ABSTRACT
Long-term exposure to microgravity and space radiation leads to physiological and pathological changes in human biology. Pathological neuro-ocular changes are collected under the name spaceflight-associated neuro-ocular syndrome. This review examines studies on the effects of microgravity and space radiation on the ocular structures and their results. In addition, we discuss treatment methods and hypotheses to reduce the effects of microgravity and space radiation on biological structures.
Keywords:
Space radiation, microgravity, spaceflight-associated neuro-ocular syndrome, artificial gravity
Introduction
The space race began on October 4, 1957, when the Soviet Union (USSR) launched the artificial satellite Sputnik 1, followed soon after by the first animal and manned flights. At present, space studies continue on the International Space Station (ISS), which was built by joining modules brought together in a collaborative project by the United States National Aerospace Agency (NASA), Russian Federal Space Agency (Roscosmos), European Space Agency (ESA), Canadian Space Agency (CAS-ASC), and Japan Aerospace Exploration Agency (JAXA). The ISS is an artificial satellite in low Earth orbit that can be inhabited by humans. Thanks to the ISS, the number of long-duration spaceflights such as low orbit flights and Moon missions is increasing. This has also increased the number of people exposed to space conditions. Space studies have revealed several problems that affect human biology, such as low gravity, lack of atmosphere, galactic cosmic rays (GCR), and solar energetic particles (SEP).1 Microgravity (MG) and space radiation constitute a major part of these problems. Solutions to these and many other problems are necessary to enable human beings to explore the solar system and beyond.
GCR and SEP are an important problem affecting manned space missions. GCR consist of high-energy protons, high-energy ions, neutrons, gamma and x-rays, and secondary particles formed as a result of particles colliding with spacecraft and human tissues. These rays cause molecular bond breaks and mutations in DNA, resulting in cell damage, tumors and tissue degeneration, cataract, heart disease, central nervous system damage, and acute radiation syndrome.2 The effects of radiation on human tissues can be investigated by examining dosimetric results in people with occupational radiation exposure on Earth and those participating in space missions, as well as radiation dose information obtained from robotic exploration tools sent to planets for research purposes. However, all of these are indirect assessments. It should be noted that the detectors are silicone in structure. The annual radiation dose limit for people with occupational radiation exposure on Earth is 50 millisievert (mSv).3 Although the ISS is slightly protected by Earth’s magnetic field, the level of radiation exposure for humans in the station was measured as approximately 200 mSv per year.4 According to data obtained by the radiation assessment detector on the Curiosity space probe sent to Mars, the approximate dose of radiation exposure incurred during the roundtrip flight to Mars (2x180 days) and 500 days on the Mars surface was calculated as 1.01 Sv.5 Radiation exposure on the surface of Mars is greater than on Earth because Mars has a thin atmosphere and no global magnetic field to deflect energy-laden particles. According to results obtained in the Chinese Chang’e 4 robotic mission to the Moon’s Von Kármán crater, the daily GCR dose on the Moon’s surface was found to be 2.6 times higher than the daily exposure on the ISS.6 Epidemiological data indicate that exposure to 1 Sv of radiation increases the likelihood of cancer development by 5.5%.4 In this case, long-duration deep space missions are many times over the current physiological limits. Therefore, solutions must be developed to protect crew members from space radiation.
Table 1 shows the upper limits for space radiation exposure of tissues and organs determined by the International Commission on Radiological Protection.7
Conclusion
Further research is needed to increase human resilience to the conditions of space. Attempting to improve our understanding of the physiopathology of SANS and the effect of radiation on tissues will not only help people traveling in space, but also elucidate the physiopathology of diseases seen on Earth. The mechanisms of optic nerve supply and CSF circulation around the optic nerve are still unclear. The MG environment has demonstrated what can happen when fluid dynamics are altered. These studies will enable us to better understand the fluid and tissue dynamics of the optic nerve and develop novel approaches to optic nerve diseases.
References
1Alexander DJ, Gibson RC, Hamilton DR, Lee SMC, Mader TH, Otto C, Oubre CM, Pass AF, Platts SH, Scott JM, Smith SM, Stenger MB, Westby CM, Zanello SB. Human Research Program Human Health Countermeasures Element Evidence Report Risk of Spaceflight-Induced Intracranial Hypertension and Vision Alterations. 2012.
2Cucinotta FA, Kim M-HY, Ren L. Evaluating shielding effectiveness for reducing space radiation cancer risks. Radiation Measurements. 2006;41:1173-1185.
3ICRP. The 2007 Recommendations of the International Commission on Radiological Protection. ICRP Publication 103. Ann. ICRP 37 (2-4).
4Zeitlin C, Hassler DM, Cucinotta FA, Ehresmann B, Wimmer-Schweingruber RF, Brinza DE, Kang S, Weigle G, Böttcher S, Böhm E, Burmeister S, Guo J, Köhler J, Martin C, Posner A, Rafkin S, Reitz G. Measurements of energetic particle radiation in transit to Mars on the Mars Science Laboratory. Science. 2013;340:1080-1084.
5Hassler DM, Zeitlin C, Wimmer-Schweingruber RF, Ehresmann B, Rafkin S, Eigenbrode JL, Brinza DE, Weigle G, Böttcher S, Böhm E, Burmeister S, Guo J, Köhler J, Martin C, Reitz G, Cucinotta FA, Kim MH, Grinspoon D, Bullock MA, Posner A, Gómez-Elvira J, Vasavada A, Grotzinger JP. Mars’ surface radiation environment measured with the Mars Science Laboratory’s Curiosity rover. Science. 2014;343:1244797.
6Zhang S, Wimmer-Schweingruber RF, Yu J, Wang C, Fu Q, Zou Y, Sun Y, Wang C,, Hou D, S. B. I., Burmeister S, Seimetz L, Schuster B, Knierim V, Shen G, Yuan B, Lohf H,, Guo J, X. Z., Freiherr von Forstner JL, Kulkarni SR, Xu H, Xue C, Li J, Zhang Z, Zhang H, & Berger T, M. D., Hellweg CE, Hou X, Cao J, Chang Z, Zhang B, Chen Y, Geng H, Quan Z. First measurements of the radiation dose on the lunar surface. Sci. Adv. 2020;6:eaaz1334.
7Cucinotta FA. NASA’s Permisible Exposure Limits, NASA Space Flight Human-System Standard Radiation risk acceptability and limitations. Washington D.C2010: 5-6.
8Charman WN, Dennis JA, Fazio GG, Jelley JV. Visual sensations produced by single fast particles. Nature. 1971;230:522-524.
9Duntley SQ, Austin RW, Taylor JH, Harris JH. Experiment S-8/D-13, Visual Acuity and Astronaut Visibility. 1966;121:329.
10Narici L, Bidoli V, Casolino M, De Pascale MP, Furano G, Morselli A, Picozza P, Reali E, Sparvoli R, Licoccia S, Romagnoli P, Traversa E, Sannita WG, Loizzo A, Galper A, Khodarovich A, Korotkov MG, Popov A, Vavilov N, Avdeev S, Salnitskii VP, Shevchenko OI, Petrov VP, Trukhanov KA, Boezio M, Bonvicini W, Vacchi A, Zampa N, Battiston R, Mazzenga G, Ricci M, Spillantini P, Castellini G, Carlson P, Fuglesang C. ALTEA: anomalous long term effects in astronauts. A probe on the influence of cosmic radiation and microgravity on the central nervous system during long flights. Adv Space Res. 2003;31:141-146.
11Mathis T, Vignot S, Leal C, Caujolle JP, Maschi C, Mauget-Faÿsse M, Kodjikian L, Baillif S, Herault J, Thariat J. Mechanisms of phosphenes in irradiated patients. Oncotarget. 2017;8:64579-64590.
12Newman F, Asadi-Zeydabadi M, Durairaj VD, Ding M, Stuhr K, Kavanagh B. Visual sensations during megavoltage radiotherapy to the orbit attributable to Cherenkov radiation. Med Phys. 2008;35:77-80.
13Fuglesang C, Narici L, Picozza P, Sannita WG. Phosphenes in low earth orbit: survey responses from 59 astronauts. Aviat Space Environ Med. 2006;77:449-452.
14Avdeev S, Bidoli V, Casolino M, De Grandis E, Furano G, Morselli A, Narici L, De Pascale MP, Picozza P, Reali E, Sparvoli R, Boezio M, Carlson P, Bonvicini W, Vacchi A, Zampa N, Castellini G, Fuglesang C, Galper A, Khodarovich A, Ozerov Y, Popov A, Vavilov N, Mazzenga G, Ricci M, Sannita WG, Spillantini P. Eye light flashes on the Mir space station. Acta Astronaut. 2002; 50:511-525.
15Narici L, De Martino A, Brunetti V, Rinaldi A, Sannita W, Paci MJRM. Radicals excess in the retina: a model for light flashes in space. 2009;44:203-205.
16Lipman RM, Tripathi BJ, Tripathi RC. Cataracts induced by microwave and ionizing radiation 1988;33:200-210.
17Belkacémi Y, Touboul E, Méric J.B. Rat P, Warnet JM. Cataracte radio-induite: aspects physiopathologiques,radiobiologiques et cliniques.Cancer/Radiother 2001;5:397-412.
18Chylack LT , Feiveson AH, Peterson LE, Tung WH, Wear ML, Marak LJ, Hardy DS, Chappell LJ, Cucinotta FA. NASCA report 2: Longitudinal study of relationship of exposure to space radiation and risk of lens opacity. Radiat Res. 2012;178:25-32.
19Little MP, Cahoon EK, Kitahara CM,Simon SL, Hamada N.Linet MS. Occupational radiation exposure and excess additive risk of cataract incidence in a cohort of US radiologic technologists. Occup Environ Med. 2020;77:1-8.
20Pandiarajan M, Hargens AR. Ground-Based Analogs for Human Spaceflight. Front Physiol.2020;11:716.
21Gharib C, Hughson RL. Fluid and electrolyte regulation in space. Adv Space Biol Med.1992;2:113-130.
22Huang AS, Stenger MB, Macias BR. Gravitational Influence on Intraocular Pressure: Implications for Spaceflight and Disease. J Glaucoma. 2019;28:756-764.
23Aleci C. From international ophthalmology to space ophthalmology: the threats to vision on the way to Moon and Mars colonization. Int Ophthalmol. 2020;40:775-786.
24Pietrzyk RA, Jones JA, Sams CF, Whitson PA. Renal stone formation among astronauts. Aviat Space Environ Med. 2007;78:A9-13.
25Mader TH, Gibson CR, Pass AF, Kramer LA, Lee AG, Fogarty J, Tarver WJ, Dervay JP, Hamilton DR, Sargsyan A, Phillips JL, Tran D, Lipsky W, Choi J, Stern C, Kuyumjian R, Polk JD. Optic disc edema, globe flattening, choroidal folds, and hyperopic shifts observed in astronauts after long-duration space flight. Ophthalmology. 2011;118:2058-2069.
26Mader TH, Gibson CR, Hart SF, Lee AG. Asymmetric Papilledema in Idiopathic Intracranial Hypertension: Comment. J Neuroophthalmol. 2016;36:111-112.
27Mader TH, Gibson CR, Otto CA, Sargsyan AE, Miller NR, Subramanian PS, Hart SF, Lipsky W, Patel NB, Lee AG. Persistent Asymmetric Optic Disc Swelling After Long-Duration Space Flight: Implications for Pathogenesis. J Neuroophthalmol. 2017;37:133-139.
28Dailey RA, Mills RP, Stimac GK, Shults WT, Kalina RE. The natural history and CT appearance of acquired hyperopia with choroidal folds. Ophthalmology. 1986;93:1336-1342.
29Sibony PA, Kupersmith MJ, Feldon SE, Wang JK, Garvin M. Retinal and Choroidal Folds in Papilledema. Invest Ophthalmol Vis Sci. 2015;56:5670-5680.
30Newell FW. Choroidal folds. The seventh Harry Searls Gradle Memorial lecture. Am J Ophthalmol. 1973;75:930-942.
31Chiquet C, Custaud MA, Le Traon AP, Millet C, Gharib C, Denis P. Changes in intraocular pressure during prolonged (7-day) head-down tilt bedrest. J Glaucoma. 2003;12:204-208.
32Draeger J, Schwartz R, Groenhoff S, Stern C. Self-tonometry under microgravity conditions. Clin Investig. 1993;71:700-703.
33Mader TH, Gibson CR, Caputo M, Hunter N, Taylor G, Charles J, Meehan RT. Intraocular pressure and retinal vascular changes during transient exposure to microgravity. Am J Ophthalmol. 1993;115:347-350.
34Mader TH, Taylor GR, Hunter N, Caputo M, Meehan RT. Intraocular pressure, retinal vascular, and visual acuity changes during 48 hours of 10 degrees head-down tilt. Aviat Space Environ Med. 1990;61:810-813.
35Friberg TR, Sanborn G, Weinreb RN. Intraocular and episcleral venous pressure increase during inverted posture. Am J Ophthalmol. 1987;103:523-526.
36Shinojima A, Iwasaki K, Aoki K, Ogawa Y, Yanagida R, Yuzawa M. Subfoveal choroidal thickness and foveal retinal thickness during head-down tilt. Aviat Space Environ Med. 2012; 83:388-393.
37Manko OM, Smoleevsky AE, Tomilovskaya ES, Kozlovskaya IB. Effect of 5-day dry immersion on eye hydrodynamics. Aviakosmicheskaya i Ekologicheskaya Meditsina (Russia). 2019;V.53,π5,22-28.
38Marshall-Goebel K, Stevens B, Rao CV, Suarez JI, Calvillo E, Arbeille P, Sangi-Haghpeykar H, Donoviel DB, Mulder E, Bershad EM. Internal Jugular Vein Volume During Head-Down Tilt and Carbon Dioxide Exposure in the SPACECOT Study. Aerosp Med Hum Perform. 2018;89:351-356.
39Karina Marshall-Goebel K, Laurie SS, Alferova IV. Assessment of Jugular Venous Blood Flow Stasis and Thrombosis During Spaceflight. JAMA Netw Open. 2019;2:e1915011.
40Förstermann U. Nitric oxide and oxidative stress in vascular disease. Pflugers Arch. 2010;459:923-939.
41Zwart SR, Gibson CR, Mader TH, Ericson K, Ploutz-Snyder R, Heer M, Smith SM. Vision changes after spaceflight are related to alterations in folate- and vitamin B-12-dependent one-carbon metabolism. J Nutr. 2012;142:427-431.
42Giuseffi V, Wall M, Siegel PZ, Rojas PB. Symptoms and disease associations in idiopathic intracranial hypertension (pseudotumor cerebri): a case-control study. Neurology.1991;41:239-244.
43Bidot S, Bruce BB, Saindane AM, Newman NJ, Biousse V. Asymmetric papilledema in idiopathic intracranial hypertension. J Neuroophthalmol. 2015;35:31-36.
44Mader TH, Gibson CR, Pass AF, Lee AG, Killer HE, Hansen HC, Dervay JP, Barratt MR, Tarver WJ, Sargsyan AE, Kramer LA, Riascos R, Bedi DG, Pettit DR. Optic disc edema in an astronaut after repeat long-duration space flight. J Neuroophthalmol. 2013;33:249-255.
45Killer HE, Jaggi GP, 2 Flammer J, Miller NR, Huber AR, Mironov A. Cerebrospinal fluid dynamics between the intracranial and the subarachnoid space of the optic nerve. Is it always bidirectional? Brain. 2007;130:514-520.
46Mesa-Gutiérrez JC, Quiñones SM, Ginebreda JA. Optic nerve sheath meningocele. Clin Ophthalmol. 2008;2:661-668.
47Bakbak B, Dönmez H, Kansu T, Kiratli H. Dural ectasia of the optic nerve sheath: is it always benign? Eye Brain. 2009;1:5-7.
48Mathieu E, Gupta N, Ahari A, Zhou X, Hanna J, Yücel YH. Evidence for Cerebrospinal Fluid Entry Into the Optic Nerve via a Glymphatic Pathway. Invest Ophthalmol Vis Sci. 2017;58:4784-4791.
49Wostyn P, Killer HE, De Deyn PP. Glymphatic stasis at the site of the lamina cribrosa as a potential mechanism underlying open-angle glaucoma. Clin Exp Ophthalmol. 2017;45:539-547.
50Thornton W, Bonato F. Cephalic Fluid Dynamics and Ocular Changes in Weightlessness. The Human Body and Weightlessness; Springer. 2017:99-120.
51Hargens AR, Bhattacharya R, Schneider SM. Space physiology VI: exercise, artificial gravity, and countermeasure development for prolonged space flight. Eur J Appl Physiol. 2013;113:2183-2192.
52Clément G. International roadmap for artificial gravity research. NPJ Microgravity. 2017;3:29.
53Gruber K, Seyedmadani K, Torin C. The Turbolift: Linear Sled Hybrid Artificial Gravity Concept 2018 NASA Innovative Advance Concepts (NIAC) Phase I Final Report NNX17AJ77G.
54Macias BR, Liu JH, Grande-Gutierrez N, Hargens AR. Intraocular and intracranial pressures during head-down tilt with lower body negative pressure. Aerosp Med Hum Perform. 2015;86:3-7.
55Lee SMC, Ribeiro LC, Laurie SS, Feiveson AH, Kitov VV, Kofman IS, Macias BR, Rosenberg M, Rukavishnikov IV, Tomilovskaya ES, Bloomberg JJ, Kozlovskaya IB, Reschke MF, Stenger MB Efficacy of Gradient Compression Garments in the Hours After Long-Duration Spaceflight. Front. Physiol. 2020;11:784.
56Taibbi G, Cromwell RL, Kapoor KG, Godley BF, Vizzeri G. The effect of microgravity on ocular structures and visual function: a review. Surv Ophthalmol. 2013;58:155-163.
57Özdemir T, Akbay I, Uzun H, Reyhancan IA. Neutron shielding of EPDM rubber with boric acid: mechanical, thermal properties and neutron absorption tests. Progress in Nuclear Energy. 2016;89:102-109.
58Ruhlmann S. The FLARE Suit: A protection against solar radiation in space.Degree project in mechanical engineering, second cycle, 30 credits, Stockholm, Sweden 2019.
59Baiocco G, Giraudo M, Bocchini L, Barbieri S, Locantore I, Brussolo E, Giacosa D, Meucci L, Steffenino S, Ballario A, Barresi B, Barresi R, Benassai M, Ravagnolo L, Narici L, Rizzo A, Carrubba E, Carubia F, Neri G, Crisconio M, Piccirillo S, Valentini G, Barbero S, Giacci M, Lobascio C, Ottolenghi A. A water-filled garment to protect astronauts during interplanetary missions tested on board the ISS. Life Sci Space Res (Amst). 2018;18:1-11.
60Kennedy AR, Weissman D, Sanzari JK, Krigsfeld GS, Wan XS, Romero-Weaver AL, Diffenderfer ES, Lin L, Cengel K. Acute effects of solar particle event radiation. J Radiat Res. 2014;55:i66-i67.
61Langell J, Jennings R, Clark J, Ward JB. Pharmacological agents for the prevention and treatment of toxic radiation exposure in spaceflight. Aviat Space Environ Med. 2008;79:651-660.
62Wambi C, Sanzari J, Wan XS, Nuth M, Davis J, Ko YH, Sayers CM, Baran M, Ware JH, Kennedy AR. Dietary antioxidants protect hematopoietic cells and improve animal survival after total-body irradiation.Radiat Res. 2008;169:384-396.