Effect of cryopreserved placenta extract on some biochemical indices of therapeutic efficiency and toxicity of diclofenac sodium in adjuvant-induced experimental arthritis

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Abstract

Relevance. Non-steroidal anti-inflammatory drugs are among the top requested ones in the clinic of internal medicine. However, these drugs are associated with a wide range of adverse reactions involving a number of organs and systems, in particular the gastrointestinal tract, cardiovascular system and kidneys.

The aim of the study is to characterize the effect of the combined use of cryopreserved placenta extract and diclofenac sodium on the prooxidant-oxidative system, the activity of inflammatory, destructive and cytolytic processes, as well as protein and lipid metabolism in rats with experimental rheumatoid arthritis.

Results. The administration of diclofenac sodium and cryopreserved placenta extract to rats with adjuvant arthritis normalized the level of active products of thiobarbituric acid and hence was indicative of the neutralization of an arthritis-induced oxidative stress. A statistically significant (p=0.01) increase of in a superoxide dismutase activity (by 30.6% relative as compared with rats of the control group) has also been established. An increase in the anti-inflammatory properties of diclofenac sodium in the combined use of diclofenac sodium with a cryopreserved placenta extract has been found out. The level of C-reactive protein decreased (p<0.001) by 61.1% as compared with the untreated rats, and the level of seromucoid has been significantly (p<0.01) decreased by 17.1% as compared with the rats of the monotherapy group treated with the studied NSAIDs. It was shown that alanine aminotransferase and aspartate levels were significantly lower (by 38.9%, p<0.01 and by 37.9%, p<0.01, respectively) as compared with those of the animals that had been administrated with diclofenac sodium. Their indices were by 16.7% (p=0.02) and 17.2% (p<0.001) lower than the indices of the control group rats with untreated adjuvant arthritis. The established changes of aminotransferases levels indicate the ability of a cryopreserved placenta extract to level not only an arthritis-induced cytolytic syndrome, but also a diclofenac-induced one. The combined use of cryopreserved placenta extract and diclofenac sodium was accompanied by the normalization of the total lipids level and phospholipids in the blood serum of rats against the background of experimental rheumatoid arthritis. Thus, the content of phospholipids in the lipid pool statistically significantly (p=0.02) increased by 22.6% as compared with the indices of the animals with adjuvant arthritis without treatment.

Conclusion. The study showed that the combined use of diclofenac sodium and cryopreserved placenta extract leads to the restoration of the balance of the prooxidant-antioxidant system that is more pronounced than monotherapy with diclofenac sodium. A decrease in the activity of inflammatory, destructive and cytolytic processes, as well as the restoration of lipid metabolism in the rats with experimental rheumatoid arthritis, has also been observed

About the authors

Fedir V. Hladkykh

Institute for Problems of Cryobiology and Cryomedicine of the National Academy of Sciences of Ukraine;State Organization “Grigoriev Institute for Medical Radiology and Oncology of the National Academy of Medical Sciences of Ukraine”

Author for correspondence.
Email: fedir.hladkykh@gmail.com
ORCID iD: 0000-0001-7924-4048

postgraduate student (Doctor of Philosophy in Health Care in specialty «222 – Medicine») of the Department of Experimental Cryomedicine; Junior Research fellow of the Groups of Radiation Pathology and Palliative Medicine at the Radiology Department

Ukraine, 23, Pereyaslavska Str., Kharkiv, Ukraine, 61015; 82, Pushkinska Str., Kharkiv, Ukraine, 61024

Mykola O. Chyzh

Institute for Problems of Cryobiology and Cryomedicine of the National Academy of Sciences of Ukraine

Email: chizh.cryo@gmail.com
ORCID iD: 0000-0003-0085-296X

Candidate of Sciences (Medicine), Senior Researcher, Acting Head of the Department of Experimental Cryomedicine

Ukraine, 23, Pereyaslavska Str., Kharkiv, Ukraine, 61015

Anna O. Manchenko

Institute for Problems of Cryobiology and Cryomedicine of the National Academy of Sciences of Ukraine

Email: anna.gorlenko@gmail.com
ORCID iD: 0000-0001-5982-4504

Candidate of Sciences (Medicine), Junior Research fellow of the Department of Experimental Cryomedicine

Ukraine, 23, Pereyaslavska Str., Kharkiv, Ukraine, 61015

Iryna V. Belochkina

Institute for Problems of Cryobiology and Cryomedicine of the National Academy of Sciences of Ukraine

Email: ibelochkina@ukr.net
ORCID iD: 0000-0003-0090-2971

Candidate of Sciences (Biology), Senior Researcher of the Department of Experimental Cryomedicine

Ukraine, 23, Pereyaslavska Str., Kharkiv, Ukraine, 61015

Iryna P. Mikhailova

Institute for Problems of Cryobiology and Cryomedicine of the National Academy of Sciences of Ukraine

Email: expcryomed@gmail.com
ORCID iD: 0000-0001-9388-2820

Researcher of the Department of Experimental Cryomedicine

Ukraine, 23, Pereyaslavska Str., Kharkiv, Ukraine, 61015

References

  1. Zeng C, Wei J, Persson MSM, Sarmanova A, Doherty M, Xie D, Wang Y, Li X, Li J, Long H, Lei G, Zhang W. Relative efficacy and safety of topical non-steroidal anti-inflammatory drugs for osteoarthritis: a systematic review and network meta-analysis of randomised controlled trials and observational studies. British Journal of Sports Medicine. 2018;52(10):642–50. DOI: https://doi.org/10.1136/bjsports-2017-098043.
  2. Balabantseva AP, Karateev AE. Frequency and clinical and endoscopic features of combined NSAID-induced gastrointestinal injuries. Modern rheumatology. 2018;12(4):95–100. DOI: https://doi.org/10.14412/1996-7012-2018-4-95-100. Russian
  3. Ushkalova EA, Zyryanov SK, Zatolochina KE. Safety and tolerance of NSAIDs: focus on aceclofenac. Medical Council. 2019;9:110–20. DOI: https://doi.org/10.21518/2079-701X-2019-9-110-120. Russian
  4. Fischbach W. Drug-induced gastrointestinal bleeding. Internist. 2019;60(6):597-607. DOI: https://doi.org/10.1007/s00108-019-0610-y.
  5. Trinus FP. Evolutionary evidence about the mechanism of non-steroidal anti-pyretic drugs and analgesics-antipyretics. Pharmacology and toxicology. 2012;2(27):68–72. Ukrainian
  6. Hladkykh F. Multimodal analgesia: polypharmacy in anesthesia or rational use of non-steroidal anti-inflammatory drugs to prevent chronic pain. Traktoriya nauki: international electronic journal of science = Traektoriâ Nauki = Path of Science. 2020;6(7):4009–18. DOI: http://dx.doi.org/10.22178/pos.60-5. Russian
  7. Bally M, Dendukuri N, Rich B, Nadeau L, Helin-Salmivaara A, Garbe E, Brophy JM. Risk of acute myocardial infarction with NSAIDs in real world use: bayesian meta-analysis of individual patient data. BMJ. 2017 May 9;357:j1909. doi: 10.1136/bmj.j1909.
  8. Karateev AE, Nasonov EL, Ivashkin VT, Martynov AI, Yakhno NN, Arutyunov GP, Alekseeva LI, Abuzarova GR, Evseev MA, Kukushkin ML, Kopenkin SS, Lila AM, Lapina TL, Novikova DS, Popkova TV, Rebrov AP, Skorobogatykh KV, Chichasova NV. Rational use of non-steroidal anti-inflammatory drugs. Clinical guidelines. Scientific and practical rheumatology. 2018; 56:1–29. DOI: https://doi.org/10.14412/1995-4484-2018-1-29. Russian
  9. Cooper C, Chapurlat R, Al-Daghri N, Herrero-Beaumont G, Bruyere O, Rannou F, Roth R, Uebelhart D, Reginster JY. Safety of oral non-selective non-steroidal anti-Inflammatory drugs in osteoarthritis: what does the literature say? Drugs & Aging. 2019;36(1):15–24. DOI: https://doi.org/10.1007/s40266-019-00660-1.
  10. Lazebnik LB, Golovanova EV, Alekseenko SA, Bakulina NV, Baranovskiy AYu, Belova GV, Bordin DS, Vyuchnova ES, Gaidukova IZ, Gimaeva ZF, Kashkina EI, Kozlova IV, Kokorin VA, Lapina ED, Li ED, Miguskina EI, Mironchev OV, Onuchina EV, Okhlobystin AV, Pasechnikov VD, Pakhomova IG, Pozdnyakova OYu, Putintseva IV, Sarsenbaeva AS, Sviridova TN, Simanenkov VI, Simonova ZhG, Sitkin SI, Tkachenko EI, Turkina SV, Khabarova YuA, Shevyakov MA, Yakovenko EP, Yakovlev AA, Yankovaya TN. Recommendations for the prevention and treatment of esophago-gastro-enterocolopathies induced by nonsteroidal anti-inflammatory drugs. Experimental and Clinical Gastroenterology. 2018;3(151):4–18. Access: https://www.nogr.org/jour/article/view/567/562. Russian
  11. Yang JH, Lee BH, Eum KS, Suk KS, Park JO, Kim HS, Lee HM, Moon SH. Prevalence of gastrointestinal and cardiovascular risk in patients with degenerative lumbar spinal disease. Clinics in Orthopedic Surgery. 2020;12(3):343–52. DOI: https://doi.org/10.4055/cios20021.
  12. Karateev AE. Do non-steroidal anti-inflammatory drugs have a pathogenetic effect? Modern rheumatology. 2012;4:13–22. Russian
  13. Karateev AE. Selective inhibitors of cyclooxygenase-2 and “protected” non-steroidal anti-inflammatory drugs: two methods of preventing drug complications. Clinical Medicine. 2014;8:54–61. Russian
  14. Davis A, Robson J. The dangers of NSAIDs: look both ways. British Journal of General Practice. 2016;66(645):172–173. DOI: https://doi.org/10.3399/bjgp16X684433.
  15. Dovgan EV. Clinical pharmacology of non-steroidal anti-inflammatory drugs: a course towards safety. Russian medical journal. 2017;13: 979–85. Russian
  16. Stepanyuk NH, Hladkykh FV, Basarab OV. Analysis of Adverse Reaction of Analgesics, Antipyretics and Non-Steroidal Anti-Inflammatory Drugs Prescribed by Physicians of Health Care Facilities in Podilskyi Region during 2015. Galician Medical Journal. 2016;2(23):60–3. Available from: http://ojs.ifnmu.edu.ua/index.php/gmj/article/view/545.
  17. Bjarnason I, Takeuchi K. Intestinal permeability in the pathogenesis of NSAID-induced enteropathy. J Gastroenterol. 2009;44 Suppl 19:23-9. doi: 10.1007/s00535-008-2266-6.
  18. Golovanova EV. Protection of the mucous membrane of the gastrointestinal tract from the damaging effect of non-steroidal anti-inflammatory drugs. Clinical gerontology. 2017;1–2:47–51. Russian
  19. Hladkykh FV. Preventive and therapeutic strategies for the pharmaco-correction of gastropathy induced by nonsteroidal anti-inflammatory drugs. Reviews on clinical pharmacology and drug therapy. 2017;4:14–23. DOI: http://dx.doi.org/10.17816/RCF15414-23. Russian
  20. Kuksgauz IA, Shekunova EV, Kashkin VA, Faustova NM, Gushchin YaA, Makarova MN, Makarov VG. Study of the gastroprotective effect of the drug Alflutop on the model diclofenac-induced gastropathy in rats. Experimental and Clinical Gastroenterology. 2019;5:15–21. DOI: https://doi.org/10.31146/1682-8658-ecg-165-5-15-21. Russian
  21. Gulevsky AK, Abakumova EU, Moiseeva NN, Dolgikh OL. Influence of umbilical cord blood fraction (up to 5 kDa) of cattle on biochemical parameters of blood in experimental subchronic gastric ulcer in rats. Ukrainian Biochemical Journal. 2008;80(2):120–7. Russian
  22. Zharikov AYu, Lorenz SE, Bobrov IP, Mazko ON, Makarova OG Search for new oligopeptide molecules for pharmacological correction of NSAID-induced gastric ulcer. Biomedicine. 2019;15(3):90–7. DOI: https://doi.org/10.33647/2074-5982-15-3-90-97. Russian
  23. Gulida MO, Miroshnichenko EB, Birch HІ, Garyachiy EB. Application of placenta extract in the complex treatment of patients with rheumatoid arthritis. Experimental and clinical medicine. 2014;1(62):168–71. Russian
  24. Kapustianska AA. Stagnation of the drug “Cryocell-cryoextract of the placenta” in the complex treatment of gouty arthritis with metabolic arthritis. Actual problems of contemporary medicine: Bulletin of the UMSA. 2010;10(30):54–8. Ukrainian
  25. Pogozhykh O, Prokopyuk V, Figueiredo C, Pogozhykh D. Placenta and placental derivatives in regenerative therapies: experimental studies, history, and prospects. Stem Cells International. 2018;2018:1–14. DOI: https://doi.org/10.1155/2018/4837930.
  26. Shepitko KV. Application of cryopreserved placenta preparations in the small intestine pathologies in rats for their further use in exigent conditions. Bulletin of problems biology and medicine. 2019;4(154):56–61. DOI: http://doi.org/10.29254/2077-4214-2019-4-2-154-56-61.
  27. Petrenko YA, Petrenko AY, Martin I, Wendt D. Perfusion bioreactor-based cryopreservation of 3D human mesenchymal stromal cell tissue grafts. Cryobiology. 2017;76:150–3. DOI: http://doi.org/10.1016/j.cryobiol.2017.04.001.
  28. Rogulska O, Tykhvynska O, Revenko O, Grischuk V, Mazur S, Volkova N, Vasyliev R, Petrenko A, Petrenko Y. Novel Cryopreservation Approach Providing Off-the-Shelf Availability of Human Multipotent Mesenchymal Stromal Cells for Clinical Applications. Stem Cells International. 2019;2019:4150690. DOI: https://doi.org/10.1155/2019/4150690.
  29. Pogozhykh D, Pogozhykh O, Prokopyuk V, Kuleshova L, Goltsev A, Blasczyk R, Mueller T. Influence of temperature fluctuations during cryopreservation on vital parameters, differentiation potential, and transgene expression of placental multipotent stromal cells. Stem Cell Research & Therapy. 2017;8(1):66. DOI: https://doi.org/10.1186/s13287-017-0512-7.
  30. Kapustyanska AA The use of the drug “Cryocell-cryoextract of the placenta” in the complex treatment of exacerbation of gouty arthritis with metabolic arthritis. Actual problems of modern medicine: Bulletin of the Ukrainian Medical and Dental Academy. 2010.10.(30);54–8. Russian
  31. Prokopyuk V. Yu., Falko OV, Musatova IB, Prokopyuk OS, Roenko OO, Terekhova OO, Chub OV. Critical preservation and low-temperature cure of placental biosynthesis. Problems of Criobiology and Criomedicine. 2015;25(4):291–310. Ukrainian
  32. Hladkykh FV, Chyzh NA. Protection mechanisms of the gastric mucosa under conditions of placental cryoextract use in diclofenac-induced gastropathy. Collection of materials of the satellite remote scientific-practical conference of students and young scientists “Fundamental Science in Modern Medicine – 2021”. Minsk: Foundation of education “Bilorussian State Medical University”. 2021:436–40. Russian
  33. Hladkykh FV, Chyzh NA, Sleta IV. Study of gastroprotective activity of cryopreserved placenta extract in ibuprofen-induced gastric lesion in experiment. Materials of the VII Republican Scientific-Pak conference of young scientists “Modern achievements of young scientists in medicine - 2020”. Grodno. Grodno: Foundation of education “Grodno State Medical University”. 2020:57–60. Russian
  34. Hladkykh FV, Chyzh MO. Modulation of meloxicam-induced changes in gastrointestinal and motor activity of the stomach by applying placenta cryoextract. Proceedings of the Shevchenko Scientific Society. Medical Sciences. 2021;64(1):84–94. DOI: https://doi.org/10.25040/ntsh2021.01.08 Access: https://mspsss.org.ua/index.php/journal/article/view/400. Ukrainian
  35. Gryshchenko NG, Klimenko NA, Gorgol NI, Tatarko SV. Effect of placental cryoextract on chronic inflammation of the ovaries in mice. Medicine today and tomorrow. 2010;2–3(47–8):7–17. Available from: http://dspace.nbuv.gov.ua/handle/123456789/44519
  36. Brun LV, Makolinets VI. Investigation of the effect of low-intensity infrared laser radiation on the concentration of diclofenac sodium in the blood plasma of rats by high-performance liquid chromatography. Medical and clinical chemistry. 2016;18(2):54–9. Ukrainian. Available from: http://nbuv.gov.ua/UJRN/Medkh_2016_18_2_12
  37. Rybolovlev YuR, Rybolovlev RS Dosing of substances for mammals according to the constants of biological activity. Reports of the USSR Academy of Sciences. 1979;247(6):1513–6. Russian
  38. Orlovskaya IA, Tsyrendorzhiev DD, Shchelkunov SN Rheumatoid arthritis: laboratory models of the disease. Medical immunology. 2015;17(3):203–10. Russian
  39. Gromyko MV, Gritsuk AI. Experimental models of rheumatoid arthritis. Problems of health and ecology. 2012;2(32):115–8. Russian
  40. Freund J. Some aspects of active immunization. Annual Review of Microbiology. 1947;1:291–308.
  41. Choudhary N, Bhatt LK, Prabhavalkar KS. Experimental animal models for rheumatoid arthritis. Immunopharmacology and Immunotoxicology. 2018;40(3):193–200. DOI: https://doi.org/10.1080/08923973.2018.1434793.
  42. Alavala S, Nalban N, Sangaraju R, Kuncha M, Jerald MK, Kilari EK, Sistla R. Anti-inflammatory effect of stevioside abates Freund’s complete adjuvant (FCA)-induced adjuvant arthritis in rats. Inflammopharmacology. 2020;28(6):1579–97. DOI: https://doi.org/10.1007/s10787-020-00736-0.
  43. Asakawa T, Matsushita S. Сoloring condition of thiobarbituric acid test for detecting lipid hydroperoxides. Lipids. 1980;15(3):137–40.
  44. Kostyuk VA, Potapovich AI, Kovaleva ZhV. A simple and sensitive method for determining the activity of suprokid dismutase, based on the oxidation reaction of quercetin. Questions of medicinal chemistry. 1990;2:88–91. Russian
  45. Bligh EG, Dyer WI. A rapid method of total lipid extraction and purification. Canadian Journal of Biochemistry and Physiology. 1959;37(8):911–7.
  46. Svetashev VI, Vaskovsky VE. A simplified technique for thin layer microchromatography of lipids. Journal of Chromatography. 1972;67:376–8.
  47. Vaskovsky VE, Kostetsky EY, Vasendin IM. A universal reagent for phospholipid analysis. Journal of Chromatography. 1975;114:129–41.
  48. Mititelu RR, Padureanu R, Bacanoiu M, Padureanu V, Docea AO, Calina D, Barbulescu AL, Buga AM. Inflammatory and oxidative stress markers-mirror tools in rheumatoid arthritis. Biomedicines. 2020;8(5):125. DOI: https://doi.org/10.3390/biomedicines8050125.
  49. Voitenko NG, Makarova MN, Zueva AA Variability of blood biochemical parameters and the establishment of reference intervals in preclinical studies. Communication 1: rats. Laboratory animals for scientific research. 2020;1:47–53. DOI: https://doi.org/10.29296/2618723X-2020-01-06. Russian
  50. Hladkykh FV, Stepanyuk NH. Characteristics of the therapeutic effect of ibuprofen and the combination of hematological indicators on the model of adjuvant arthritis in rats. Lviv Medical Journal. 2015;4:64–70. Ukrainian. Available from: http://nbuv.gov.ua/UJRN/Lmch_2015_21_4_14
  51. Podolskiy VV, Podolskiy VV. Peroxidation of lipids as a manifestation of oxidative stress in the organisms of women because of reproductive health symptoms on aphids of somatoform diseases due to disorders of vegetative homeostasis. Obstetrics and obstetrics. 2017;2:98–104. DOI: https://doi.org/10.11603/24116-4944.2017.2.8095. Ukrainian
  52. Agrahari G, Sah SK, Nguyen CT, Choi SS, Kim HY, Kim TY. Superoxide dismutase 3 inhibits LL-37/KLK-5-mediated skin inflammation through modulation of EGFR and associated inflammatory cascades. Journal of Investigative Dermatology. 2020;140(3):656–65. DOI: https://doi.org/10.1016/j.jid.2019.08.434.
  53. Nguyen NH, Tran GB, Nguyen CT. Anti-oxidative effects of superoxide dismutase 3 on inflammatory diseases. Journal of Molecular Medicine. 2020;98(1):59–69. DOI: https://doi.org/10.1007/s00109-019-01845-2.
  54. Suchdev PS, Williams AM, Mei Z, Flores-Ayala R, Pasricha SR, Rogers LM, Namaste SM. Assessment of iron status in settings of inflammation: challenges and potential approaches. The American Journal of Clinical Nutrition. 2017;106(6):1626–33. DOI: https://doi.org/10.3945/ajcn.117.155937.
  55. Iwanczak B, Ruczka M, Matusiewicz M, Pytrus T, Matusiewicz K, Krzesiek E. Correlation between biomarkers (calprotectin, seromucoid, metalloproteinase-3 and CRP) and clinical and endoscopic activity of ulcerative colitis in children. Advances in Medical Sciences. 2020;65(2):259–64. DOI: https://doi.org/10.1016/j.advms.2020.03.004.
  56. Namaste SM, Aaron GJ, Varadhan R, Peerson JM, Suchdev PS; BRINDA Working Group. Methodologic approach for the biomarkers reflecting inflammation and nutritional determinants of anemia (BRINDA) project. The American Journal of Clinical Nutrition. 2017;106(1):333–47. DOI: https://doi.org/10.3945/ajcn.116.142273.
  57. Smith SA, Waters NJ. Pharmacokinetic and pharmacodynamic considerations for drugs binding to alpha-1-acid glycoprotein. Pharmaceutical Research. 2018;36(2):30. DOI: https://doi.org/10.1007/s11095-018-2551-x.
  58. Sproston NR, Ashworth JJ. Role of C-Reactive Protein at Sites of Inflammation and Infection. Frontiers in Immunology. 2018;9:754. DOI: https://doi.org/10.3389/fimmu.2018.00754.
  59. Lapic I, Padoan A, Bozzato D, Plebani M. Erythrocyte sedimentation rate and C-reactive protein in acute inflammation. American Journal of Clinical Pathology. 2020;153(1):14–29. DOI: https://doi.org/10.1093/ajcp/aqz142.
  60. Yao Z, Zhang Y, Wu H. Regulation of C-reactive protein conformation in inflammation. Inflammation Research. 2019;68(10):815–23. DOI: https://doi.org/10.1007/s00011-019-01269-1.
  61. Avan A, Tavakoly Sany SB, Ghayour-Mobarhan M, Rahimi HR, Tajfard M, Ferns G. Serum C-reactive protein in the prediction of cardiovascular diseases: Overview of the latest clinical studies and public health practice. Journal of Cellular Physiology. 2018;233(11):8508–25. DOI: https://doi.org/10.1002/jcp.26791.
  62. Li W, Cao T, Luo C, Cai J, Zhou X, Xiao X, Liu S. Crosstalk between ER stress, NLRP3 inflammasome, and inflammation. Applied Microbiology and Biotechnology. 2020;104(14):6129–40. DOI: https://doi.org/10.1007/s00253-020-10614-y.
  63. Wang J, Xia J, Yan X, Yang Y, Wei J, Xiong Y, Wu W, Liu Y, Chen Y, Jia B, Chen Z, Zhang Z, Ding W, Huang R, Wu C. The gamma-glutamyl transpeptidase to platelet ratio predicts liver inflammation in chronic hepatitis B with normal or mildly elevated alanine transaminase. Clinics and Research in Hepatology and Gastroenterology. 2020;44(6):913–22. DOI: https://doi.org/10.1016/j.clinre.2020.01.011.
  64. Ndrepepa G, Colleran R, Kastrati A. Gamma-glutamyl transferase and the risk of atherosclerosis and coronary heart disease. Clinica Chimica Acta. 2018;476:130–8. DOI: https://doi.org/10.1016/j.cca.2017.11.026.
  65. Mohi-Ud-Din R, Mir RH, Sawhney G, Dar MA, Bhat ZA. Possible pathways of hepatotoxicity caused by chemical agents. Сurrent drug metabolism. 2019;20(11):867–79. DOI: https://doi.org/10.2174/1389200220666191105121653.
  66. Jung SH, Lee W, Park SH, Lee KY, Choi YJ, Choi S, Kang D, Kim S, Chang TS, Hong SS, Lee BH. Diclofenac impairs autophagic flux via oxidative stress and lysosomal dysfunction: Implications for hepatotoxicity. Redox Biology. 2020;37:101751. DOI: https://doi.org/10.1016/j.redox.2020.101751.
  67. Vyas A, Purohit A, Ram H. Assessment of dose-dependent reproductive toxicity of diclofenac sodium in male rats. Drug and Chemical Toxicology. 2019;42(5):478–86. DOI: https://doi.org/10.1080/01480545.2017.1421659.
  68. Yeh JC, Wu CC, Choy CS, Chang SW, Liou JC, Chen KS, Tung TH, Lin WN, Hsieh CY, Ho CT, Wang TM, Chang JF. Non-Hepatic Alkaline Phosphatase, hs-CRP and Progression of Vertebral Fracture in Patients with Rheumatoid Arthritis: A Population-Based Longitudinal Study. Journal of Clinical Medicine. 2018;7(11):439. DOI: https://doi.org/10.3390/jcm7110439.
  69. Jo S, Han J, Lee YL, Yoon S, Lee J, Wang SE, Kim TH. Regulation of osteoblasts by alkaline phosphatase in ankylosing spondylitis. International Journal of Rheumatic Diseases. 2019;22(2):252–61. DOI: https://doi.org/10.1111/1756-185X.13419.
  70. Hirschmugl B, Crozier S, Matthews N, Kitzinger E, Klymiuk I, Inskip HM, Harvey NC, Cooper C, Sibley CP, Glazier J, Wadsack C, Godfrey KM, Desoye G, Lewis RM. Relation of placental alkaline phosphatase expression in human term placenta with maternal and offspring fat mass. International Journal of Obesity. 2018;42(6):1202–10. DOI: https://doi.org/10.1038/s41366-018-0136-8.
  71. Liao KP, Solomon DH. Lipids and cardiovascular risk through the lens of rheumatoid arthritis. Arthritis & Rheumatology. 2019;71(9):1393–5. DOI: https://doi.org/10.1002/art.40891.
  72. Kril IY, Gavrilyuk AM, Stoyka RS, Chop’yak VV, Kit YYa. Characteristics of enzymatic activity and protein composition of serum of rats under the conditions of immunization-induced inflammation of the joints. Experimental and clinical physiology and biochemistry. 2014;2:15–23. Ukrainian
  73. Hladkykh FV, Mikhailova ІP, Manchenko AO. Infusion of sodium and diclofenac with this combination with a cryopreserved placental extract on the lynchial balance in the syrovatous blood in experimental rheumatoid arthritis. Materials of the XXVII International Scientific and Practical Conference of Young Graduates and Students “Topical issues of new medicines development” (March 18–19, 2021); Kharkiv: National Pharmaceutical University of the Ministry of Health of Ukraine. 2021:272–3. Ukrainian

Supplementary files

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2. Figure 1 – Effect of DS and its combination with CPE on the level of TBA-AP in peripheral blood in rats with AA on the 28th day of the experiment

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3. Figure 2 – Effect of DS and its combination with CPE on the level of SOD in peripheral blood in rats with AA on the 28th day of the experiment

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4. Figure 3 – Effect of DS and its combination with CPE on the level of seromucoid in peripheral blood in rats with AA on the 28th day of the experiment

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5. Figure 4 – Effect of DS and its combination with CPE on the level of C-RP in peripheral blood in rats with AA on the 28th day of the experiment

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6. Figure 5 – Effect of DS and its combination with CPE on the level of alkaline phosphatase in peripheral blood in rats with AA on the 28th day of the experiment

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Copyright (c) 2021 Hladkykh F.V., Chyzh M.O., Manchenko A.O., Belochkina I.V., Mikhailova I.P.

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