Direct Effects of Waterpipe Smoke Extract on Aortic Endothelial Cells: An In Vitro Study
Language English Country Czech Republic Media print
Document type Journal Article
PubMed
40126144
PubMed Central
PMC11995937
DOI
10.33549/physiolres.935409
PII: 935409
Knihovny.cz E-resources
- MeSH
- Aorta * drug effects metabolism cytology pathology MeSH
- Apoptosis drug effects MeSH
- Cell Line MeSH
- Endothelial Cells * drug effects metabolism pathology MeSH
- Smoke * adverse effects MeSH
- Water Pipe Smoking * adverse effects MeSH
- Humans MeSH
- Oxidative Stress drug effects physiology MeSH
- Cell Survival drug effects physiology MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Smoke * MeSH
Waterpipe smoking (WPS) has adverse health effects that include endothelial dysfunction with mechanisms involving oxidative stress and inflammation. Nonetheless, there is a scarcity of data on the direct impact of WPS on endothelial function. In this study, we assessed the in vitro effects of waterpipe smoke extract (WPSE) on aortic endothelial cell lines, namely the TeloHAEC. The WPSE markedly caused concentration- and time-dependent decreases in cellular viability. When compared with the control, at a concentration of 20 % and an incubation period of 48 h, the WPSE significantly increased the levels of lactate dehydrogenase, and markers of oxidative stress including thiobarbituric acid reactive substances, superoxide dismutase, catalase, and reduced glutathione. Moreover, the concentrations of proinflammatory cytokine (tumor necrosis factor alpha), and adhesion molecules (E-selectin and intercellular adhesion molecule-1) were also significantly augmented. Likewise, WPSE triggered mitochondrial dysfunction, DNA oxidative damage, as well as apoptosis in TeloHAEC cells. Similarly, cells cultured with WPSE have shown increased expression of phosphorylated nuclear factor-kappaB and hypoxia-inducible factor 1-alpha (HIF-1alpha). In conclusion, our study showed that WPSE triggers endothelial inflammation, oxidative stress, DNA damage, mitochondrial dysfunction, and apoptosis via mechanisms involving the activation of nuclear factor-kappaB and HIF-1alpha. Key words Waterpipe smoking, Aortic endothelial cells, Inflammation, Oxidative Stress.
See more in PubMed
Taati B, Arazi H, Suzuki K. Oxidative Stress and Inflammation Induced by Waterpipe Tobacco Smoking Despite Possible Protective Effects of Exercise Training: A Review of the Literature. Antioxidants (Basel) 2020;9:777. doi: 10.3390/antiox9090777. PubMed DOI PMC
Shihadeh A. Investigation of mainstream smoke aerosol of the argileh water pipe. Food Chem Toxicol. 2003;41:143–152. doi: 10.1016/S0278-6915(02)00220-X. PubMed DOI
Maziak W, Ben Taleb Z, Jawad M, Afifi R, Nakkash R, Akl EA, Ward KD, et al. Consensus statement on assessment of waterpipe smoking in epidemiological studies. Tob Control. 2017;26:338–343. doi: 10.1136/tobaccocontrol-2016-052958. PubMed DOI PMC
Nemmar A, Al-Salam S, Beegam S, Yuvaraju P, Ali BH. Gum Arabic Ameliorates Impaired Coagulation and Cardiotoxicity Induced by Water-Pipe Smoke Exposure in Mice. Front Physiol. 2019;10:53. doi: 10.3389/fphys.2019.00053. PubMed DOI PMC
Al Ali R, Vukadinović D, Maziak W, Katmeh L, Schwarz V, Mahfoud F, Laufs U, Böhm M. Cardiovascular effects of waterpipe smoking: a systematic review and meta-analysis. Rev Cardiovasc Med. 2020;21:453–468. doi: 10.31083/j.rcm.2020.03.135. PubMed DOI
Jukema JB, Bagnasco DE, Jukema RA. Waterpipe smoking: not necessarily less hazardous than cigarette smoking: Possible consequences for (cardiovascular) disease. Neth Heart J. 2014;22:91–99. doi: 10.1007/s12471-013-0501-0. PubMed DOI PMC
Félétou M. Integrated Systems Physiology: from Molecule to Function to Disease. San Rafael (CA): Morgan & Claypool Life Sciences Copyright © 2011 by Morgan & Claypool Life Sciences Publishers; 2011. The Endothelium: Part 1: Multiple Functions of the Endothelial Cells-Focus on Endothelium-Derived Vasoactive Mediators. PubMed DOI
Rammah M, Dandachi F, Salman R, Shihadeh A, El-Sabban M. In vitro effects of waterpipe smoke condensate on endothelial cell function: a potential risk factor for vascular disease. Toxicol Lett. 2013;219:133–142. doi: 10.1016/j.toxlet.2013.02.015. PubMed DOI PMC
Nemmar A, Al-Salam S, Yuvaraju P, Beegam S, Yasin J, Ali BH. Chronic exposure to water-pipe smoke induces cardiovascular dysfunction in mice. Am J Physiol Heart Circ Physiol. 2017;312:H329–H339. doi: 10.1152/ajpheart.00450.2016. PubMed DOI
Nemmar A, Beegam S, Zaaba NE, Elzaki O, Pathan A, Ali BH. Waterpipe smoke inhalation induces lung injury and aortic endothelial dysfunction in mice. Physiol Res. 2023;72:337–347. doi: 10.33549/physiolres.935042. PubMed DOI PMC
Hamadi N, Beegam S, Zaaba NE, Elzaki O, Ali BH, Nemmar A. Comparative Study on the Chronic Vascular Responses Induced by Regular Versus Occasional Waterpipe Smoke Inhalation in Mice. Cell Physiol Biochem. 2022;56:13–27. doi: 10.33594/000000491. PubMed DOI
Bodas M, Van Westphal C, Carpenter-Thompson R, DKM, Vij N. Nicotine exposure induces bronchial epithelial cell apoptosis and senescence via ROS mediated autophagy-impairment. Free Radic Biol Med. 2016;97:441–453. doi: 10.1016/j.freeradbiomed.2016.06.017. PubMed DOI
Benedikter BJ, Volgers C, van Eijck PH, Wouters EFM, Savelkoul PHM, Reynaert NL, Haenen G, et al. Cigarette smoke extract induced exosome release is mediated by depletion of exofacial thiols and can be inhibited by thiol-antioxidants. Free Radic Biol Med. 2017;108:334–344. doi: 10.1016/j.freeradbiomed.2017.03.026. PubMed DOI
Al-Azawi A, Sulaiman S, Arafat K, Yasin J, Nemmar A, Attoub S. Impact of Sodium Dichloroacetate Alone and in Combination Therapies on Lung Tumor Growth and Metastasis. Int J Mol Sci. 2021;22:12553. doi: 10.3390/ijms222212553. PubMed DOI PMC
Allen M, Millett P, Dawes E, Rushton N. Lactate dehydrogenase activity as a rapid and sensitive test for the quantification of cell numbers in vitro. Clin Mater. 1994;16:189–194. doi: 10.1016/0267-6605(94)90116-3. PubMed DOI
Ali BH, Al Moundhri M, Eldin MT, Nemmar A, Al Siyabi S, Annamalai K. Amelioration of cisplatin-induced nephrotoxicity in rats by tetramethylpyrazine, a major constituent of the Chinese herb Ligusticum wallichi. Exp Biol Med (Maywood) 2008;233:891–896. doi: 10.3181/0711-RM-315. PubMed DOI
Higashi Y. Roles of Oxidative Stress and Inflammation in Vascular Endothelial Dysfunction-Related Disease. Antioxidants (Basel) 2022;11:1958. doi: 10.3390/antiox11101958. PubMed DOI PMC
D’Onofrio N, Prattichizzo F, Martino E, Anastasio C, Mele L, La Grotta R, Sardu C, et al. MiR-27b attenuates mitochondrial oxidative stress and inflammation in endothelial cells. Redox Biol. 2023;62:102681. doi: 10.1016/j.redox.2023.102681. PubMed DOI PMC
Nemmar A, Al-Salam S, Beegam S, Yuvaraju P, Ali BH. Aortic Oxidative Stress, Inflammation and DNA Damage Following Pulmonary Exposure to Cerium Oxide Nanoparticles in a Rat Model of Vascular Injury. Biomolecules. 2019;9:376. doi: 10.3390/biom9080376. PubMed DOI PMC
Miller MR, Newby DE. Air pollution and cardiovascular disease: car sick. Cardiovasc Res. 2020;116:279–294. doi: 10.1093/cvr/cvz228. PubMed DOI
Nemmar A, Hoylaerts MF, Nemery B. Effects of particulate air pollution on hemostasis. Clin Occup Environ Med. 2006;5:865–881. PubMed
Nemmar A, Al-Salam S, Beegam S, Zaaba NE, Elzaki O, Ali BH. Waterpipe smoke inhalation potentiates cardiac oxidative stress, inflammation, mitochondrial dysfunction, apoptosis and autophagy in experimental hypertension. Biomed Pharmacother. 2023;158:114144. doi: 10.1016/j.biopha.2022.114144. PubMed DOI
Aykul S, Martinez-Hackert E. Determination of half-maximal inhibitory concentration using biosensor-based protein interaction analysis. Anal Biochem. 2016;508:97–103. doi: 10.1016/j.ab.2016.06.025. PubMed DOI PMC
Kopel E, Kivity S, Morag-Koren N, Segev S, Sidi Y. Relation of serum lactate dehydrogenase to coronary artery disease. Am J Cardiol. 2012;110:1717–1722. doi: 10.1016/j.amjcard.2012.08.005. PubMed DOI
Zaaba NE, Al-Salam S, Beegam S, Elzaki O, Yasin J, Nemmar A. Catalpol Attenuates Oxidative Stress and Inflammation via Mechanisms Involving Sirtuin-1 Activation and NF-κB Inhibition in Experimentally-Induced Chronic Kidney Disease. Nutrients. 2023;15:237. doi: 10.3390/nu15010237. PubMed DOI PMC
Nemmar A, Al Salam S, Zia S, Dhanasekaran S, Shudadevi M, Ali BH. Time-course effects of systemically administered diesel exhaust particles in rats. Toxicol Lett. 2010;194:58–65. doi: 10.1016/j.toxlet.2010.02.001. PubMed DOI
Nemmar A, Al-Salam S, Yuvaraju P, Beegam S, Ali BH. Emodin mitigates diesel exhaust particles-induced increase in airway resistance, inflammation and oxidative stress in mice. Respir Physiol Neurobiol. 2015;215:51–57. doi: 10.1016/j.resp.2015.05.006. PubMed DOI
Al Suleimani YM, Ali BH, Ali H, Manoj P, Almashaiki KS, Abdelrahman AM. The Salutary Effects of Diminazene, Lisinopril or Valsartan on Cisplatin - Induced Acute Kidney Injury in Rats: A Comparative Study. Physiol Res. 2024;73:227–237. doi: 10.33549/physiolres.935210. PubMed DOI PMC
Yoshida M, Minagawa S, Araya J, Sakamoto T, Hara H, Tsubouchi K, Hosaka Y, et al. Involvement of cigarette smoke-induced epithelial cell ferroptosis in COPD pathogenesis. Nat Commun. 2019;10:3145. doi: 10.1038/s41467-019-10991-7. PubMed DOI PMC
Slíva J, Charalambous C, Bultas J, Karetová D. A new strategy for the treatment of atherothrombosis - inhibition of inflammation. Physiol Res. 2019;68(Suppl 1):S17–S30. doi: 10.33549/physiolres.934327. PubMed DOI
Rahman A, Kefer J, Bando M, Niles WD, Malik AB. E-selectin expression in human endothelial cells by TNF-alpha-induced oxidant generation and NF-kappaB activation. Am J Physiol. 1998;275:L533–L544. doi: 10.1152/ajplung.1998.275.3.L533. PubMed DOI
Yang Z, Knight CA, Mamerow MM, Vickers K, Penn A, Postlethwait EM, Ballinger SW. Prenatal environmental tobacco smoke exposure promotes adult atherogenesis and mitochondrial damage in apolipoprotein E−/− mice fed a chow diet. Circulation. 2004;110:3715–3720. doi: 10.1161/01.CIR.0000149747.82157.01. PubMed DOI
Fetterman JL, Sammy MJ, Ballinger SW. Mitochondrial toxicity of tobacco smoke and air pollution. Toxicology. 2017;391:18–33. doi: 10.1016/j.tox.2017.08.002. PubMed DOI PMC
Zorova LD, Popkov VA, Plotnikov EY, Silachev DN, Pevzner IB, Jankauskas SS, Babenko VA, et al. Mitochondrial membrane potential. Anal Biochem. 2018;552:50–59. doi: 10.1016/j.ab.2017.07.009. PubMed DOI PMC
Kuchařová M, Hronek M, Rybáková K, Zadák Z, Štětina R, Josková V, Patková A. Comet assay and its use for evaluating oxidative DNA damage in some pathological states. Physiol Res. 2019;68:1–15. doi: 10.33549/physiolres.933901. PubMed DOI
Omari Shekaftik S, Nasirzadeh N. 8-Hydroxy-2′-deoxyguanosine (8-OHdG) as a biomarker of oxidative DNA damage induced by occupational exposure to nanomaterials: a systematic review. Nanotoxicology. 2021;15:850–864. doi: 10.1080/17435390.2021.1936254. PubMed DOI
Pourahmad J, Aghvami M, Zarei MH, Naserzadeh P. Cigarette Smoke and Mitochondrial Damage. In: WILL E, DYKENS JE, editors. Mitochondrial Dysfunction Caused by Drugs and Environmental Toxicants. Wiley Online Library; 2018. pp. 709–725. DOI
Brentnall M, Rodriguez-Menocal L, De Guevara RL, Cepero E, Boise LH. Caspase-9, caspase-3 and caspase-7 have distinct roles during intrinsic apoptosis. BMC Cell Biol. 2013;14:32. doi: 10.1186/1471-2121-14-32. PubMed DOI PMC
Savitskaya MA, Onishchenko GE. Mechanisms of apoptosis. Biochemistry (Moscow) 2015;80:1393–1405. doi: 10.1134/S0006297915110012. PubMed DOI
Fitzgerald M-C, O’Halloran PJ, Connolly NMC, Murphy BM. Targeting the apoptosis pathway to treat tumours of the paediatric nervous system. Cell Death Dis. 2022;13:460. doi: 10.1038/s41419-022-04900-y. PubMed DOI PMC
Wang J, Wilcken DE, Wang XL. Cigarette smoke activates caspase-3 to induce apoptosis of human umbilical venous endothelial cells. Mol Genet Metab. 2001;72:82–88. doi: 10.1006/mgme.2000.3115. PubMed DOI
Messner B, Frotschnig S, Steinacher-Nigisch A, Winter B, Eichmair E, Gebetsberger J, Schwaiger S, et al. Apoptosis and necrosis: two different outcomes of cigarette smoke condensate-induced endothelial cell death. Cell Death Dis. 2012;3:e424. doi: 10.1038/cddis.2012.162. PubMed DOI PMC
Zhang C, Qin S, Qin L, Liu L, Sun W, Li X, Li N, Wu R, Wang X. Cigarette smoke extract-induced p120-mediated NF-κB activation in human epithelial cells is dependent on the RhoA/ROCK pathway. Sci Rep. 2016;6:23131. doi: 10.1038/srep23131. PubMed DOI PMC
Daijo H, Hoshino Y, Kai S, Suzuki K, Nishi K, Matsuo Y, Harada H, Hirota K. Cigarette smoke reversibly activates hypoxia-inducible factor 1 in a reactive oxygen species-dependent manner. Sci Rep. 2016;6:34424. doi: 10.1038/srep34424. PubMed DOI PMC
Fitzpatrick SF, Tambuwala MM, Bruning U, Schaible B, Scholz CC, Byrne A, O’Connor A, et al. An intact canonical NF-κB pathway is required for inflammatory gene expression in response to hypoxia. J Immunol. 2011;186:1091–1096. doi: 10.4049/jimmunol.1002256. PubMed DOI