Hyperbaric Oxygen Attenuates Aortic Vasoconstriction after Simulated Microgravity in Rats

Crossmark: check for updates

Authors

  • Judy R. Wilson Department of Kinesiology,The University of Texas at Arlington, College of Nursing and Health Innovation, P. O. Box 19259, Arlington,TX 76019, USA
  • Jeremiah Campbell Department of Kinesiology,The University of Texas at Arlington, College of Nursing and Health Innovation, P. O. Box 19259, Arlington,TX 76019, USA

DOI:

https://doi.org/10.17140/SEMOJ-7-183

Keywords:

Hyperbaric oxygen, Vascular reactivity, Hindlimb suspension

Abstract

Background
The hindlimb suspended (HLS) rat model has been used in land-based research to evaluate effects of simulated microgravity. Previous research demonstrated that 2-4 weeks of HLS reduced vasoconstrictive responses of aortic, mesenteric, and femoral arterial rings to phenylephrine (PHE) while acute exposure to hyperoxia amplified constrictive responses to PHE. The purpose of this study was to determine if hyperbaric oxygen treatment (HBO) during HLS would reverse the attenuation of the vasoconstrictive response.
Methods
Five-month-old male Sprague Dawley rats were randomly divided into aging controls (AC), AC-HBO, HLS, and HLS-HBO. Groups receiving HBO (AC-HBO; HLS-HBO) were placed in a cage that was fitted for the animal hyperbaric chamber to maintain HLS. HBO groups received 24 treatments, once a day, 6 d/week using a wound care protocol. The chamber was flushed with 100% oxygen, compressed over 10 min to 2.5 atmospheres absolute (ATA) (22.5 psig), a 90-minute treatment, then a 10 min decompression. After 28 d of HLS, animals were sacrificed under isoflurane anesthesia and thoracic aorta segments isolated. Relaxation of aortic rings was measured in response to acetylcholine (ACh) and sodium nitroprusside (SNP) after pre-constriction with PHE (3×10-7). Constriction of aortic rings was also determined in response to increasing concentrations of PHE. All drugs were administered cumulatively in vessel baths at 10-10-10-4 M. Data were analyzed using four-parameter (i.e., minimum, maximum, EC50, slope) nonlinear regression, and groups compared using 2×2 ANOVA with HBO and HLS as main effects.
Results
Responses to ACh and SNP were not affected by HLS or HBO. However, in response to PHE, there was a decrease in maximum vasoconstriction in HLS compared to controls (44.7±7.3% vs 82.4±6.0%, respectively, p≤0.05) and in HBO compared to controls (48.5±6.5% vs 78.6±6.8%, p≤0.05).
Conclusion
These results indicate that PHE-induced constriction of thoracic aorta is decreased after HLS. HBO did not reverse HLS-induced reductions in contractile responses; instead, HBO independently reduced PHE-stimulated constriction of aortic segments. This suggests that HBO may be useful in conditions where constriction is enhanced, such as diabetes.

References

NASA Sciences. Mars 2020 Mission Perseverance Rover. Web site. mars.nasa.gov/mars. Accessed March 30, 2021.

Sibonga JD, Evans HJ, Sung HG, Spector ER, Lang TF, Oganov VS, et al. Recovery of spaceflight-induced bone loss: Bone mineral density after long-duration missions as fitted with an exponential function. Bone. 2007; 41(6): 973-978. doi: 10.1016/j. bone.2007.08.022

Blaber E, Marçal H, Burns BP. Bioastronautics: The influence of microgravity on astronaut health. Astrobiology. 2010; 10(5): 463-473. doi: 10.1089/ast.2009.0415

Ren XL, Zhang R, Zhang YY, Liu H, Yu J-W, Cai Y, et al. Nitric oxide synthase activity in the abdominal aorta of rats is decreased after 4 weeks of simulated microgravity. Clin Exp Pharmacol Physiol. 2011; 38(10): 683-687. doi: 10.1111/j.1440-1681.2011.05565.x

Fogleman G, Leveton L, Charles J. The bioastronautics ro dmap: A risk reduction strategy for human exploration. In: 1st Space Ex-ploration Conference: Continuing the Voyage of Discovery. Amer-ican Institute of Aeronautics and Astronautics; 2005.

Morey-Holton ER, Globus RK. Hindlimb unloading rodent model: technical aspects. J Appl Physiol (1985). 2002; 92(4): 1367- 1377. doi: 10.1152/japplphysiol.00969.2001

Regnard J, Heer M, Drummer C, Norsk P. Validity of micrograv-ity simulation models on earth. Am J Kidney Dis. 2001; 38(3): 668- 674. doi: 10.1053/ajkd.2001.27753

Cowings P, Toscano W, Kanis D, Saicheur T, Ravikumar A, Ge-Original Research | Volume 7 | Number 1 | Wilson JR et al breyesus F. Fluid loading effects on temporal profiles of cardiovas-cular responses to head-down tilt. Aerosp Med Hum Perform. 2015; 86(2): 88-96. doi: 10.3357/AMHP.4065.2015

Grenon SM, Hurwitz S, Sheynberg N, Xiao X, Ramsdell CD, Mai CL, et al. Role of individual predisposition in orthostatic intoler-ance before and after simulated microgravity. J Appl Physiol (1985). 2004; 96(5): 1714-1722. doi: 10.1152/japplphysiol.01274.2003

Shibata S, Perhonen M, Levine BD. Supine cycling plus volume loading prevent cardiovascular deconditioning during bed rest. J Appl Physiol (1985). 2010; 108(5): 1177-1186. doi: 10.1152/jap-plphysiol.01408.2009

Meck JV, Waters WW, Ziegler MG, deBlock HF, Mills PJ, Robertson D, et al. Mechanisms of postspaceflight orthostatic hypotension: Low alpha1-adrenergic receptor responses before flight and central autonomic dysregulation postflight. Am J Physiol Heart Circ Physiol. 2004; 286(4): H1486-H1495. doi: 10.1152/ajp-heart.00740.2003

Mulvagh SL, Charles JB, Riddle JM, Rehbein TL, Bungo MW. Echocardiographic evaluation of the cardiovascular effects of short-duration spaceflight. J Clin Pharmacol. 1991; 31(10): 1024- 1026. doi: 10.1002/j.1552-4604.1991.tb03666.x

Buckey JC, Jr., Lane LD, Levine BD, Watenpaugh DE, Wright SJ, Moore WE, et al. Orthostatic intolerance after spaceflight. J Appl Physiol (1985). 1996; 81(1): 7-18. doi: 10.1152/jappl.1996.81.1.7

Martel E, Champeroux P, Lacolley P, Richard S, Safar M, Cuche JL. Central hypervolemia in the conscious rat: A model of cardio-vascular deconditioning. J Appl Physiol (1985). 1996; 80(4): 1390- 1396. doi: 10.1152/jappl.1996.80.4.1390

Moffitt JA, Foley CM, Schadt JC, Laughlin MH, Hasser EM. Attenuated baroreflex control of sympathetic nerve activity after cardiovascular deconditioning in rats. Am J Physiol. 1998; 274(5 Pt 2): R1397-R1405. doi: 10.1152/ajpregu.1998.274.5.r1397

Weaver L, Howe S, Snow G, Deru K. Arterial and pulmonary arterial hemodynamics and oxygen delivery/extraction in normal humans exposed to hyperbaric air and oxygen. J Appl Physiol (1985). 2009; 107(1): 336-345. doi: 10.1152/japplphysiol.91012.2008

Kranke P, Bennett MH, Martyn-St James M, Schnabel A, Debus SE, Weibel S. Hyperbaric oxygen therapy for chronic wounds. Cochrane Database Syst Rev. 2015; 2015(6): Cd004123. doi: 10.1002/14651858.CD004123.pub2

Wolin MS, Ahmad M, Gupte SA. Oxidant and redox signaling in vascular oxygen sensing mechanisms: Basic concepts, current controversies, and potential importance of cytosolic NADPH. Am J Physiol Lung Cell Mol Physiol. 2005; 289(2): L159-L173. doi: 10.1152/ajplung.00060.2005

Pasgaard T, Stankevicius E, Jørgensen MM, Ostergaard L, Si-monsen U, Frøbert O. Hyperoxia reduces basal release of nitric oxide and contracts porcine coronary arteries. Acta physiol (Oxf). 2007; 191(4): 285-296. doi: 10.1111/j.1748-1716.2007.01745.x

Dallinger S, Dorner GT, Wenzel R, Graselli U, Findl O, Eichler HG, et al. Endothelin-1 contributes to hyperoxia-induced vasocon-striction in the human retina. Invest Ophthalmol Vis Sci. 2000; 41(3): 864-869.

Dragic S, Momcicevic D, Zlojutro B, Jandric M, Kovacevic T, Djajić V, et al. Serum levels of nitric oxide and endothelin-1 in vas-culopathy managed with hyperbaric oxygen therapy. Clin Hemorheol Microcirc. 2020; 75(2): 233-241. doi: 10.3233/CH-190796

Drenjancevic I, Kibel A. Restoring vascular function with hy-perbaric oxygen treatment: Recovery mechanisms. J Vasc Res. 2014; 51(1): 1-13. doi: 10.1159/000355925

Li Y, Hao YF, Wang T, Zhang L-F, Liang Y, Xiao W-L, et al. Hyperbaric oxygen may improve vascular endothelial function in patients undergoing coronary stent implantation. Undersea Hyperb Med. 2019; 46(2): 145-152.

Kudchodkar BJ, Wilson J, Lacko A, Dory L. Hyperbaric oxygen reduces the progression and accelerates the regression of athero-sclerosis in rabbits. Arterioscler Thromb Vasc Biol. 2000; 20(6): 1637- Submit your article to this journal | https://openventio.org/submit-manuscript/ 1643. doi: 10.1161/01.atv.20.6.1637

Rowley WR, Bezold C, Arikan Y, Byrne E, Krohe S. Diabe-tes 2030: Insights from yesterday, today, and Future Trends. Popul Health Manag. 2017; 20(1): 6-12. doi: 10.1089/pop.2015.0181

Zamboni WA, Roth AC, Russell RC, Graham B, Suchy H, Kucan JO. Morphologic analysis of the microcirculation during reperfusion of ischemic skeletal muscle and the effect of hy-perbaric oxygen. Plast Reconstr Surg. 1993; 91(6): 1110-1123. doi: 10.1097/00006534-199305000-00022

Marx RE, Ehler WJ, Tayapongsak P, Pierce LW. Relationship of oxygen dose to angiogenesis induction in irradiated tissue. Am J Surg. 1990; 160(5): 519-524. doi: 10.1016/s0002-9610(05)81019-0

Karadurmus N, Sahin M, Tasci C, Naharci I, Ozturk C, Ilbas-mis S, et al. Potential benefits of hyperbaric oxygen therapy on ath-erosclerosis and glycaemic control in patients with diabetic foot. Endokrynol Pol. 2010; 61(3): 275-279.

Resanović I, Zarić B, Radovanović J, Sudar-Milovanović E, Gluvić Z, Jevremović D, et al. Hyperbaric oxygen therapy and vas-cular complications in diabetes mellitus. Angiology. 2020; 71(10): 876-885. doi: 10.1177/0003319720936925

Published

2021-05-13

How to Cite

Judy R. Wilson, & Jeremiah Campbell. (2021). Hyperbaric Oxygen Attenuates Aortic Vasoconstriction after Simulated Microgravity in Rats. Sports and Exercise Medicine , 7(1), 6–11. https://doi.org/10.17140/SEMOJ-7-183

Most read articles by the same author(s)