Literature DB >> 27867478

Theoretical considerations on the ultimate depth that could be reached by saturation human divers.

Jacques H Abraini1, Hélène N David2, Nicolas Vallée3, Jean-Jacques Risso3.   

Abstract

The occurrence of paroxysmal narcotic episodes including psychotic-like symptoms in divers participating to experimental deep diving programs with various gas mixtures has constituted, beyond the classical symptoms of the high-pressure neurological syndrome, the major limitation for deep diving. With the development of new saturation deep diving programs and experiments by the eastern nations, such as India and China, we believed that it is of interest to examine what could be the ultimate depth that could be reached by saturation human divers. Based on previous data and the critical volume model of inert gas narcosis, we propose that the ultimate depth for saturation diving could be around 1,000 m.

Entities:  

Keywords:  deep diving; high-pressure neurological syndrome; inert gas narcosis; psychotic-like disorders; ultimate depth

Year:  2016        PMID: 27867478      PMCID: PMC5110125          DOI: 10.4103/2045-9912.184722

Source DB:  PubMed          Journal:  Med Gas Res        ISSN: 2045-9912


When divers are exposed to depth, i.e. to increased pressure (10 m = 1 atmosphere absolute (ATA); 1 ATA = 0.1 MPa), both the pressure and the partial pressure of each gas in the breathing mixture that dissolve within the divers’ body affect the divers’ organism. The development of saturation diving has removed the constraint of repetitive decompression, leading to a gain of decompression time. As well, the replacement in “air” of nitrogen by helium, which is the inert gas that possesses the lowest narcotic potency, has removed the constraint of nitrogen narcosis (Bennett, 1993). However, at a depth greater than 200 m (21 ATA), breathing helium-oxygen mixtures induces the high-pressure neurological syndrome (HPNS) that is considered to be a function of raised pressure per se and is exacerbated by fast compression rates. This syndrome manifests itself by a general hyperexcitability mainly characterized in man by tremor, myoclonus, electroencephalographic changes, and alterations in cognitive functions. At higher pressure, using faster compression rates than those used in human dives, convulsions occur in animals including primates at around 1,000 m (101 ATA) (Halsey, 1982; Bennett and Rostain, 1993). Strategies used to reduce HPNS mainly include slow compression rates with stages, adaptation with time at depth, and the addition to the basic helium-oxygen breathing mixtures of narcotic gases such as nitrogen and hydrogen. This has allowed human divers to reach depths up to 534.4 m (54.4 ATA) in the open sea as well as pressures up to 71.1 ATA corresponding to simulated depths of up to 701 m in hyperbaric chambers. However, despite such strategies, experimental deep dives using hydrogen-oxygen, helium-hydrogen-nitrogen-oxygen, and helium-nitrogen-oxygen breathing mixtures () have had to be stopped because some of the divers experienced psychotic-like disorders (Stoudemire et al., 1984; Douchet et al., 1990; Raoul et al., 1991). Also, interestingly, similar disorders have been reported in pioneer dives with air (Adolfson and Muren, 1965). These symptoms clearly constitute beyond the classical symptoms of HPNS the major limitation to deep diving whatever the gas mixtures used. Among the features shown by the divers were hallucinations, agitation, delirium, and paranoid thoughts. These critical events were demonstrated to be paroxysmal narcotic symptoms that resulted from the sum of the narcotic potency of each gas that composed the diving breathing mixtures (Abraini, 1995a, b). With the development of deep diving successful programs and experiments by eastern nations, such India and China, we believed that is of interest to examine what could be the ultimate depth that could be reached by saturation human divers. Environmental conditions of absolute pressure and partial pressure of each inert gas during the experimental dives in which paroxysmal narcotic episodes occurred Diving gases at raised pressure has narcotic effects which relative potencies are highly correlated with lipid solubility (Smith and Paton, 1976; Dodson et al., 1985; Bennett, 1993; Abraini, 1995a, b). Although their structural mechanisms of action-thought to be similar to that of the noble and general anesthetic gases xenon and nitrous oxide (Colloc’h et al., 2007; Abraini et al., 2014; Sauguet et al., 2016)-are still under discussion (Dodson et al., 1985; Abraini et al., 1998; David et al., 2001; Abraini et al., 2003), the critical volume model (or some extension of it) (Miller et al., 1973; Halsey et al., 1978; Abraini, 1995a, b) has allowed predictive studies in both humans (Abraini, 1995a, b, 1997) and experimental animals (Dodson et al., 1985). This model states that, for a similar pharmacological effect, narcosis occurs when the volume of a hydrophobic cell region is caused to expand beyond a certain critical volume by the absorption of an inert substance. The fractional expansion E that occurs when a gas at a partial pressure P dissolves in the hydrophobic site is given by: E = Vi . Xi . Pi/Vm Where V is the partial molar volume of the gas in the solvent (or some model of it such as olive oil or benzene) of molar volume V and X is the mole fraction solubility of the gas in that solvent when its partial pressure is 1 ATA. For a mixture of gases, the net effect is given by the sum of the individual terms if each gas. indicates the values for V and X for the range of gases that have been used for deep diving; the value of V is estimated to be 640 mL (Dodson et al., 1985). Partial molar volume and mole fraction solubility of the gases used during the experimental dives in which paroxysmal narcotic episodes occurred using benzene as a model of the gases’ hydrophobic site of action Given that the psychotic-like episodes occurring at raised pressure have been shown to result from the sum of the narcotic potency of each gas used to compose the breathing mixture, the advantage of adding the narcotic gases nitrogen or hydrogen to the basic helium-oxygen breathing mixture does not appear readily apparent inasmuch the physical strategies used to reduce HPNS, such as slow compression rates with stages and adaptation with time at depth, have allowed divers breathing helium-oxygen mixtures to reach depths up to 610 (62 ATA) as early as the 1970s (Bennett and Rostain, 1993). As shown in , calculations with the critical volume model have allowed establishing that the mean expansion of the diving gas hydrophobic site of action necessary for the expression of psychotic-like narcotic episodes is about 0.0453 ± 0.0032% (Abraini, 1995a, b). As also illustrated in , taking into account this expansion value, the onset depth for the occurrence of psychotic-like disorders with the basic helium-oxygen mixture may be estimated between 930 m and 1,080 m (94–109 ATA) (mean depth: 1,005 m, i.e., 101.5 ATA). Full squares represent the net theoretical expansion of the gases’ hydrophobic site of action, using benzene as a model solvent, at the time paroxysmal narcotic episodes occurred using air, and hydrogen (H2)-oxygen (O2), helium (He)-H2-nitrogen (N2)-O2, or H2-N2-O2 breathing mixtures. Note: Data show that whatever the gas mixture used the fractional expansion was remarkably similar (mean value: 0.0453 ± 0.0032%) at the time the dives have had to be stopped because of the occurrence of paroxysmal narcotic episodes including psychotic-like symptoms. Taking into account this expansion value, the onset depth for the occurrence of paroxysmal narcotic episodes in helium-oxygen mixture may be thus estimated between 930 m and 1,080 m (94–109 ATA). 1 ATA = 0.1 MPa. ATA: Atmosphere absolute. Support for an onset depth between 930 m and 1,080 m for the occurrence of psychotic-like disorders with the basic helium-oxygen mixture is the fact that no electroencephalographic epileptic patterns have been recorded in human divers at depths up to 701 m (71.1 ATA) and that convulsions in primates, while using much faster compression rates than those used in human divers, only occurred at around 1,000 m (101 ATA) (Bennett and Rostain, 1993). From this onset depth, if one considers (1) approximately 50 % of the divers participating to the dives in which psychotic-like narcotic episodes occurred were concerned by such symptoms, (2) it is only necessary to increase the minimal anesthetic concentration of common inhalational anesthetics (that is the concentration that produces anesthesia in 50% of subjects) by 10–15% to narcotize the vast majority of subjects (de Jong and Eger, 1975), it can be estimated that no human dives would be possible beyond 1,030–1,200 m (104–121 ATA) even in divers showing a low sensitivity to helium-oxygen narcosis. In conclusion, we suggest that improvement of the physical strategies used to reduce HPNS, such as slow compression rates with stages and adaptation with time at depth, may be the key for successfully going deeper, beyond the current world record human dives of 534 m (54.4 ATA) in the open sea and of 701 m (71.1 ATA) in hyperbaric chambers.
Table 1

Environmental conditions of absolute pressure and partial pressure of each inert gas during the experimental dives in which paroxysmal narcotic episodes occurred

Table 2

Partial molar volume and mole fraction solubility of the gases used during the experimental dives in which paroxysmal narcotic episodes occurred using benzene as a model of the gases’ hydrophobic site of action

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Review 1.  [Psycho-action of pressurized hydrogen. Apropos of 3 cases].

Authors:  Y Raoul; J C Douchet; A Trividic; J Gillard; P Cosson
Journal:  Ann Med Psychol (Paris)       Date:  1991-04       Impact factor: 0.380

2.  Evidence for inert gas narcosis mechanisms in the occurrence of psychotic-like episodes at pressure environment.

Authors:  J H Abraini
Journal:  Neuroreport       Date:  1995-11-27       Impact factor: 1.837

3.  Inert gas and raised pressure: evidence that motor decrements are due to pressure per se and cognitive decrements due to narcotic action.

Authors:  J H Abraini
Journal:  Pflugers Arch       Date:  1997-04       Impact factor: 3.657

4.  The physiological effects of hydrostatic pressure are not equivalent to those of helium pressure on Rana pipiens.

Authors:  B A Dodson; Z W Furmaniuk; K W Miller
Journal:  J Physiol       Date:  1985-05       Impact factor: 5.182

Review 5.  Effects of high pressure on the central nervous system.

Authors:  M J Halsey
Journal:  Physiol Rev       Date:  1982-10       Impact factor: 37.312

6.  Protein crystallography under xenon and nitrous oxide pressure: comparison with in vivo pharmacology studies and implications for the mechanism of inhaled anesthetic action.

Authors:  Nathalie Colloc'h; Jana Sopkova-de Oliveira Santos; Pascal Retailleau; Denis Vivarès; Françoise Bonneté; Béatrice Langlois d'Estainto; Bernard Gallois; Alain Brisson; Jean-Jacques Risso; Marc Lemaire; Thierry Prangé; Jacques H Abraini
Journal:  Biophys J       Date:  2006-10-06       Impact factor: 4.033

7.  Development of an organic affective syndrome during a hyperbaric diving experiment.

Authors:  A Stoudemire; J Miller; F Schmitt; P Logue; D Shelton; G Latson; P Bennett
Journal:  Am J Psychiatry       Date:  1984-10       Impact factor: 18.112

8.  Pressure reversal of general anaesthesia--a multi-site expansion hypothesis.

Authors:  M J Halsey; B Wardley-Smith; C J Green
Journal:  Br J Anaesth       Date:  1978-11       Impact factor: 9.166

9.  Nitrogen at raised pressure interacts with the GABA(A) receptor to produce its narcotic pharmacological effect in the rat.

Authors:  H N David; N Balon; J C Rostain; J H Abraini
Journal:  Anesthesiology       Date:  2001-10       Impact factor: 7.892

10.  Structural Basis for Xenon Inhibition in a Cationic Pentameric Ligand-Gated Ion Channel.

Authors:  Ludovic Sauguet; Zeineb Fourati; Thierry Prangé; Marc Delarue; Nathalie Colloc'h
Journal:  PLoS One       Date:  2016-02-24       Impact factor: 3.240

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