Alkaline Phosphatase In Blood Plasma Research Articles

Preoperative method of assessment of gallbladder lesion in acute cholecystitis

Background. To date acute cholecystitis remains one of the most common urgent abdominal diseases in which postoperative complications and mortality are possible.The aim. To assess the correlation of gamma-glutamyltranspeptidase and alkaline phosphatase concentrations in blood plasma with the form of acute cholecystitis.Methods. A study of 105 patients with acute calculous cholecystitis, 35 – with chronic calculous cholecystitis (comparison group), who underwent laparoscopic cholecystectomy, was performed. At admission to the hospital, the activity of gammaglutamyltranspeptidase (GGTP) and alkaline phosphatase in blood plasma was determined by kinetic colorimetric method.Results. A direct correlation was revealed between the level of GGTP concentration and the severity of destruction in the gallbladder wall. With catarrhal cholecystitis, it was 340 ± 116.9 U/l (p < 0.05), with phlegmonous – 108.1 ± 29.5 U/l (p < 0.05), with gangrenous – 32.9 ± 7.5 U/l (p < 0.05). Along with this, a direct correlation was revealed between the concentration of alkaline phosphatase and the severity of destruction in the gallbladder wall. In catarrhal cholecystitis, the enzyme activity was 160.3 ± 34.2 U/l (p < 0.05), in phlegmonous – 129.9 ± 14.6 U/l (p < 0.05), in gangrenous – 57 ± 18.5 U/l (p < 0.05).Conclusion. Determination of the concentration of GGTP and alkaline phosphatase in combination with other diagnostic criteria makes it possible to determine the presence of destructive forms of acute cholecystitis with high specificity and sensitivity before surgery.

Biocompatible fluorescent probe for detecting mitochondrial alkaline phosphatase activity in live cells

Alkaline phosphatase (ALP) is an enzyme that actively plays a significant role in the various metabolic processes by transferring a phosphate group to the protein, nucleic acid, etc. The elevated level of ALP in blood plasma is the hallmark of inflammation/cancer. The hyperactive mitochondria in cancer cells produce an excess of ATP to fulfill the high energy demand. Thus, we have developed a fluorescent probe Mito-Phos for ALP, which can detect phosphatase expression in mitochondria in live cells. The probe Mito-Phos has shown ~15-fold fluorescence intensity increments at 450 nm in the presence of 500 ng/mL of ALP. It takes about 60 min to consume the whole amount of ALP (500 ng/mL) in physiological buffer saline. It can selectively react with ALP even in the presence of other probable cellular reactive components. It is highly biocompatible and nontoxic to the live cells. It has shown ALP expression in a dose-dependent manner by providing concomitant fluorescence images in the blue-channel region. It has localized exclusively in the mitochondria in live cells. The probe Mito-Phos is highly biocompatible with the ability to assess ALP expression in mitochondria in live cells.

Manipulation of plasma myo-inositol in broiler chickens: effect on growth performance, dietary energy, nutrient availability, and hepatic function

This study investigated the effects of graded levels of myo-inositol (INS) in diets containing 2 levels of available P on growth performance, nutrient retention, liver N, fat and vitamin E contents, INS and alkaline phosphatase (ALP) concentrations in blood plasma. A total of 120 male Ross 308 broilers were allocated to 60 small floor pens each holding 2 birds. Two basal mash diets were formulated to be nutritionally adequate for chicks at that age, with one diet designed to have the recommended available P content (RP) (4.8g/kg non-phytate P) and the other diet containing low available P (LP) (2.5g/kg non-phytate P). The 2 basal diets were split in 3 batches each and 2 of the batches were supplemented with INS at 3.0 and 30g/kg diet, with the remaining batch of each basal diet not supplemented, giving a total of 6 experimental diets. Diets were fed ad libitum to 10 pens from 7 to 21 d age following randomization. Feeding RP diets improved (P < 0.001) the birds' growth performance, mineral availability, and blood plasma ALP. Feeding RP diets reduced (P < 0.001) apparent metabolizable energy (AME), dry matter and fat availability, blood plasma INS, and hepatic vitamin E. Dietary INS did not (P > 0.05) influence bird growth, dietary AME, or nutrient retention coefficients. Feeding INS linearly increased (P < 0.05) liver weight and hepatic N content, but linearly reduced (P < 0.05) hepatic fat concentration. It also linearly increased (P < 0.001) the INS concentration in blood plasma, but did not influence (P > 0.05) the endogenous losses (measured as sialic acid concentration) in excreta. Dietary INS did not influence (P > 0.05) the hepatic vitamin E concentration but increased (P < 0.001) the ALP in the blood of birds fed 30g/kg INS. In conclusion, high-level dietary INS supplementation did not affect bird growth performance, mineral availability, and endogenous losses, and there were no interactions between INS and P.

Chemical and Biological Characteristics of Different Hydrated Monocalcium Phosphates for Broiler Chickens

Chemical and Biological Characteristics of Different Hydrated Monocalcium Phosphates for Broiler ChickensThree hydrated monocalcium phosphates differing in purity (with or without monetite, or monetite and calcite) and in crystalline structure were used in broiler chickens diets. The performance indices, concentration of Ca, P and Mg and activity of alkaline phosphatase in blood plasma, the content of these mineral elements in bones, and physico-mechanical parameters of femur and tibia bones were recorded. Body weight on 35th day of life, feed intake and mechanical parameters of bone quality were slightly affected by the type of phosphates used. Higher Ca and P concentration in blood was stated in chickens fed diets with greater purity of phosphates, but activity of alkaline phosphatase has increased with the admixture of monetite or calcite used in phosphates. The best parameters of bone quality were found in the treatment in which hydrated monocalcium phosphate (MCP) with admixture of monetite and calcite was applied. Higher concentration of both Ca and Mg in bone was determined in chickens fed diets with pure phosphates.

Cerebral monoamine metabolism in guinea-pigs with ascorbic acid deficiency.

Guinea-pigs kept on a diet deficient in vitamin C showed, after 3 weeks, a marked decrease of ascorbic acid in brain and blood leucocytes as well as of the activity of alkaline phosphatase in blood plasma. Pair-fed animals did not exhibit these changes. The alpha-methyl-p-tyrosine (alpha MpT)-induced diminution of noradrenaline in the hypothalamus and the rest of the brain was attenuated in pair-fed animals, but restored in guinea-pigs deficient in ascorbic acid. The cerebral noradrenaline content (without administration of alpha MpT) showed a decrease in both pair-fed and ascorbic acid deficient animals. The noradrenaline of the heart exhibited a similar tendency. The alpha MpT-induced dopamine decrease in the striatum of ascorbic acid deficient animals was attenuated and the dopamine content (without alpha MpT administration) decreased. Pair-fed animals showed a similar tendency. The striatal concentration of homovanillic acid (HVA) was diminished in both pair-fed and ascorbic acid deficient guinea-pigs. The cerebral content of 5-hydroxyindoleacetic acid showed a decrease in pair-fed as well as in ascorbic acid deficient animals. It is concluded that ascorbic acid deficiency enhances the turnover of brain noradrenaline, whereas under-nutrition without ascorbic acid deficiency (pair-feeding) diminishes the turnover of cerebral noradrenaline, 5-hydroxytryptamine and striatal dopamine.

Utilization of the Bone/Liver Alkaline Phosphatase Activity Ratio in Blood Plasma as an Indicator of Ascorbate Deficiency in Salmonid Fish

The goal of this study was to test the hypothesis that the ratio of liver to bone alkaline phosphatase in blood plasma reflects the ascorbate status in scurvy-prone teleost fish (rainbow trout [Oncorhynchus mykiss]). The studies focused on finding a method for distinguishing bone alkaline phosphatase present in blood plasma from other alkaline phosphatase isoforms. We tested temperature optima and thermostability of liver, kidney, gill cartilage, and intestinal alkaline phosphatases. We did not observe differences among liver, bone, and kidney enzymes with respect to temperature optima and thermostability. We partially purified alkaline phosphatase from juvenile rainbow trout vertebrae and liver using n-butanol solubilization and ammonium sulfate fractionation. We found a difference between bone alkaline phosphatase, which precipitated in 0%-20% ammonium sulfate saturation, and liver enzyme, which required 40%-50% ammonium sulfate saturation to precipitation. We conducted a series of urea inactivation studies on partially purified enzymes from liver and vertebrae. Urea differentially inhibited the enzymes with t 1/2 = 1.1 and 0.4 min, for bone and liver, respectively. Subsequently, we subjected blood plasma alkaline phosphatase to urea inhibition, and using regression analysis we calculated the ratio of liver to bone alkaline phosphatase. We found that thus obtained ratios of bone enzyme in blood plasma correlated with liver ascorbate concentration. Bone alkaline phosphatase declined in ascorbate deficiency 10-fold, whereas low ascorbate status resulted in a 3.5-fold decrease. In order to draw a general conclusion on the linearity of the response of blood plasma/bone alkaline phosphatase as an indicator of ascorbate deficiency in fish, further studies must include analysis of individual fish followed in the process of developing avitaminosis.

The Activities of GOT, Gamma-GT, Alkaline Phosphatase in Blood Plasma of Cows and Their Calves Fed from Buckets

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