Effect of Administration of Copper plasma Activated water and Anesthetic on Hematological and Pancreatic tissues of Wister rats

Main Article Content

Isaac John Umaru
Iseko Iyoko Kingsly
Prince Kwadwo Gyasi
Edom Favour Ogochukwu
Tensaba Andes Akafa
Jackson Soyinka Malantso
Bilyaminu Habibu
Kerenhappuch Isaac Umaru

Abstract

In biomedicine, applications of PAW span from biofilm removal, wound healing, deactivation of bacteria and viruses, dentistry (for teeth disinfection and whitening), and cancer therapy. The biochemical activity of PAW is derived from synergistic effects of the highly reactive species, specifically reactive oxygen and nitrogen species (RONS). PAW is considered a biofriendly and prospective solution for biotechnology applications due to the time dependent nature of its biochemical activity because of the active species, and its economic and environmental benefits of using air rather than toxic chemicals as the raw material. Thus, the study on Effect of Administration of Copper plasma Activated water and Anaesthetic on Haematological and Pancreatic tissues of Wister rats. Material and Methods: Preparation of plasma-activated water a non-thermal micro-hollow cathode discharge (MHCD) was used to generate plasma-activated waters (CU-PAWs). Results: The results showed the haematological profile of the animals treated with 400mgkg-' had a decrease in Haemoglobin, Mean capsular Haemoglobin (11.21 ± 1.23 and 22.93 ± 21.11) compared to the controlled group (15.03 ± 1.72 and 29.93 ± 7.27) and in animals treated with 200mgkg-1 and 400mgkg-1 there is a significant decrease in the platelets (21.96 ± 23.16 and 20.89 ± 24.03) compared to animals on control group (32.08± 16.70) (table 2). Animals treated with 200mgkg-' and 400mgkg-' have a decrease in platelet (22.36 ± 4.88 and 20.89 ± 24.03) compared to animals on control (32.08 ± 16.70) and also animals treated with 400mgkg-1 have an elevated white blood cell count 173-56 ± 4.50) compared to the control group (3.66 ± 3.06). Conclusion: Cupper plasma water is safe to be used since it do not have much effect on the blood biochemistry and haematological parameters unlike the aesthetic agents cause changes on the haematological and blood biochemistry parameters. Hence, it is important to be aware of the effects of these agents before using them in experiments.

Downloads

Download data is not yet available.

Scopus Citation Data

Data source Crossref
0
citations
Check Secondary Documents in Scopus
Open this article in Scopus, then check the Secondary documents tab. Use Manual Citation Fallback only for counts you have verified manually.
Open in Scopus
Similar Scopus Articles
Scopus
  1. Lukpanov R.E. (2027)
    Evaluation of the Effect of Additives on the Workability of Concrete Mix as Part of a Study of a Modified Wall Block
    Kompleksnoe Ispolzovanie Mineralnogo Syra, 342(3), 100-110
  2. Berenjian K. (2027)
    Impact of Mild Traumatic Brain Injury (mTBI) on CYP2D6 Activity and the Restorative Effects of Melatonin and Vitamin C Supplementation
    Iranian Journal of Pharmaceutical Research, 26(1)
  3. Achilova S.S. (2027)
    Activation of the mineralized mass of Central Kyzylkum using acidic wastewater from the oil and fat industry: Freundlich-based adsorption kinetics for fluorine release
    Kompleksnoe Ispolzovanie Mineralnogo Syra, 342(3), 65-79

Article Details

How to Cite
Umaru, I. J., Kingsly, I. I., Gyasi, P. K., Ogochukwu, E. F., Akafa, T. A., Malantso, J. S., Habibu, B., & Umaru, K. I. (2025). Effect of Administration of Copper plasma Activated water and Anesthetic on Hematological and Pancreatic tissues of Wister rats. African Journal of Biochemistry and Molecular Biology Research, 2(1), 1-19. https://doi.org/10.58578/ajbmbr.v2i1.4722

References

1. Zhou, Renwu, et al. "Plasma-activated water: Generation, origin of reactive species and biological applications." Journal of Physics D: Applied Physics 53.30 (2020): 303001.
2. R.D.; et al. Copper induces cell death by targeting lipoylated TCA cycle proteins. Science 2022, 375, 1254–1261.
3. Ruiz, L.M.; Libedinsky, A.; Elorza, A.A. Role of Copper on Mitochondrial Function and Metabolism. Front. Mol. Biosci. 2021, 8, 711227.
4. Festa, R.A.; Thiele, D.J. Copper: An essential metal in biology. Curr. Biol. CB 2011, 21, R877–R883. [CrossRef]
5. Novoselov, K.S.; Geim, A.K.; Morozov, S.V.; Jiang, D.; Zhang, Y.; Dubonos, S.V.; Grigorieva, I.V.; Firsov, A.A. Electric field effect inatomically thin carbon films. Science 2004, 306, 666–669. [CrossRef]
6. Nose, Y.; Wood, L.K.; Kim, B.E.; Prohaska, J.R.; Fry, R.S.; Spears, J.W.; Thiele, D.J. Ctr1 is an apical copper transporter in mammalian intestinal epithelial cells in vivo that is controlled at the level of protein stability. J. Biol. Chem. 2010, 285, 32385–32392. [CrossRef] [PubMed]
7. Xu, S.; Liu, D.; Chang, T.; Wen, X.; Ma, S.; Sun, G.; Wang, L.; Chen, S.; Xu, Y.; Zhang, H. Cuproptosis-Associated lncRNA Establishes New Prognostic Profile and Predicts Immunotherapy Response in Clear Cell Renal Cell Carcinoma. Front. Genet. 2022, 13, 938259. [CrossRef]
8. Greish, K.; Pittalà, V.; Taurin, S.; Taha, S.; Bahman, F.; Mathur, A.; Jasim, A.; Mohammed, F.; El-Deeb, I.M.; Fredericks, S.; et al. Curcumin-Copper Complex Nanoparticles for the Management of Triple-Negative Breast Cancer. Nanomaterials 2018, 8, 884. [CrossRef]
9. Hu, Y.; Qian, Y.; Wei, J.; Jin, T.; Kong, X.; Cao, H.; Ding, K. The Disulfiram/Copper Complex Induces Autophagic Cell Death in Colorectal Cancer by Targeting ULK1. Front. Pharmacol. 2021, 12, 752825. [CrossRef] [PubMed]
10. Li, H.; Wang, J.; Wu, C.; Wang, L.; Chen, Z.S.; Cui, W. The combination of disulfiram and copper for cancer treatment. Drug Discov. Today 2020, 25, 1099–1108. [CrossRef] [PubMed]39
11. Shao, T.; Zhang, C.;Wang, R.X.; Yan, P.; Ren, C.Y. Atmospheric-pressure Pulsed Gas Discharge and Pulsed Plasma Application. High Volt. Eng. 2016, 42, 685–705.
12. Tresp, H.; Hammer, M.U.; Winter, J.; Weltmann, K.D.; Reuter, S. Quantitative detection of plasma-generated radicals in liquids by electron paramagnetic resonance spectroscopy. J. Phys. D Appl. Phys. 2013, 46, 435401. [CrossRef]
13. Xu, D.; Liu, D.;Wang, B.; Chen, C.; Kong, M.G. In Situ OH Generation from O2 and H2 O2 Plays a Critical Role in Plasma-Induced Cell Death. PLoS ONE 2015, 10, e0128205.
14. Pavlovich, M.J.; Chang, H.W.; Sakiyama, Y.; Clark, D.S.; Graves, D.B. Ozone correlates with antibacterial effects from indirect air dielectric barrier discharge treatment of water. J. Phys. D Appl. Phys. 2013, 46, 145202. [CrossRef]
15. Wende, K.; Williams, P.; Dalluge, J.; Van Gaens, W.; Aboubakr, H.; Bischof, J.; Von Woedtke, T.; Goyal, S.M.; Weltmann, K.D.; Bogaerts, A. Identification of the biologically active liquid chemistry induced by a nonthermal atmospheric pressure plasma jet. Biointerphases 2015, 10, 29518–103307. [CrossRef] [PubMed]
16. Yan, X.; Xiong, Z.; Zou, F.; Zhao, S.; Lu, X.; Yang, G.; He, G.; Ostrikov, K.K. Plasma-Induced Death of HepG2 Cancer Cells: Intracellular Effects of Reactive Species. Plasma Process. Polym. 2012, 9, 59–66. [CrossRef]
17. Liu, D.X.; Liu, Z.C.; Chen, C.; Yang, A.J.; Li, D.; Rong, M.Z.; Chen, H.L.; Kong, M.G. Aqueous reactive species induced by a surface air discharge: Heterogeneous mass transfer and liquid chemistry pathways. Sci. Rep. 2016, 6, 23737. [CrossRef] [PubMed]
18. Chen TP, Su TL, Liang JF (2017) Plasma-activated solutions for bacteria and biofilm inactivation. Curr Bioact Compd 13(1):59–65
19. Alves, H. C., Valentim, A. M., Olsson, I. A. and Antunes, L. M. 2007. Intraperitoneal propofol and propofol fentanyl, sufentanil and remifentanil combinations for mouse anaesthesia. Lab. Anim. 41: 329–336. [Medline] [CrossRef]
20. Kale, V. P., Joshi, G. S., Gohil, P. B. and Jain, M. R. 2009. Effect of fasting duration on clinical pathology results in Wistar rats. Vet. Clin. Pathol. 38: 361–366.
21. Maejima, K. and Nagase, S. 1991. Effect of starvation and refeeding on the circadian rhythms of hematological and clinico-biochemical values, and water intake of rats. Jikken Dobutsu 40: 389–393.
22. Matsuzawa, T. and Sakazume, M. 1994. Effects of fasting on haematology and clinical chemistry values in the rat and dog. Comp. Haem. Inter. 4:152–156.
23. Sherif, M. S., Anis, M. Z., Sahar, H. O., Khaled, M. S. and Wafaa, A. H. 2015. Effect of Intermittent Fasting on Brain Neurotransmitters, Neutrophils Phagocytic Activity, and Histopathological Finding in Some Organs in Rats. Inter. J. Res. Stu. Bio 3: 38–45
24. Apostolou, A., Saidt, L. and Brown, W. R. 1976. Effect of overnight fasting of young rats on water consumption, body weight, blood sampling, and blood composition. Lab. Anim. Sci. 26: 959–960
25. Bekkevold, C. M., Robertson, K. L., Reinhard, M. K., Battles, A. H. and Rowland, N. E. 2013. Dehydration parameters and standards for laboratory mice. J. Am. Assoc. Lab. Anim. Sci. 52: 233–239.
26. Kale, V. P., Joshi, G. S., Gohil, P. B. and Jain, M. R. 2009. Effect of fasting duration on clinical pathology results in Wistar rats. Vet. Clin. Pathol.38: 361–366
27. Maejima, K. and Nagase, S. 1991. Effect of starvation and refeeding on the circadian rhythms of hematological and clinico-biochemical values, and water intake of rats. Jikken Dobutsu 40: 389–393.
28. Matsuzawa, T. and Sakazume, M. 1994. Effects of fasting on haematology and clinical chemistry values in the rat and dog. Comp. Haem. Inter. 4: 152–156.
29. Sherif, M. S., Anis, M. Z., Sahar, H. O., Khaled, M. S. and Wafaa, A. H. 2015. Effect of Intermittent Fasting on Brain Neurotransmitters, Neutrophils Phagocytic Activity, and Histopathological Finding in Some Organs in Rats. Inter. J. Res. Stu. Bio 3: 38–45
30. Thompson, C. S., Mikhailidis, D. P., Jeremy, J. Y., Bell, J. L. and Dandona, P. 1987. Effect of starvation on biochemical indices of renal function in the rat. Br. J. Exp. Pathol. 68: 767–775.
31. Asakawa, K., Hizuka, N., Takano, K., Horikawa, R., Sukegawa, I., Demura, H. and Shizume, K. 1992. Effects of insulin-like growth factor I or human growth hormone in fasted rats. Growth Regul. 2: 40–44.
32. Kale, V. P., Joshi, G. S., Gohil, P. B. and Jain, M. R. 2009. Effect of fasting duration on clinical pathology results in Wistar rats. Vet. Clin. Pathol. 38: 361–366
33. Maejima, K. and Nagase, S. 1991. Effect of starvation and refeeding on the circadian rhythms of hematological and clinico-biochemical values, and,water intake of rats. Jikken Dobutsu 40: 389–393
34. Kirihara, Y., Takechi, M., Kurosaki, K., Kobayashi, Y., Saito, Y. and Takeuchi, T. 2016. Effects of an anesthetic mixture of medetomidine, midazolam, and butorphanol in rats-strain difference and antagonism by atipamezole. Exp. Anim. 65: 27–36.
35. Arakawa, H., Matumoto, H. and Katou, T. 2012. Neuroleptoanalgesia using a drug combination of medetomidine, midazolam, and butorphanol in mice. J. Exp. Anim. Tech. 47: 65–72.
36. Arras, M., Autenried, P., Rettich, A., Spaeni, D. and Rülicke, T. 2001. Optimization of intraperitoneal injection anesthesia in mice: drugs, dosages, adverse effects, and anesthesia depth. Comp. Med. 51: 443–456.
37. Dubin, S. 1999. Uses of a biocompatible adhesive paste to improve the performance of rodent anesthesia face masks. Lab. Anim. 28: 50–51.
38. Hayashi, K., Nishimura, R., Yamaki, A., Kim, H., Matsunaga, S., Sasaki, N. and Takeuchi, A. 1994. Comparison of sedative effects induced by medetomidine, medetomidine-midazolam and medetomidine-butorphanol in dogs. J. Vet. Med. Sci. 56: 951–956
39. Kazunori, K., Shinji, H., Koji, I., Hironori, M., Hirokazu, F., Mami, F. and Hiromasa, T. 2012. Evaluation of the combination of three anesthetics in rats and rabbits. Annual Report of Hatano Research Institute 35: 53–59.
40. Ochiai, Y., Iwano, H., Sakamoto, T., Hirabayashi, M., Kaneko, E., Watanabe, T., Yamashita, K. and Yokota, H. 2016. Blood biochemical changes in mice after administration of a mixture of three anesthetic agents. J. Vet. Med. Sci. 78: 951–956.
41. Ranheim, B., Horsberg, T. E., Søli, N. E., Ryeng, K. A. and Arnemo, J. M. 2000. The effects of medetomidine and its reversal with atipamezole on plasma glucose, cortisol and noradrenaline in cattle and sheep. J. Vet. Pharmacol. Ther. 23: 379–387.
42. Venn, R. M., Bryant, A., Hall, G. M. and Grounds, R. M. 2001. Effects of dexmedetomidine on adrenocortical function, and the cardiovascular, endocrine and inflammatory responses in post-operative patients needing sedation in the intensive care unit. Br. J. Anaesth. 86: 650–656.
43. Zuurbier, C. J., Emons, V. M. and Ince, C. 2002. Hemodynamics of anesthetized ventilated mouse models: aspects of anesthetics, fluid support, and strain. Am. J. Physiol. Heart Circ. Physiol. 282: H2099–H2105
44. Zuurbier, C. J., Koeman, A., Houten, S. M., Hollmann, M. W. and Florijn, W. J. 2014. Optimizing anesthetic regimen for surgery in mice through
45. minimization of hemodynamic, metabolic, and inflammatory perturbations. Exp. Biol. Med. (Maywood) 239: 737–746
46. Ambrisko, T. D. and Hikasa, Y. 2003. The antagonistic effects of atipamezole and yohimbine on stress-related neurohormonal and metabolic responses induced by medetomidine in dogs. Can. J. Vet. Res. 67: 64–67.
47. Angel, I., Bidet, S. and Langer, S. Z. 1988. Pharmacological characterization of the hyperglycemia induced by alpha-2 adrenoceptor agonists. J. Pharmacol. Exp. Ther. 246: 1098–1103

Explore Our Journals
Find the most suitable journal for your research. If this journal does not fully align with the scope of your manuscript, we invite you to explore our wider portfolio of journals covering diverse fields of study. Please select one of the journals below to identify the most appropriate publication platform for your work.

Most read articles by the same author(s)

1 2 3 4 5 6 7 8 9 10 > >>