed to be highly bone-specific, was highly correlated with the NTx concentrations in serum under different experimental conditions. As measurements in blood may be more easily standardized than those in urine, fsTRAP measurements in serum seem to be a highly practicable method to characterize osteoclastic activity in the pig.  相似文献   

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