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1.
Alkaline phosphatase (ALP) isoenzyme analysis, using a combination of wheat germ lectin (WGL) precipitation, levamisole inhibition and an automated p-nitrophenylphosphate assay was validated for use with serum from monkeys (Macaca fascicularis) and used to determine the activities of liver ALP (LALP), bone ALP (BALP) and intestinal ALP (IALP). Based on serial dilution studies and within-run and between-run coefficients of variation, each assay had excellent linearity and acceptable precision. In addition, liver and intestinal mucosa extracts for tissue specific alkaline phosphatases were used to confirm assay validations. Gender-specific differences for total ALP, LALP, and BALP activities were present in sera from normal monkeys between 2 and 4 years of age. Males had 1.3-fold higher total ALP and LALP activities, and 1.5-fold higher BALP activity compared with females. The majority of ALP activity in normal monkey serum was LALP isoenzyme activity, which ranged from 56.7% to 94.7% of total activity. Serum BALP activity ranged from 5.3% to 42.8%. There was negligible IALP activity in all serum samples.  相似文献   

2.
Serum alkaline phosphatase (ALP) activities were measured during dry and lactational periods to investigate the influence of lactation on serum ALP activity in cows. Higher levels of serum ALP activity were seen in lactational periods than in dry periods. The serum activities of bone-specific ALP (BALP), liver ALP (LALP), tartrate resistant acid phosphatase (TRAP) and aspartate aminotransferase also increased in lactational periods. ALP activities in the bone extract and in whey were decreased at similar rates by the addition of lectin. Moreover, since the ALP band in whey was observed to have the same migration in polyacrylamide gel (PAG) disk electrophoresis as that of the bone extract, analysis of ALP isoenzymes by lectin affinity or PAG disk electrophoresis could not distinguish ALP originating from the mammary gland from that of bone. In this study, it was clear that the increased level of serum ALP activity was due to increases of BALP and LALP in lactational periods. However, the extent of the influence of ALP originating from the mammary glands on serum ALP activity was unknown. Judging from changes of BALP and TRAP activities in the serum and the correlation between the both, it was guessed that ALP originating from the mammary glands influenced serum ALP activity.  相似文献   

3.
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4.
Serum alkaline phosphatase (ALP) isoenzymes were studied in normal dogs using a commercially available polyacrylamide gel disk electrophoresis kit (PAG/disk kit). Serum samples taken from the dogs were incubated with neuraminidase, after which most showed ALP isoenzymes as two characteristic stained bands. To determine the origin of each band, ALP isoenzymes of serum and tissue extracts (liver, intestine and bone) were characterized by heating, wheat germ agglutinin (WGA) and levamisole treatments. The results suggested that the band detected on the anode was liver ALP (LALP) and that the band detected on the cathode represented bone ALP (BALP), and both were corticosteroid-induced ALP (CALP). The percentage of each ALP isoenzyme to total ALP activity was estimated by densitometry. The percentage of BALP was the highest in young dogs (age<1 year, 64.7% ), and this value decreased with age. In contrast, the percentage of LALP in young dogs (22.2%) was much lower than that in middle-aged dogs (ages 1 year to 7 years, 59.3%) and old dogs (ages>7 years, 50.4%). The present results suggested that a commercially available PAG/disk kit is capable of detecting three serum ALP isoenzymes in dogs, and further that it may have clinical applications in the evaluation of ALP isoenzymes in veterinary medicine.  相似文献   

5.
BACKGROUND: Increased serum activity of total alkaline phosphatase (TALP) has been found in dogs with mammary neoplasms, especially malignant mixed tumors. We hypothesized that the bone isoenzyme of alkaline phosphatase (BALP), a specific indicator of osteoblastic activity and bone formation, may contribute to increased TALP in dogs with mammary neoplasms with osseous transformation. OBJECTIVE: The purpose of this study was to compare serum TALP, BALP, and other ALP isoenzyme activities in dogs with mammary malignant neoplasms with and without osseous transformation. METHODS: Twenty-one female dogs with malignant mammary neoplasms were compared with 21 clinically healthy, age-matched female control dogs. Physical, clinicopathologic (including preprandial and postprandial serum bile acids, ACTH stimulation, and low-dose dexamethasone suppression tests), radiographic, and ultrasonographic examinations were performed on all dogs with tumors to assess coexisting conditions. On the basis of histologic examination of excised tumors, dogs were further classified as having epithelial (n = 11) or mesenchymal/mixed (epithelial-mesenchymal) (n = 10) neoplasms, the latter of which had histologic and radiologic evidence of bone formation. Serum TALP, BALP, liver alkaline phosphatase (LALP), and corticosteroid-induced alkaline phosphatase (CALP) activities were measured using biochemical methods. RESULTS: Dogs with malignant mammary tumors had significantly higher (P < .05) median serum TALP (170 U/L), BALP (59 U/L), LALP (49 U/L), and CALP (24 U/L) activities, compared with control dogs (81, 32, 37, and 5 U/L, respectively). Significantly higher activities of BALP and LALP were found in dogs with epithelial neoplasms; whereas, only CALP activity was higher in dogs with mesenchymal/mixed neoplasms. There was no significant difference in TALP or isoenzyme activitities between epithelial and mesenchymal/mixed groups. CONCLUSION: BALP activity is increased in some dogs with malignant mammary tumors but does not account for the increase in TALP in dogs with neoplasms that have osseous transformation.  相似文献   

6.
The concentration of serum alkaline phosphatase (SALP) is commonly elevated in hyperthyroid cats. Agarose gel electrophoresis, in tris -barbital-sodium barbital buffer, with and without the separation enhancer neuraminidase, was used to investigate the sources of the constituent isoenzymes of SALP in serum samples from 34 hyperthyroid cats, comparing them to sera from five healthy cats and to tissue homogenates from liver, kidney, bone and duodenum. Contrary to previous reports, treatment of serum with neuraminidase made differentiation of the various isoenzymes more difficult to achieve. A single band corresponding to the liver isoenzyme (LALP) was found in 100 per cent of healthy cats. Eighty-eight per cent of the hyperthyroid cats showed two bands, corresponding to the liver and bone (BALP) isoenzymes while 12 per cent showed a LALP band alone. In hyperthyroid cats, there was a significant correlation between the serum L-thyroxine concentrations and the SALP concentrations. These findings suggest pathological changes in both bone and liver in most cases of feline thyrotoxicosis.  相似文献   

7.
Sixty-one dogs with appendicular osteosarcoma were treated with amputation and chemotherapy of cisplatin and doxorubicin. Serum samples were obtained before and after treatment for determination of total alkaline phosphatase (TALP) activity as well as the activities of the constituent bone (BALP), liver (LALP), and corticosteroid-induced (CALP) isoenzymes. The relationship between alkaline phosphatase activities and survival was examined by Cox proportional hazards regression analysis and Kaplan-Meier log rank analysis. Mean activity of TALP, BALP, and LALP decreased significantly after treatment (P < .001). TALP and LALP activities before treatment were significantly correlated with survival (P = .006 and .001, respectively). The correlation between BALP activity before treatment and survival approached significance (P = .054). CALP activity and TALP, BALP, and LALP activities after treatment were not significantly correlated with survival. Dogs with normal pretreatment TALP and BALP activities survived significantly longer than dogs with increased pretreatment activities (P = .001 and .003, respectively). Median survival times for dogs with normal or increased TALP activities before treatment were 12.5 and 5.5 months, respectively; and median survival times for dogs with normal or increased BALP activities before treatment were 16.6 and 9.5 months, respectively. In the design of future clinical trials involving dogs with osteosarcoma, consideration should be given to stratifying the randomization according to alkaline phosphatase activity. In addition, alkaline phosphatase activity should be a factor considered by clinicians attempting to tailor the aggressiveness of adjuvant chemotherapy to the needs of individual patients or owners.  相似文献   

8.
Serum bone specific alkaline phosphatase (BALP) and osteocalcin were measured in 9 Thoroughbred and 4 Quarter Horse (QH) foals. Eight were colts, and 5 were fillies. The first blood sample was collected from foals between 10 and 14 hours after birth on day 1. Blood then was collected on days 3, 6, 9, 12, 15, 18, 21, 28, 35, 42, 49, 56, 70, 84, 98, and 112 between 7:00 and 9:00 am. Serum bone metabolism marker raw data were analyzed with analysis of variance with repeated measures over time with gender and breed in the model. Average serum osteocalcin concentrations were higher for Thoroughbred than QH foals: 152.1 ± 4.6 ng/mL and 131.3 ± 6.3 ng/mL (mean ± standard error), respectively (P = .01). No overall differences were seen for gender (P = .10). However, on day 1, colts had higher osteocalcin than did fillies at 199.6 ± 30.2 ng/mL and 93.8 ± 32.4 ng/mL, respectively (P = .04). Thoroughbred foals had higher average serum BALP concentrations than did QH foals, with average values of 260.8 ± 13.4 U/L and 205.1 ± 18.5 U/L, respectively (P = .02). No gender differences were seen for serum BALP (P = .48). Serum carboxy-terminal propeptide of Type I procollagen (PICP) concentrations could not be measured in this study because the Metra Biosystems assay for PICP could not be validated.

Introduction

Bone synthesis by the osteoblast can be divided into 3 phases: proliferation, matrix development and maturation, and mineralization.1 Gene expression of type I collagen takes place during the proliferation of the osteoblast cells. The expression of bone specific alkaline phosphatase (BALP) reaches its maximum during matrix maturation and declines as matrix mineralization starts. The osteocalcin gene is expressed during matrix mineralization.When type I collagen is produced as procollagen and released into the extracellular space, the amino and carboxyterminal propeptides of type I procollagen (PINP and PICP, respectively) are cleaved off.2 Serum PICP has been shown to be a good marker for bone formation in metabolic bone diseases.3 In Thoroughbred fillies, PICP has an inverse relationship with age, with highest values found in animals less than 1 year of age.4 Serum alkaline phosphatase (ALP) has been measured in the young foal and is highest at birth, decreasing to a constant level by 2 months of age.5, 6 and 7 Serum BALP constitutes 60% to 92% of the total serum ALP in the horse and is highest in the foal.4 and 8 As the foal matures, there is an inverse relationship between age and serum BALP.4 and 9 Serum osteocalcin in foals less than 6 months of age has not been reported as having the same age-related pattern as serum BALP.10However, younger horses have higher serum osteocalcin values than mature horses.11, 12 and 13 Davicco et al14 showed plasma osteocalcin age-related changes for Thoroughbred foals with radioimmunoassay (RIA). Plasma osteocalcin was low at birth, increased to day 8, and then dropped to day 15. The objective of this study was to establish normal ranges and age-related changes in serum BALP, PICP, and osteocalcin in the foal with enzyme-linked immunospecific assays (ELISAs).

Materials and methods

Four Quarter Horse (QH; 2 fillies and 2 colts) and 9 Thoroughbred (3 fillies and 6 colts) foals were included in the study from birth through 112 days of age. Foals were born from February 5 to May 13, 1998. Mares and foals were housed on 40 acres of Bahiagrass (Paspalum notatum) pasture and fed a 15% crude protein (as fed) sweet feed. Body scores were recorded every 28 days on a scale from 1 to 9.15 Concentrate was fed to each mare at 1.5 kg/100 kg body weight daily and was increased by 20% for each body condition score below 5 and decreased by 20% for each body condition score above 5. Mares were individually fed in 3.6 × 3.6—m stalls twice daily, with foals allowed access to the mares feed. Trace mineral salt blocks were available in the pastures. Water was available at all times.Blood was collected from foals between 10 and 14 hours after birth on day 1. Blood then was collected on days 3, 6, 9, 12, 15, 18, 21, 28, 35, 42, 49, 56, 70, 84, 98, and 112 after morning feedings. Except for day 1, all blood samples were collected between 7:00 and 9:00 am. All blood samples were collected with jugular venipuncture into a glass vacutainer containing no additives or anticoagulants and were allowed to clot. Serum was separated and frozen at −20°C within 4 hours of collection. All samples were analyzed within 6 months of collection.The Alkphase-B immunoassay for the determination of BALP (Metra Biosystems, Mountainview, Calif) and the NovoCalcin immunoassay for determination of osteocalcin (Metra Biosystems), used in this study, have been previously validated in the horse.16 and 17 The Prolagen-C immunoassy for determination of the PICP (Metra Biosystems) has not been previously validated in the horse.17Serum bone metabolism marker raw data were analyzed with analysis of variance with repeated measures over time with gender and breed in the model. Analyses were performed with Statistical Analysis System with proc glm for the analysis of variances.18

Results

Average serum osteocalcin concentration for the testing period was higher for Thoroughbred than QH foals: 152.1 ± 4.6 and 131.3 ± 6.3 ng/mL (mean ± standard error), respectively (P = .01). No overall differences were seen for gender (P = .10). However, on day 1, colts had higher osteocalcin concentrations than did fillies at 199.6 ± 30.2 ng/mL and 93.8 ± 32.4 ng/mL (P = .04; Fig 1).
Full-size image (4K)
Fig. 1. Serum osteocalcin (OC) over time (mean ± standard error). A, Changes over time between breeds. B, Changes over time between gender. P < .05.
The intraassay coefficient of variation (CV) was 2.3%, 4.4%, and 10.3% for 4.7, 20.7, and 159.4 ng/mL osteocalcin serum pools. Interassay CV was 5.4%, 4.8%, and 6.1% for 2.3, 6.4, and 24.1 ng/mL osteocalcin serum pools.Thoroughbred foals had higher average serum BALP concentrations than did QH foals, with average values of 260.8 ± 13.4 U/L and 205.1 ± 18.5 U/L, respectively (P = .02). Daily serum BALP breed differences were detected only on days 12 and 112, with Thoroughbred foals having higher values than QH foals at 240.4 ± 18.4 U/L versus 168.6 ± 24.2 U/L (P = .05) and 172.3 ± 14.3 U/L versus 107.6 ± 23.2 U/L (P = .05; Fig 2).
Full-size image (4K)
Fig. 2. Serum BALP over time (mean ± standard error). A, Changes over time between breeds. B, Changes over time between genders. P < .05.
No gender differences were seen (P = .48; Fig 2). The intraassay CV was 3.6%, 2.8%, and 4.7% for the 51.9, 139.4, and 401.8 U/L BALP serum pools. Interassay CV was 5.78%, 11.8%, and 13.7% for the 15.8, 71.3, and 145.6 U/L BALP serum pools.The Prolagen-C immunoassay procedure for the determination of PICP used in this study could not be validated. Linearity for serial dilutions of serum samples could not be shown. Therefore, no PICP data are shown.

Discussion

Early age-related changes in plasma osteocalcin have been previously reported for the foal with RIA.14 Plasma osteocalcin levels were low at birth, increased to day 8, and then dropped to day 15. This study supports those trends in plasma levels of osteocalcin. However, as Hoyt and Siciliano16 observed, serum osteocalcin values determined with the immunoassay (Metra Biosystems) were higher than those observed with RIA. The antibody specificities may be different between the 2 assays. Thoroughbred foals had higher average serum osteocalcin than QH foals, which supports findings that serum osteocalcin differs among breeds.19 No gender differences had previously been reported for serum osteocalcin in horses of different ages, but when foals are stressed by weaning or exercise, gender differences were seen.12 and 20 Although no overall gender differences were seen in this study, on day 1, colts had higher serum osteocalcin than fillies. Plasma cortisol is high in the newborn foal.21 Although no serum cortisol was measured in this study, there may be different levels of cortisol or different responses to cortisol between the colts and fillies as a result of foaling. Because glucocorticoid administration results in suppressed serum osteocalcin in the horse,22 it would be of great value to understand the relationship between gender and cortisol in the neonatal foal.Serum BALP (making up most of serum ALP) values in the neonatal foal, extensively documented in this study, are in agreement with the measurements of serum ALP established in earlier reports.5, 6 and 7 Serum BALP is high at birth and decreases to a lower level by 2 months of age. Average serum BALP is higher in Thoroughbred foals than QH foals, and there are no gender serum BALP differences. No other reports for breed or gender differences concerning serum BALP in the horse have been documented. Likewise, in newborn humans, no serum BALP gender differences have been observed for the first 10 weeks of life.23Price24 and Jackson et al9 used the radioimmunoassay provided by Orion Diagnostica to determine PICP concentrations.4 and 9 Because the Metra Biosystems PICP procedure could not be validated in this study, no comparison with reported data could be made.

Conclusion

Serum BALP and osteocalcin concentrations were measured during the first 112 days of age with age, gender, and breed ranges for the foals being established when ELISA assays are used (Metra Biosystems). Because the total number of animals was small and variability of the data was large, the statistical power to detect meaningful differences for gender and breed was small. However, the data presented show trends of serum bone formation markers, some statistical differences for gender and breed, and variability of the foal during the first 112 days of age. In agreement with Price,24 a single measurement of a serum bone metabolism marker is of little clinical value, especially for the young foal where the variability is high. Because RIA ranges are typically lower than with ELISA assays for serum osteocalcin, the type of assay used should be considered when comparing serum osteocalcin levels between experiments. For use of serum markers to assess bone metabolism in the foal, the relationship of these markers with foal maturation, endocrinology, and skeletal growth needs to be resolved.  相似文献   

9.
Dogs received either 4 mg/kg of prednisone or sterile saline daily for 32 days. Serum samples were assayed every 4 days for total alkaline phosphatase (ALP) and corticosteroid-induced ALP isoenzyme (CIALP) activity. The initial and major increase of serum ALP was attributed to the liver isoenzyme of ALP (LALP), however, CIALP began to increase by day 8 and was significantly increased by day 24. Prior to treatment and on day 32, sections of liver from control and prednisone-treated dogs were stained for ALP activity after blocking the staining activity of LALP with levamisole. The staining activity of CIALP was compared to the staining activity of LALP in liver sections from control dogs and from dogs in which the bile duct was ligated. It was determined that CIALP was located in that area of the hepatocyte membranes which comprise the bile canaliculi.  相似文献   

10.
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11.
BACKGROUND: Assessment of bone formation activity is an important component of pharmacologic efficacy and toxicity evaluations for compounds in development for osteoporosis therapies. Antemortem biomarkers of bone formation and remodeling in rodents are uncommon. While the periosteal alkaline phosphatase (ALP) assay is a postmortem and laborious means of testing bone-building activity, the semiautomated ALP isoenzyme assay is an antemortem assay that is performed on an automated chemistry analyzer after 2 simple dilutions of the initial serum sample and a short incubation. OBJECTIVES: The goal of our investigation was to determine if the serum bone ALP (BALP) data obtained from the semiautomated ALP isoenzyme assay had a similar pattern of response when compared with the periosteal ALP (PALP) assay for use in pharmacologic screening in rats. METHODS: Serum and bone tissue samples were obtained from orchidectomized Wistar rats, a model of clinically induced osteoporosis. Subsequent bone formation was initiated via treatment with one of several compounds. In study 1, orchidectomized male rats were given either vehicle, dihydrotestosterone or a testosterone derivative subcutaneously every 4 days for 28 days. In study 2, orchidectomized male rats were given either vehicle or compounds A, B, or C by oral gavage daily for 15 days. Blood and tibias were collected at necropsy. Serum was analyzed for BALP activity using a semiautomated ALP assay. Tibias from the same rats were analyzed for PALP activity. RESULTS: Serum BALP activity paralleled PALP activity within each group when compared with the controls. CONCLUSION: Our data indicate that the semiautomated serum BALP isoenzyme assay may be used as a biomarker of bone-building potential in rat models of osteoporosis. This assay affords many advantages to investigators of musculoskeletal diseases, including the potential to measure multiple data points in a single study.  相似文献   

12.
Cats with hyperthyroidism [(increased serum thyroxine (T(4))] commonly have increased serum alkaline phosphatase (ALP) activity in addition to other serum biochemical abnormalities. Serum biochemical profiles were obtained from 10 hyperthyroid cats which had increased serum ALP. Agarose gel electrophoresis of serum from these cats was performed and stained for alkaline phosphatase activity. Alkaline phosphatase activity was calculated for each of the separate bands obtained, and the results were compared to those of tissue extracts, serum from normal cats, and serum from normothyroid cats with increased serum ALP activity. The hyperthyroid cats had increased ALP activity in bands corresponding to isoenzymes originating in the liver, bone, and an unidentified tissue source.  相似文献   

13.
Total serum alkaline phosphatase (ALP) activity is the product of the combined activity of isoenzymes from a number of tissue sources. In this study, a commercially available kit for electrophoretic separation of ALP isoenzymes in an agarose gel was used to separate ALP isoenzymes in feline tissue extracts and serum. Five separate bands of ALP activity were identified. These bands were numbered 1 to 5 with band 1 having the most anodal migration. The tissue of origin corresponding to the migration position of the isoenzymes are as follows: Band 3 was the liver isoenzyme, band 4 was the bone isoenzyme and ALP isoenzymes of both intestine and kidney migrate in the position labelled band 5. Band 1 appears to be related to albumin and does not represent true ALP activity. The tissue source of band 2 (a and b) was not identified. Serum ALP activity of mature, healthy cats is primarily of liver origin. Immature cats (< 1 year of age) have a greater proportion of the bone isoenzyme in the serum.  相似文献   

14.
The main purpose of this study was to ascertain whether isoelectric point determination of alkaline phosphatase (AP) using an isoelectric focusing technique on agarose gels could define the isoenzymes present in healthy equine serum. The isoelectric points of AP extracted from nine tissues ranged from pH 3.5 to 7.5 with all tissues having multiple bands. There was considerable similarity in band pattern among tissues, with only pancreatic and colostral AP having substantially different isoelectric points from the others. Sera contained thirteen bands with isoelectric points ranging from pH 3.5 to 6.2 and as each band was common to more than one tissue it was not possible to define the tissue origin of these by direct comparison with tissue patterns. The intensity of all serum bands declined as foals aged, with the greatest decrease in bands 4 and 5 (numbered from the anode). There was no relative change in the banding pattern between early and late pregnant mares or in the sera of two foals before and after ingestion of colostrum. The mean (+/- SD) total serum AP activities of young foals (1676 +/- 1100 IU/L), three month foals (402 +/- 64 IU/L) early pregnant (190 +/- 54 IU/L) and late pregnant mares (109 +/- 26 IU/L) were significantly different from each other whereas colostral ingestion in two neonatal foals had no effect. We concluded that equine AP is a very heterogeneous protein and that normal horse sera do not contain significant renal or small intestinal derived AP. However isoelectric focusing alone could not differentiate bone from liver derived AP in sera.  相似文献   

15.
In mammal circulation, various ferritin-binding proteins (FBPs) are thought to be involved in the clearance of circulating ferritin after complex formation with it. However, horse FBPs are known to cause inhibitory effects on ferritin immunoassay due to the concealment of the ferritin molecule to anti-ferritin antibodies used in the ferritin immunoassay. These inhibitory effects are eliminated by heat treatment of horse serum at 75°C for 15 min. The inhibitory effects on ferritin immunoassay in the sera of ten foal sera (5 females and 5 males) from 1 to 18 months were detected during all periods, and ferritin concentrations of the foal sera increased 20–100% as compared with those of untreated sera by same heat treatment. Ferritin concentrations of heat-treated foal sera increased after birth, reaching to ferritin levels of adult horse at 9 months of age. Thereafter, although serum ferritin concentrations fell down at 12 months of age, these concentrations increased to adult levels at 15 months of age again. The ratio of ferritin concentration of heat-treated serum to that of the untreated serum was regarded as an apparent ferritin-binding activity. Ferritin-binding activities in the sera of foals showed peak at 2 and 4 months of age in females and males, respectively. These results suggested that horse FBPs were heat unstable, and FBPs may play an important role in iron metabolism at early developmental stage.  相似文献   

16.
Flow cytometric assays were used to compare phagocytic and oxidative burst activity of neutrophils from healthy foals less than 7 days of age with the activity of cells from healthy adult horses. The phagocytosis of Staphylococcus aureus by foal neutrophils was less than that observed for adult neutrophils when autologous serum was used as the source of opsonins in the assay. The use of adult serum did not significantly improve the ability of foal neutrophils to attach bacteria. The oxidative burst activity of foal neutrophils was equivalent to that of adult cells. However, when serum or plasma was incorporated into the oxidative burst assay, foal neutrophils demonstrated greatly reduced autofluorescence and a suppressed response to phorbol myristate acetate (PMA), relative to that demonstrated by adult cells. These results suggest that peripheral blood neutrophils from foals have a reduced ability to phagocytose bacteria relative to that exhibited by adult horse neutrophils and that the oxidative burst activity of foal neutrophils is down-regulated in response to an unidentified serum factor(s). Such changes may contribute to the increased susceptibility of foals to septic disease.  相似文献   

17.
Serum alkaline phosphatase activity was found to be increased in 32.6% of equine samples analyzed at the Ontario Veterinary College over an 18 month period. An attempt was made using sensitivity to L-phenylalanine and heat to identify the origin of increased serum alkaline phosphatase isoenzymes present in 44 clinical cases. No difference in sensitivity to either procedure was observed for serum alkaline phosphatase from groups of foals and horses representing different clinical problems. Alkaline phosphatase of osseous tissue origin appeared to be the major source of activity for each group of animals reported.  相似文献   

18.
Bronchoalveolar lavage was performed 5 times, sequentially, on 3 healthy foals while each foal was 6 to 63 days of age. Phagocytosis and bactericidal assays were performed on recovered alveolar macrophages. Corynebacterium equi and alveolar macrophages at a ratio of 10:1 were incubated for 1 hour in medium containing 1% heat-inactivated rabbit anti-C equi serum. After incubation, greater than 90% of the alveolar macrophages contained at least 1 ingested bacterium and each alveolar macrophage contained 9.4 +/- 1.0 bacteria (mean +/- SE). After alveolar macrophages and C equi were incubated for 1 hour in medium containing heat-inactivated pooled normal horse serum, approximately 24% of the alveolar macrophages contained at least 1 bacterium and each alveolar macrophage contained 0.8 +/- 0.7 bacteria. From 6 to 61 days of age, each foal had significantly (P less than 0.05) decreased phagocytic activity by alveolar macrophages, but a significant change in killing of C equi by alveolar macrophages was not found in the foals from 21 to 61 days of age. After incubating alveolar macrophages and C equi for 4 hours in vitro, approximately 75% of ingested C equi remained viable.  相似文献   

19.
Pyogranulomatous pneumonia was induced in Thoroughbred foals by intranasal challenge with freeze-dried cultures of Rhodococcus equi (previously Corynebacterium equi). The incubation period was about 18 days and clinical signs were not seen for a further week. There were marked seasonal and individual foal differences in responses to infection. Elevations in serum caeruloplasmin oxidase activity and copper concentrations appeared to be sensitive indicators of infection. Serum zinc concentrations and serum alpha-mannosidase and alkaline phosphatase activities fell in the more severely infected foals. Use of trace elements and trace element-related parameters along with faecal culture for R. equi could prove useful for early diagnosis of field cases.  相似文献   

20.
Alkaline phosphatase (ALP) isoenzymes obtained from sera of fetus and neonatal calves were examined by electrophoretical analysis using cellulose acetate membrane. A band at Rf 0.45 was detected in the fetal sera. Two bands at Rf 0.53 and Rf 0.31 were observed in the sera of calves 60 days after birth. By immunoelectrophoretical analysis with the anti-kidney ALP in agarose, a precipitin line appeared from the sera of calves at 4.5 hours after birth. No precipitin line was observed from the fetal sera. Results showed that kidney ALP isoenzymes are present in the serum just after birth in cattle.  相似文献   

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