The Measurement of Activity of the Ca2+_Mg2+ ATPase in Membranous Vesicles Isolated from Smooth Muscle of Ileum in Rats Treated with Ultraviolet Radiation

Authors

  • Khalid H. Gathwan Basic Science, College of Dentistry, University of Baghdad, 10071 Baghdad, IRAQ.
  • Ahmed Anwar Albir Basic Science, College of Dentistry, University of Baghdad, 10071 Baghdad, IRAQ.
  • Salim J. Attia Basic Science, College of Dentistry, University of Baghdad, 10071 Baghdad, IRAQ. https://orcid.org/0000-0001-7521-0115

DOI:

https://doi.org/10.23851/mjs.v34i3.1326

Keywords:

Ca2 _Mg2 ATPase, Rats, Ultraviolet radiation

Abstract

The Ca2+_Mg2+ ATPase are high attraction calcium pump, that contributes in maintaining plasma membrane of cytoplasm Ca2+, Mg2+ homeostasis by source to the outside of cell. The aim of the study is to evaluate the effect of the ultraviolet radiation on the activity of the Ca2+_Mg2+ ATPase in the membranous vesicles of ileum in rats. Thirty adult Sprague–Dawley rats (age, 3-4 months, weight range, 180 – 200 g) were used in this experiment, which divided in to 5 groups (n = 6 / group). The membrane vesicles isolated from smooth muscles of rats showed high activity Ca2+_Mg2+ ATPase. All isolated membranous vesicles are irradiated with Ultraviolet radiation of 250 nanometers except control group. The irradiation period for each group was (5, 10, 30 and 45) minutes, respectively. The activity of Ca2+_Mg2+ ATPase was decreased with increased time of irradiation. In conclusion, the increased time of irradiation inhibited Ca2+_Mg2+ ATPase activity isolated from ileum smooth muscles of rats. The recommendations are to expose other organs like liver and kidney to UV radiation to explain its effect or using other range of UV radiation to reflect its effect.

Downloads

Download data is not yet available.

References

Matthew A., Shmygol A. and Wray S. (2004). Ca2+ entry, efflux and release in smooth muscle, Biol Res 37: 617-624.

CrossRef | PubMed

Jack A., (2022). Discovery of the regulatory role of calcium ion in muscle contraction andrelaxation: Setsuro Ebashi and the international emergence of Japanese muscle research, Adv Physiol Educ, 46(3): 481-490.

CrossRef | PubMed

Bradley S. and George S., (2000). Effects of Mg2+ on Ca2+ release from sarcoplasmic reticulum of skeletal muscle fibres from yabby (crustacean) and rat, J Physiol., 526(2):299-312.

CrossRef | PubMed

Deshpande L., Delorenzo R., (2020). Novel therapeutics for treating organophosphate-induced status epilepticus co-morbidities, based on changes in calcium homeostasis, Neurobiol Dis., 133:104418.

CrossRef | PubMed

Choi H., and Lee C., (2016). Time-course change of hippocalcin expression in the mouse hippocampus following pilocarpine-induced status epilepticus, J. Vet. Sci.17:137-144.

CrossRef | PubMed

Umar S., Shahid N., Nazar L., Tanveer M., Devya G., Archoo S., (2021). Pharmacological Activation of Autophagy Restores Cellular Homeostasis in Ultraviolet-(B)-Induced Skin Photodamage, Front. Oncol., 11, 726066.

CrossRef | PubMed

Berridge, M., Lipp P., Bootman M., (2000). The Versatility and universality of calcium signalling. Nat. Rev. Mol. Cell Biol. 1, 11-21.

CrossRef | PubMed

Brini M., Cali T., Ottolini D., Carafoli E. (2013). The plasma membrane calcium pump in health and disease. FEBS J. 280, 5385-5387.

CrossRef | PubMed

Brini M., (2009). Plasm membrane Ca2+- ATPase: from a housekeeping function to a versatile signaling role. Pflugers Arch-Eur. J. Physiol. 457, 657-664.

CrossRef | PubMed

Joachim K., (2022). Structure, Function and Regulation of the Plasma Membrane Calcium Pump in Health and Disease, Int. J. Mol. Sci. 2022, 23(3), 1027;

CrossRef | PubMed

Wenjuan D., Juefei Z., Wei L., Teng Z., Qianqian C., Fuyu Y., Taotao W., (2013), Plasma membrane calcium ATPase 4b inhibits nitric oxide generation through calcium-induced dynamic interaction with neuronal nitric oxide synthase, Protein & Cell, 4(4):286-298.

CrossRef | PubMed

Deshpande L., Delorenzo .J., Chrun S., and Parson J., (2020). Neural- specific inhibition of endoplasmic reticulum Mg -Ca ATPase uptake in a mixed primary hippocampal culture model, Brain. Scin. 10(7),438.

CrossRef | PubMed

Otilia G., Ioana M., Iulia P., Stefania D., Ramona P., Mioara C., Roxana B., Madalina C. and Sorin C., (2023), In Vitro Assessment of the Impact of Ultraviolet B Radiation on Oral Healthy and Tumor Cells, Photonics, 10(4), 464;

CrossRef

Zsófia S., Zsuzsanna N., József B., Györgyi K., Péter N.,Erika S., György T., Rosanna P. and Brahim S., (2023), Assessment of Inflammation in 3D Reconstructed Human Skin Exposed to Combined Exposure to Ultraviolet and Wi-Fi Radiation, Int. J. Mol. Sci., 24(3), 2853;

CrossRef | PubMed

Orazio J., Jarret S., Amero A. and Scot T., (2013). UVradiationand skin. Int. J. Mol. Sci. 14, 12222-12248.

CrossRef | PubMed

Hoeijmakers, J., (2009). DNA damage, aging and cancer, J. Med. 361, 1475-1485.

CrossRef | PubMed

Naraman, D.L.; Saladi,R.N.and Fox, J. L. (2010). Ultraviolet radiation and skin cancer, Int. J. Dermatol. 49, 978-986.

CrossRef | PubMed

Ahmed U., Abdulla T., (2022). Ozone Layer Depletion and Emerging Public Health Concerns - An Update on Epidemiological Perspective of the Ambivalent Effects of Ultraviolet Radiation Exposure, Front. Oncol., 12, 866733.

CrossRef | PubMed

Kim J, Andrew T. (2020). Real-time and noninvasive detection of UV-Induced deep tissue damage using electrical tattoos. Biosens Bioelectron. 15, 150: 111909.

CrossRef | PubMed

Zhongwei L. and Raouf A., (2018). Evolving Mechanisms of Vascular Smooth Muscle Contraction Highlight Key Targets in Vascular Disease, Biochem Pharmacol. 153: 91-122.

CrossRef | PubMed

Sanders K., (2008). Regulation of smooth muscle excitation and contraction, Neurogastroenterol Motil., 20 (Suppl 1): 39-53.

CrossRef | PubMed

Michael C., Neil H. and Cheryl A., (2021). Centrifugation Removes a Population of Large Vesicles, or "Macroparticles," Intermediate in Size to RBCs and Microvesicles, Int J Mol Sci., 22(3): 1243.

CrossRef | PubMed

Wu Q, Guo D, Bi H, Wang D, Du Y. (2013), UVB irradiation-induced dysregulation of plasma membrane calcium ATPase1 and intracellular calcium homeostasis in human lens epithelial cells. Mol Cell Biochem. 382(1-2):263-272.

CrossRef | PubMed

Kazi M., Kamrul H., Sufara A., Renu T., Narendra T., (2013), Global calcium transducer P-type Ca2+-ATPases open new avenues for agriculture by regulating stress signalling, Journal of Experimental Botany, 64(11):3099-3109.

CrossRef | PubMed

Tatalovich Z., Wilson J., Mack T., (2006). The objective assessment of lifetime cumulative ultraviolet exposure of determining melanoma risk, J. Photochem. photo. Biol. 85, 198-204.

CrossRef | PubMed

Balasubramanian D., (2000). Ultraviolet radiation and contaract, J. Ocul. Phamacol. Ther. 16:285-297.

CrossRef | PubMed

Lccas R., McMichael A., Armstrong B., (2008). Estimating the global disease burden due to Ultraviolet radiation exposure, Int. J. Epidemoil. 37,654-667.

CrossRef | PubMed

Brozyna A., Zbytek B., Granese J., Carlson J., Ross j., (2007), Mechanism of UV-related carcinogenesis and its contribution to nevi/melanoma, Expert Rev Dermatol. 2(4):451-469.

CrossRef | PubMed

Downloads

Key Dates

Published

30-09-2023

Issue

Section

Original Article

How to Cite

[1]
K. H. . Gathwan, A. A. . Albir, and S. J. Attia, “The Measurement of Activity of the Ca2+_Mg2+ ATPase in Membranous Vesicles Isolated from Smooth Muscle of Ileum in Rats Treated with Ultraviolet Radiation”, Al-Mustansiriyah J. Sci., vol. 34, no. 3, pp. 10–14, Sep. 2023, doi: 10.23851/mjs.v34i3.1326.

Similar Articles

1-10 of 38

You may also start an advanced similarity search for this article.