العلاقة بين سمية الفلوريد والإجهاد التأكسدي ومضاعفات الحمل لدى النساء اللواتي يعشن في مناطق التسمم بالفلور
محتوى المقالة الرئيسي
الملخص
كان الهدف من هذه الدراسة هو التحقيق من العلاقة بين مستويات فلوريد البلازما المرتفعة، والإجهاد التأكسدي، ومضاعفات الحمل (الإجهاض، وموت الجنين داخل الرحم، والولادة المبكرة، وتسمم الحمل) لدى النساء اللواتي يعشن في إقليم سطات بالمغرب. تم جمع عينات الدم من النساء الحوامل ذوات الحمل الطبيعي (عدد = 60)، والإجهاض (عدد = 20)، وموت الجنين داخل الرحم (عدد = 10)، والولادة المبكرة (عدد = 20)، وتسمم الحمل (عدد = 20). بعد ذلك، تم تحديد مستويات فلوريد البلازما والأنشطة الأنزيمية لخلايا الدم الحمراء من superoxide dismutase (SOD)، catalase (CAT)، glutathione peroxidase (GPx). أظهرت النتائج أن مستويات الفلوريد في البلازما أقل بشكل ملحوظ عند النساء ذوات الحمل الطبيعي بتركيز 0.030 ± 0.003 ملغم / لتر مقارنة بالنساء اللائي تعرضن للإجهاض وموت الجنين داخل الرحم والولادة المبكرة وتسمم الحمل، بتركيزات 0.040 ± 0.002، 0.037 ± 0.002، 0.034 ± 0.004 و0.034 ± 0.003 ملغم / لتر، على التوالي. بالإضافة إلى ذلك، زاد نشاط SOD بشكل ملحوظ عند النساء اللواتي يعانين من مضاعفات الحمل، بينما انخفضت أنشطة CAT وGPx مقارنة بالنساء ذوات الحمل الطبيعي. علاوة على ذلك، لوحظ وجود علاقة قوية بين مستويات فلوريد البلازما وأنشطة مضادات الأكسدة ومضاعفات الحمل. قد يؤدي وجود مستويات عالية من فلوريد البلازما إلى زيادة انتشار الإجهاض ووفاة الجنين داخل الرحم والولادة المبكرة وتسمم الحمل، عبر مسار الإجهاد التأكسدي لدى النساء الحوامل اللواتي يعشن في إقليم سطات بالمغرب.
Received 28/12/2022
Revised 20/06/2023
Accepted 22/06/2023
Published Online First 20/09/2023
تفاصيل المقالة

هذا العمل مرخص بموجب Creative Commons Attribution 4.0 International License.
كيفية الاقتباس
المراجع
Moreno-Fernandez J, Ochoa JJ, Lopez-Frias M, Diaz-Castro J. Impact of early nutrition, physical activity and sleep on the fetal programming of disease in the pregnancy: a narrative review. Nutrients. 2020; 12(12): 3900. https://doi.org/10.3390/nu12123900
Hamza MA. Lymphocytes Prediction of Homeostasis Model Assessment of Beta-cells Function (HOMA-B) and C-peptide Level during Pregnancy: New Insight into Beta-cells Proliferation and Insulin Sensitivity. Baghdad Sci J. 2022; 19(4): 0821. https://orcid.org/0000-0001-7935-9734
Farhan LO, Mustafa SA, Mubder NS. Effect of Pregnancy on Selenium, Cupper, Zinc and Others Biochemical Feacture. Baghdad Sci J . 2013; 10(4): 1182-1189.https://doi.org/10.21123/bsj.2013.10.4.1182-1189
Bouchab H, Ishaq A, El Kebbaj R, Nasser B, Saretzki G. Protective effect of argan oil on DNA damage in vivo and in vitro. Biomarkers. 2021; 26(5): 425-3. https://doi.org/10.1080/1354750x.2021.1905068
Simon Szabo Z, Fogarasi E, Nemes Nagy E, Denes L, Croitoru M, Szabo B. Oxidative stress and peripartum outcomes. Exp Ther Med. 2021; 22(1): 1-6. https://doi.org/10.3892%2Fetm.2021.10203
Pei J, Zhao S, Yin M, Wu F, Li J, Zhang G, et al. Differential proteomics of placentas reveals metabolic disturbance and oxidative damage participate yak spontaneous miscarriage during late pregnancy. BMC Vet Res. 2022; 18(1): 1-5. https://doi.org/10.1186/s12917-022-03354-w
Chiarello DI, Abad C, Rojas D, Toledo F, Vázquez CM, Mate A, et al. Oxidative stress: Normal pregnancy versus preeclampsia. Biochim Biophys Acta Mol Basis Dis. 2020; 1866(2): 165354. https://doi.org/10.1016/j.bbadis.2018.12.005
Angwa LM, Jiang Y, Pei J, Sun D. Antioxidant phytochemicals for the prevention of fluoride-induced oxidative stress and apoptosis: A review. Biol Trace Elem Res. 2022; 200(3): 1418-41. https://doi.org/10.1007/s12011-021-02729-8
Kampouri M, Gustin K, Stråvik M, Barman M, Levi M, Daraki V, et al. Association of maternal urinary fluoride concentrations during pregnancy with size at birth and the potential mediation effect by maternal thyroid hormones: The Swedish NICE birth cohort. Environ Res. 2022; 214: 114129. https://doi.org/10.1016/j.envres.2022.114129
Ortíz-García SG, Torres-Sánchez LE, Muñoz-Rocha TV, Mercado-García A, Peterson KE, Hu H, et al. Maternal urinary fluoride during pregnancy and birth weight and length: Results from ELEMENT cohort study. Sci Total Environ. 2022; 156459. https://doi.org/10.1016/j.scitotenv.2022.156459
El Amiri B, Rahim A, Sibaoueih M. Perception and farming practices to mitigate fluorosis in sheep in three communes of the province of KhouribgaMorocco. Afr Medit Agric J. 2022; 133:1-17. https://doi.org/10.34874/imist.prsm/afrimed-i133.30678
Aksoy M, Küfrevioglu I. Inhibition of human erythrocyte glutathione S-transferase by some flavonoid derivatives. Toxin Rev. 2017; 37(3): 251–257. https://doi.org/10.1080/15569543.2017.1345945
Lowry OH. Protein measurement with the Folin phenol reagent. J biol Chem. 1951; 193: 265-275. https://doi.org/10.1016/S0021-9258(19)52451-6
Beyer WF, Fridovich I. Assaying for superoxide dismutase activity: some large consequences of minor changes in conditions. Anal Biochem. 1987; 161(2): 559-66. https://doi.org/10.1016/0003-2697(87)90489-1
Babitha MP, Bhat SG, Prakash HS, Shetty HS. Differential induction of superoxide dismutase in downy mildew‐resistant and‐susceptible genotypes of pearl millet. Plant Pathol. 2002; 51(4): 480-6. https://doi.org/10.1046/j.1365-3059.2002.00733.x
Ni J, Sasaki Y, Tokuyama S, Sogabe A, Tahara Y. Conversion of a typical catalase from Bacillus sp. TE124 to a catalase-peroxidase by directed evolution. J Biosci Bioeng. 2002; 93(1): 31-6. https://doi.org/10.1016/S1389-1723(02)80050-0
Flohé L, Günzler WA. Assays of glutathione peroxidase. InMethods in enzymology. Academic Press.1984; 105: 114-121. https://doi.org/10.1016/s0076-6879(84)05015-1
Opydo-Szymaczek J, Borysewicz-Lewicka M. Variations in concentration of fluoride in blood plasma of pregnant women and their possible consequences for amelogenesis in a fetus. Homo. 2006; 57(4): 295-307. https://doi.org/10.1016/j.jchb.2006.02.002
Thomas DB, Basu N, Martinez-Mier EA, Sánchez BN, Zhang Z, Liu Y, et al. Urinary and plasma fluoride levels in pregnant women from Mexico City. Environ Res. 2016; 150: 489-95. https://doi.org/10.1016/j.envres.2016.06.046
Njau M, Mujuni F, Chibwe E, Kiritta R, Matovelo D. Hypocalcemia In Pregnancy: Diagnosis Challenges In Low Resource Settings. J Med Case Rep Case Series. 2022; 3(05). Https://Doi.Org/10.38207/JMCRCS/2022/MAY03050133
Mallott EK, Borries C, Koenig A, Amato KR, Lu A. Reproductive hormones mediate changes in the gut microbiome during pregnancy and lactation in Phayre’s leaf monkeys. Sci Rep. 2020; 10(1): 9961. https://doi.org/10.1038/s41598-020-66865-2
Ferreira MK, Aragão WA, Bittencourt LO, Puty B, Dionizio A, de Souza MP, et al. Fluoride exposure during pregnancy and lactation triggers oxidative stress and molecular changes in hippocampus of offspring rats. Ecotoxicol Environ Saf. 2021; 208: 111437. https://doi.org/10.1016/j.ecoenv.2020.111437
Souza-Monteiro D, Ferreira MK, Bittencourt LO, Aragão WA, Oliveira IG, Maia CS, et al. Intrauterine and postnatal exposure to high levels of fluoride is associated with motor impairments, oxidative stress, and morphological damage in the cerebellum of offspring rats. Int J Mol Sci. 2022; 23(15): 8556. https://doi.org/10.3390/ijms23158556
Rahim A, Essamadi A, El Amiri B. Endemic fluorosis in ruminants and its socioeconomic impact in Morocco. Afr Medit Agric J. 2023.138: 77-95. https://doi.org/10.34874/imist.prsm/afrimed-i138.39131
Thippeswamy HM, Kumar MN, Girish M, Prashanth SN, Shanbhog R. Linear regression approach for predicting fluoride concentrations in maternal serum, urine and cord blood of pregnant women consuming fluoride containing drinking water. Clin Epidemiol Glob Health. 2021; 10: 100685. https://doi.org/10.1016/j.cegh.2020.100685
Goyal LD, Bakshi DK, Arora JK, Manchanda A, Singh P. Assessment of fluoride levels during pregnancy and its association with early adverse pregnancy outcomes. J Family Med Prim Care. 2020; 9(6): 2693. https://doi.org/10.4103%2Fjfmpc.jfmpc_213_20
de Lucca L, Jantsch LB, Vendrame SA, de Paula HL, dos Santos Stein C, Gallarreta FM, et al. Variation of the Oxidative Profile in Pregnant Women With and Without Gestational Complications. Matern Child Health J. 2022; 26(10): 2155-68. https://doi.org/10.1007/s10995-022-03475-6
San Juan-Reyes S, Gómez-Oliván LM, Islas-Flores H, Dublán-García O. Oxidative stress in pregnancy complicated by preeclampsia. Arch Biochem Biophys. 2020; 681: 108255. https://doi.org/10.1016/j.abb.2020.108255
Ferreira RC, Fragoso MB, Bueno NB, Goulart MO, de Oliveira AC. Oxidative stress markers in preeclamptic placentas: A systematic review with meta-analysis. Placenta. 2020; 99: 89-100. https://doi.org/10.1016/j.placenta.2020.07.023
Bharadwaj S, Bhat VB, Vickneswaran V, Adhisivam B, Zachariah B, Habeebullah S. Oxidative stress in preeclamptic mother–newborn dyads and its correlation with early neonatal outcome–a case control study. J Matern -Fetal Neonatal Med. 2018; 31(12): 1548-53. https://doi.org/10.1080/14767058.2017.1319933
Ahmad IM, Zimmerman MC, Moore TA. Oxidative stress in early pregnancy and the risk of preeclampsia. Pregnancy Hypertens. 2019; 18: 99-102. https://doi.org/10.1016%2Fj.preghy.2019.09.014
Drejza MA, Rylewicz K, Majcherek E, Gross-Tyrkin K, Mizgier M, Plagens-Rotman K, et al. Markers of Oxidative Stress in Obstetrics and Gynaecology—A Systematic Literature Review. Antioxidants. 2022; 11(8): 1477. https://doi.org/10.3390/antiox11081477
Rahim A, Aydogmus-Öztürk F, Cakir C, Essamadi A, El Amiri B. Mitigating Fluoride, Lead, Arsenic and Cadmium Toxicities in Laboratory Animals and Ruminants through Natural Products. Rec Agric Food Chem. 2022; 2: 1–17. http://doi.org/10.25135/rfac.6.2202.2365
Cook FJ, Seagrove-Guffey M, Mumm S, Veis DJ, McAlister WH, Bijanki VN, et al. Non-endemic skeletal fluorosis: causes and associated secondary hyperparathyroidism (case report and literature review). Bone. 2021; 145: 115839. https://doi.org/10.1016/j.bone.2021.115839
Haroon M, Zubair H, Mudassir AQ, Perveen S, Fatima A. Incidence of Hypocalcemia in Women Suffering from Preeclampsia. Pak J Med Sci. 2022; 16(04): 356-357. https://doi.org/10.53350/pjmhs22164356
Zhao H, Zhu Y, Zhao Y, Wang T, Li H, Yang J, et al. Alleviating effects of selenium on fluoride-induced testosterone synthesis disorder and reproduction toxicity in rats. Ecotoxicol Environ Saf. 2022;247:114249. https://doi.org/10.1016/j.ecoenv.2022.114249
Radovanović J, Antonijević B, Kolarević S, Milutinović-Smiljanić S, Mandić J, Vuković-Gačić B, et al. Genotoxicity of fluoride subacute exposure in rats and selenium intervention. Chemosphere. 2021; 266: 128978. https://doi.org/10.1016/j.chemosphere.2020.128978
Rahim A, Essamadi A, El Amiri B. A comprehensive review on endemic and experimental fluorosis in sheep: Its diverse effects and prevention. Toxicology. 2022; 465: 153025. https://doi.org/10.1016/j.tox.2021.153025.
Menon R. Oxidative stress damage as a detrimental factor in preterm birth pathology. Front immunol. 2014 ;5 : 567. https://doi.org/10.3389/fimmu.2014.00567
Toboła-Wróbel K, Pietryga M, Dydowicz P, Napierała M, Brązert J, Florek E. Association of oxidative stress on pregnancy. Oxid Med Cell Longev. 2020; 2020. https://doi.org/10.1155/2020/6398520