| Name | alkaline phosphatase |
|---|---|
| Synonyms | ALP 1; Alkaline phosphatase; ALPG; ALPPL; ALPPL 2; ALPPL2; GCAP; Germ cell alkaline phosphatase… |
| Name | oxytetracycline |
|---|---|
| CAS |
| PubMed | Abstract | RScore(About this table) | |
|---|---|---|---|
| 16635103 | Pari L, Gnanasoundari M: Influence of on oxytetracycline mediated oxidative damage in rat liver. Basic Clin Pharmacol Toxicol. 2006 May;98(5):456-61. Intraperitonial administration of oxytetracycline 200 mg/kg for 15 days resulted a significant elevation in serum hepatospecific markers such as transaminase, transaminase, alkaline phosphatase, lactate dehydrogenase, and and the levels of lipid peroxidation markers (thiobarbituric acid reactive substances (TBARS) and lipid hydroperoxides) in liver. |
12(0,0,2,2) | Details |
| 19862962 | Yang Q, Zhang J, Zhu K, Zhang H: Influence of oxytetracycline on the structure and activity of microbial community in wheat rhizosphere soil. J Environ Sci. 2009;21(7):954-9. Among the four soil enzymes (alkaline phosphatase, acidic phosphatase, dehydrogenase and urease), only alkaline phosphatase was sensitive to oxytetracycline exposure with 41.3% decline of the enzyme activity at 10 mg/kg antibiotic and further decrease of 64.3%-80.8% when the dosage over 30 mg/kg. |
6(0,0,1,1) | Details |
| 9567764 | Saraswat B, Visen PK, Patnaik GK, Dhawan BN: Protective effect of picroliv, active constituent of Picrorhiza kurrooa, against oxytetracycline induced hepatic damage. Indian J Exp Biol. 1997 Dec;35(12):1302-5. Picroliv also antagonised alterations in enzyme levels (GOT, GPT, and alkaline phosphatase) in isolated hepatocytes and serum, induced by oxytetracycline (200 mg/kg, i.p.) feeding. |
6(0,0,1,1) | Details |
| 3371716 | Batt RM, McLean L, Riley JE: Response of the jejunal mucosa of dogs with aerobic and anaerobic bacterial overgrowth to antibiotic therapy. Gut. 1988 Apr;29(4):473-82. Aerobic overgrowth was initially associated with a marked loss of the main brush border component of alkaline phosphatase activity; this recovered following treatment, suggesting that aerobic bacteria may cause reversible damage to the hydrophobic region of the brush border membrane. |
1(0,0,0,1) | Details |
| 7871380 | Vetvik K, Schrumpf E, Mowinckel P, Aase S, Andersen KJ: Effects of and eradication of Helicobacter pylori on gastric and duodenal mucosal enzyme activities and DNA in duodenal ulcer patients. Scand J Gastroenterol. 1994 Nov;29(11):995-1000. The activities of the brush-border enzymes lactase, neutral-alpha-glucosidase, alkaline phosphatase, leucyl-beta-naphthylamidase, and gamma-glutamyltransferase (gamma-GT) increased significantly in the duodenal bulb and the descending duodenum during treatment with In study II 22 duodenal ulcer patients were given bismuth subnitrate, oxytetracycline, and metronidazole (triple therapy) for 2 weeks to eradicate H. pylori. |
1(0,0,0,1) | Details |
| 10755443 | Sovak G, Weiss A, Gotman I: Osseointegration of Ti6Al4V alloy implants coated with titanium nitride by a new method. J Bone Joint Surg Br. 2000 Mar;82(2):290-6. Mineralisation around the implants was also confirmed by labelling with oxytetracycline. Strong activity of alkaline phosphatase and weak activity of tartrate-resistant acid phosphatase were shown histochemically. |
1(0,0,0,1) | Details |
| 12934022 | Chambler AF, Pitsillides AA, Emery RJ: Acromial spur formation in patients with rotator cuff tears. J Shoulder Elbow Surg. 2003 Jul-Aug;12(4):314-21. The sites of oxytetracycline labeling appear to correlate with the sites of high ALP and G6PD activity, which supports the concept of spur formation being a secondary phenomenon in the presence of established rotator cuff tears. Mineral apposition analysis and quantitative cytochemical techniques for glucose-6-phosphate dehydrogenase (G6PD) activity (pentose phosphate pathway), alkaline phosphatase (ALP) activity (osteoblast activity), and tartrate-resistant acid phosphatase (TRAP) activity (osteoclast phenotype) were used to examine the distribution and level of activity of selected marker enzymes within the acromial spur insertion into the coracoacromial ligament in order to establish whether local behavior of bone cells is consistent with the proposed secondary development of the acromial spur. |
1(0,0,0,1) | Details |