Submitted: 23 March 2020 | Approved: 10 April 2020 | Published: 13 April 2020
How to cite this article: Τsompos C, Panoulis C, Triantafyllou A, Zografos CG, TsareaK, et al. The alterations effects in phosphorus of erythropoietin and U-74389G. Int J Bone Marrow Res. 2020; 3: 021-026.
Copyright License: © 2020 Τsompos C, et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Keywords: Ischemia; Erythropoietin; U-74389G; Serum phosphorus levels; Reperfusion
The alterations effects in phosphorus of erythropoietin and U-74389G
C Τsompos1*, C Panoulis2, A Triantafyllou3, CG Zografos4, K Tsarea5, M Karamperi6 and A Papalois7
1Department of Gynecology, Anticancer Hospital of Thessaloniki “Theageneio” Thessaloniki, Hellas
2Department of Obstetrics & Gynecology, Aretaieion Hospital, Athens University, Athens, Attiki, Hellas
3Department of Biologic Chemistry, Athens University, Athens, Attiki, Hellas
4Department of Surgery, Ippokrateion General Hospital, Athens University, Athens, Attiki, Hellas
5Experimental Research Centre ELPEN Pharmaceuticals, S.A. Inc., Co., Pikermi, Attiki, Hellas
6Experimental Research Centre ELPEN Pharmaceuticals, S.A. Inc., Co., Pikermi, Attiki, Hellas
7Experimental, Educational and Research Center ELPEN, European University Cyprus, School of Medicine, Hellas
*Address for Correspondence: Tsompos Constantinos, Department of Gynecology, Anticancer Hospital of Thessaloniki “Theageneio” Thessaloniki, Greece, Tel: +00302310898511; 00306946674264; Fax: 00302106811215; Email: Tsomposconstantinos@gmail.com
Aim: This study calculated the effects on serum phosphorus (P) levels, after treatment with either of 2 drugs: the erythropoietin (Epo) and the antioxidant lazaroid (L) drug U-74389G. The calculation was based on the results of 2 preliminary studies, each one of which estimated the certain influence, after the respective drug usage in an induced ischemia reperfusion (IR) animal experiment.
Materials and methods: The 2 main experimental endpoints at which the serum P levels were evaluated was the 60th reperfusion min (for the groups A, C and E) and the 120th reperfusion min (for the groups B, D and F). Specially, the groups A and B were processed without drugs, the groups C and D after Epo administration; whereas the groups E and F after the L administration.
Results: The first preliminary study of Epo presented a non significant hyperphosphoremic effect by 2.46% + 2.02% (p - value = 0.2168). However, the second preliminary study of U-74389G presented a non significant hypophosphoremic effect by 1.09% + 2.01% (p - value = 0.5771). These 2 studies were co-evaluated since they came from the same experimental setting. The outcome of the co-evaluation was that L is at least 0.4455128-fold [0.4445589 - 0.4464687] more hypophosphoremic than Epo (p - value = 0.0000).
Conclusions: The anti-oxidant capacities of U-74389G ascribe at least 0.4455128-fold [0.4445589 - 0.4464687] more effects than Epo (p - value = 0.0000).
The lazaroid U-74389G (L) may be not famous for its hypophosphoremic1 capacity (p - value = 0.5771). U-74389G as a novel antioxidant factor, implicates exactly only 262 published studies. The ischemia reperfusion (IR) type of experiments was noted in 19.08% of these studies. A tissue protective feature of U-74389G was obvious in these IR studies. The U-74389G chemically known as 21-[4-(2,6-di-1-pyrrolidinyl-4-pyrimidinyl)-1-piperazinyl]-pregna-1,4,9(11)-triene-3,20-dione maleate salt is an antioxidant complex, which prevents the lipid peroxidation either iron-dependent, or arachidonic acid-induced one. Animal kidney, liver, brain microvascular endothelial cells monolayers and heart models were protected by U-74389G after IR injury. U-74389G also attenuates the leukocytes; down-regulates the pro-inflammatory gene; treats the endotoxin shock; produces cytokine; enhances the mononuclear immunity; protects the endothelium and presents anti shock property.
Erythropoietin (Epo) even if is not famous for its hyperphosphoremic2 action (p - value = 0.2168), it can be used as a reference drug for comparison with U-74389G. Although Epo is met in over 31,502 published biomedical studies, only a 3.7% of them negotiate the known type of IR experiments. Nevertheless, Epo as a cytokine, it is worth of being studied about its effects on serum phosphorus (p) levels too. This experimental work tried to compare the effects of the above drugs on a rat induced IR protocol. They were tested by calculating the serum p levels alterations. Phosphorus is essential for life. Phosphates (compounds containing the phosphate ion, PO43−) are a component of DNA, RNA, ATP, and phospholipids. Elemental phosphorus was first isolated from human urine and bone ash was an important early phosphate source. Bone marrow is composed of hematopoietic cells, marrow adipose tissue, and supportive stromal cells. Human marrow produces approximately 500 billion blood cells per day, which join the systemic circulation. All types of hematopoietic cells, including both myeloid and lymphoid lineages, are created in bone marrow. Hematopoietic cells are very rich in DNA, RNA, ATP, and phospholipids. Since erythropoietin stimulates red blood cell production (erythropoiesis) in the bone marrow; an assumption was set that the alterations Epo causes on phosphorus levels, may reflect related alterations on erythropoiesis. It is claimed that epo may have antioxidant properties; thus, this assumption for epo is compared with a similar one with the antioxidant drug L.
The Vet licenses under 3693/12-11- 2010 & 14/10-1-2012 numbers, the granting company and the experiment location are mentioned in preliminary references [1,2]. The human animal care of Albino female Wistar rats, the 7 days pre-experimental ad libitum diet, the non-stop intra-experimental anesthesiologic techniques, the acidometry, the electrocardiogram, the oxygen supply and post-experimental euthanasia are also described in preliminary references. Rats were 16 – 18 weeks old. They were randomly assigned to six (6) groups consisted in N = 10. The stage of 45 min hypoxia was common for all 6 groups. Afterwards, reperfusion of 60 min was followed in group A; reperfusion of 120 min in group B; immediate Epo intravenous (IV) administration and reperfusion of 60 min in group C; immediate Epo IV administration and reperfusion of 120 min in group D; immediate U-74389G IV administration and reperfusion of 60 min in group E; and immediate U-74389G IV administration and reperfusion of 120 min in group F. The dose height assessment for both drugs are described at preliminary studies as 10 mg/Kg body mass.
Ischemia was caused by laparotomic clamping the inferior aorta over renal arteries with forceps for 45 min. The clamp removal was restoring the inferior aorta patency and reperfusion. After exclusion of the blood flow, the protocol of IR was applied, as described above for each experimental group. The drugs were administered at the time of reperfusion; through inferior vena cava catheter. The p levels were determined at 60th min of reperfusion (for A, C and E groups) and at 120th min of reperfusion (for B, D and F groups). Along, non relation was rised between p values with animals’ mass (p - value = 0.5911).
Table 1 presents the (%) hyperphosphoremic influence of Epo regarding reoxygenation time. Also, Table 2 presents the (%) hypophosphoremic influence of U-74389G regarding reperfusion time. Chi-square tests were applied using the ratios which produced the (%) results per endpoint. The outcomes of chi-square tests are depicted at table 3.
The successive application of chi-square tests revealed that U-74389G caused hypophosphoremia at least by 0.86185944-fold [0.71786427 - 1.0347395] than Epo at 1h (p - value = 0.1111), at least by 0.4096059-fold [0.4088905 - 0.4103226] than Epo at 1.5h (p - value = 0.0000), at least by 0.1675922-fold [0.1672522 - 0.167933] than Epo at 2h (p - value = 0.0000), by 5.120084-fold [5.102681 - 5.137547] less than Epo (p - value = 0.0000) without drugs and at least by 0.4455128-fold [0.4445589 - 0.4464687] than Epo whether all variables have been considered (p - value=0.0000).
The unique available study investigating the hypophosphoremic effect of U-74389G was the preliminary one1. Although the most famous activities of neuroprotection and membrane-stabilization properties, it accumulates in the cell membrane, protecting vascular endothelium from peroxidative damage but hardly penetrates the blood-brain barrier. It elicits a beneficial effect in ototoxicity and Duchenne muscular dystrophy. It increases γgt, superoxide dismutase (SOD) and glutathione (GSH) levels in oxygen-exposed cells. It treats septic states and acts as immunosuppressant in flap survival. It prevents the learning impairments, it delays the early synaptic transmission decay during hypoxia improving energetic state of neurons. It shows antiproliferative properties on brain cancer cells and is considered as a new promising anti inflammatory drug for the treatment of reperfusion syndrome in IR injuries.
The same authors confirmed  the short-term hyperphosphoremic effect of Epo preparations in non iron deficient individuals. Ozelsancak, et al.  reported that hemodialysis (HD) patients with CSVD had lower sCr (p < 0.0001) and phosphorus (p < 0.007) levels than normal subjects. Takahashi, et al. demonstrated  an increase in the magnetization transfer ratio asymmetry (MTRasym), which reflects Cr concentration of ischemic hindlimbs, along with a decrease of PCr; whereas they developed phosphorus magnetic resonance spectroscopy (31 P MRS) obtained at 11.7T calculated in severe ischemic, mild ischemic and control hindlimbs of mouse skeletal muscle in C57BL/6 mice. Dubský, et al. showed  a significant increase of transcutaneous oxygen pressure (TcPO2) among the rest (phosphocreatine, adenosine triphosphate and inorganic phosphate) and dynamic (mitochondrial capacity and phosphocreatine recovery time) 31P-MRS parameters at baseline and 3 months after autologous cell therapy on the dorsum of the foot. Stephens, et al. demonstrated  that a single high dose of phosphate (2,000 mg) did not augment blood pressure in response to exercise or isolated muscle metaboreflex activation in young healthy men. Wang Y, et al. claim that penehyclidine hydrochloride (PHC) can effectively antagonize  the symptoms of central and peripheral poisoning caused by organophosphorus poisoning. Gruson, et al. claimed  that the increase of fibroblast growth factor 23 (FGF-23), a key hormone for the regulation of the phosphorus homeostasis, participates to cardiac hypertrophy and remodeling in heart failure. Hart, et al. repeated  the free-flow control conditions (FF) and reactive hyperemia (RH) trials under hyperoxic conditions (FF+ 100% O2 and RH + 100% O2) in skeletal gastrocnemius muscle of patients with peripheral artery disease. Anselmo, et al. attenuated  IR-induced renal changes, with reduction of plasmatic phosphorus as well as reducing kidney expression of iNOS, nitrotyrosine and macrophage influx after pre-treatment with 75 mg of Brazil nuts. Tarui, et al. evaluated  the outcome and risk factors related  with increased creatinine phosphorus kinase in patients undergoing minimally invasive cardiac operation in mitral valve problem. Dattilo, et al. associated  hypovitaminosis D beyond calcium and phosphorus with the genesis of rheumatic, autoimmune, neoplastic and cardiovascular diseases in patients particularly with heart failure. Hirose, et al. found  greater LV mass index or serum calcium-phosphorus product in dialysis patients with positive myocardial ischemia despite an FFR > 0.76. Abdurrachim, et al. investigated  cardiac energetics non-invasively in vivo by 31P magnetic resonance spectroscopy (MRS), by detecting 31P-containing metabolites involved in energy supply and buffering and understanding of cardiac energy metabolism in heart failure and diabetes. El Sharkawy, et al. observed  statistically significant higher levels of serum miRNA 499 in all the studied patients with cardiovascular diseases and complications than the levels of miRNA 499 in healthy controls (p < 0.0001). High-flux membrane seems to be less efficient in miRNA 499 clearance in cardiac patients on hemodialysis. Andrulli S, et al. significantly related  an increased risk of lower limb ulcers with blood levels of phosphorus among other variables in dialysis patients. Yuan, et al. analyzed  the effects of surgical total removal of parathyroid gland (PTG) tissue in rats. Chatel, et al. used  magnetic resonance spectroscopy of phosphorus 31, phosphocreatine and inorganic phosphate concentrations throughout two standardized protocols of a spontaneous muscular vaso-occlusive crisis in rest - exercise - recovery at two different intensities in sickle cell disease (SCD) mice. Němcová A, et al. found enabled  phosphorus magnetic resonance spectroscopy (31P MRS) to evaluate oxidative muscle impaired metabolism in patients with complicated diabetes. Thus, significantly higher Pi and pH (both p < 0.01) were noticed in patients with CLI than healthy control ones. Ezzati et al. assessed  the whole-brain (phosphorus-31 and regional proton MRS biomarkers) nucleotide triphosphate/exchangeable phosphate pool was similar (p = 0.73) over 48h in large White male piglets. Kamath, et al. recommend  to all patients with a history of previous thyroid operation, who come with vague symptoms like fatigue, muscle aches to undergo estimation of serum calcium, phosphorus and parathyroid hormone (PTH) screened for delayed hypoparathyroidism. Carlbom et al. consider  phosphomonoesters(PME)/Pi ratio as the most discriminatory variable at prolonged CIT. 31P-MRS may provide quantitative parameters for evaluating graft viability (ex vivo and is a promising tool for objective non-invasive assessment of the quality of human pancreas grafts prior to transplantation or islet isolation. Lowe, et al. positively correlated  anti-inflammatory cytokine IL-17E with serum 25(OH) vitamin D insufficiency present in the majority of term HIE neonates. Layec, et al. assessed muscle metabolism and peripheral hemodynamics in healthy, untrained, elderly individuals subjected  to dynamic plantar flexion exercise and other imaging examinations including phosphorus magnetic resonance spectroscopy (31P-MRS). Groenendaal, et al. were  led to the concept of secondary energy failure after phosphorus magnetic resonance spectroscopy (MRS) in infants with HIE. Li, et al. found the ratio of pSer16-PLB/PLB expression to decrease calcium overload obviously decreased  (p < 0.05); whereas the sarcoplasmic reticulum calcium transport ATPase SERCA 2a expression risen in the gastrodin group in a dose-dependent manner (p < 0.05) along with MIRI and inflammation injury alleviation. Liu, et al. acquired  31P magnetic resonance spectroscopy (31P-MRS) to quantify changes in phosphate metabolites and muscle oxygenation in Goto-Kakizaki (GK) non-obese type 2 diabetes (T2D) rats and Wistar (control) rats. Inci, et al. did not associated the soluble Klotho (s-Klotho) levels  with phosphorus and PTH levels in diabetic nephropathy patients. Brown, et al. related  the progression of established chronic kidney disease CKD with dietary phosphorus intake, in cats. Broad, et al. acquired  successive whole-brain phosphorus-31 and regional proton MRS after hypoxia-ischemia in newborn male Large White piglets. Ezzati, et al. assessed  increased whole brain phosphorus-31 MRS ATP (p = 0.039) and immediate remote ischemic postconditioning (RIPostC) as a brain protective therapy for babies with NE with protection in white matter over the 48h after HI in large White female newborn piglets. Wilder, et al. confirmed  by intracellular 31-phosphorus (31P) nuclear magnetic resonance (NMR) spectroscopy that insertion of an intraventricular balloon IVB inflation has profound antiarrhythmic effects, likely due to inflation-induced localized ischaemia in rat Langendorff heart preparation.
The quoted references show the important diagnostic value of p through the metabolic level, as the buffering role of reoxygenation and cytokines on p levels. According to above, table 3 shows that U-74389G has at least 0.4455128-fold [0.4445589 - 0.4464687] more hypophosphoremic than Epo whether all variables have been considered (p - value = 0.0000); a trend accentuated along time, in Epo non-deficient rats. A meta-analysis of these ratios from the same experiment, for 30 other seric variables, provides comparable results (Table 4) .
The anti-oxidant agent U-74389G was proved having at least 0.4455128-fold [0.4445589 - 0.4464687] more hypophosphoremic than Epo whether all variables have been considered (p - value = 0.0000); a trend attenuated along the short term time frame of the experiment in rats. A biochemical investigation remains about how U-74389G mediates in these actions.
Acknowledged in preliminary studies
“All applicable international, national, and/or institutional guidelines for the care and use of animals were followed.”
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