During space flights, tadpoles of the clawed toad Xenopus laevisoccasionally develop upward bended tails (tail lordosis). The tail lordosis disappears after re-entry to 1g within a couple of days. The mechanisms responsible for the induction of the tail lordosis are unknown;physical conditions such as weight de-loading or physiological factors such as decreased vestibular activity in microgravity might contribute. Microgravity(μg) also exerts significant effects on the roll-induced vestibuloocular reflex (rVOR). The rVOR was used to clarify whether tail lordosis is caused by physiological factors, by correlating the occurrence ofμ g-induced tail lordosis with the extent of μg-induced rVOR modifications.

Post-flight recordings from three space flights (D-2 Spacelab mission,STS-55 in 1993; Shuttle-to-Mir mission SMM-06, STS-84 in 1997; French Soyuz taxi flight Andromède to ISS in 2001) were analyzed in these experiments. At onset of microgravity, tadpoles were at stages 25-28, 33-36 or 45. Parameters tested were rVOR gain (ratio between the angular eye movement and the lateral 30° roll) and rVOR amplitude (maximal angular postural change of the eyes during a 360° lateral roll).

A ratio of 22-84% of tadpoles developed lordotic tails, depending on the space flight. The overall observation was that the rVOR of tadpoles with normal tails was either not affected by microgravity, or it was enhanced. In contrast, the rVOR of lordotic animals always revealed a depression. In particular, during post-flight days 1-11, tadpoles with lordotic tails from all three groups (25-28, 33-36 and 45) showed a lower rVOR gain and amplitude than the 1g-controls. The rVOR gain and amplitude of tadpoles from the groups 25-28 and 33-36 that developed normal tails was not affected by microgravity while the rVOR of μg-tadpoles from the stage-45 group with normal tails revealed a significant rVOR augmentation. In conclusion: (1)the vestibular system of tadpoles with lordotic tails is developmentally retarded by microgravity; (2) after a critical status of vestibular maturation obtained during the appearance of first swimming, microgravity activates an adaptation mechanism that causes a sensitization of the vestibular system.

Tadpoles of the clawed toad Xenopus laevis subjected to gravity deprivation during space flights suffered behavioral and morphological modifications, which persisted for some days after termination of the space flight. Behavioral modifications included swimming abnormalities(Neubert et al., 1994; Snetkova et al., 1995; Fejtek et al., 1998) and a depression of both gain and amplitude of the roll-induced static vestibuloocular reflex (rVOR) (Sebastian et al., 1996) but not of the dynamic VOR induced by horizontal lateral displacements (Eßeling et al., 1994a; Eßeling et al., 1994b). Morphological modifications include a hyperextension of the tail (tail lordosis) (Fig. 1), and were observed in Xenopus laevis tadpoles launched before hatching (Snetkova et al.,1995; Sebastian and Horn,1998) but not in tadpoles that developed from eggs fertilized in orbit under microgravity (Souza et al.,1995) (cf. Table 1). After re-exposure to natural 1g conditions on the ground or to simulated 1g conditions in space by centrifugation, the tail lordosis disappeared during further development(Sebastian and Horn,1998).

The reduction of the rVOR is probably caused by developmental retardation of the vestibular system (Sebastian et al., 1996). Tail lordosis might be caused by weight de-loading during μg-exposure because affected tadpoles showed muscle degeneration (Snetkova et al.,1995). However, other factors such as: (1) trophic effects of vestibular activity on muscle development, and (2) the rostrocaudal maturation gradient, might cause tail lordosis if they revealed a sensitivity to altered gravity. In fact, vestibular activity of bullfrogs was transiently reduced during microgravity exposure (Bracchi et al., 1975). In addition, vestibular activity affects the development of extraocular eye muscles of juvenile rats(Brueckner et al., 1999). Activity-related trophic effects on developing neurons, their interneuronal connectivity patterns and the development of muscles were also described for the maturing visual system of fish, chick and rats(Schmidt, 1988; Fawcett, 1988). A rostrocaudal maturation gradient of the tail was described(Roberts and Tunstall, 1994). In addition, recordings from ventral roots of different tail segments during fictive swimming revealed a sensitivity of vestibulospinal projections to microgravity (Böser et al.,2003; Horn et al.,2003) and hypergravity(Böser and Horn, 2006)during early periods of tail development.

Thus, a rostrocaudal maturation gradient of the tail during early periods of life and a reduced or absent tonic vestibular activity may influence the development of vestibulospinal projections and body muscles, leading to transient modifications of body shape and locomotion, especially if the animals are exposed to an atypical environment such as microgravity. In deafferented bullfrog larvae, coupling between compensatory eye movements and locomotion was demonstrated (Stehouwer,1987). This close link between vestibuloocular and vestibulospinal mechanisms in tadpoles makes it reasonable to ask the question whether rVOR depression and tail lordosis are correlated due a basic mechanism.

During spaceflights, the g-level is 10-3g to 10-5g, but the term microgravity (microgravity; abbreviations μg or 0g) is used by the scientific community, and for convenience is so designated in this paper.

Tadpoles of the southern clawed toad Xenopus laevis Daudin were used from the stock of the Central Animal Holding Facility at the University of Ulm and from the Institute of Aerospace Medicine of the Deutsches Zentrum für Luftund Raumfahrt (DLR). The developmental stages were determined using published tables (Nieuwkoop and Faber, 1967). During the period of rVOR recordings, animals were kept in groups of five in small nets of 8 cm diameter at a temperature of 20°C.

Microgravity exposure

Tadpoles were exposed to microgravity during three space missions, the 10-day flight STS-55 (German D-2; 1993; experiment STATEX-VOR), the 9.2-day flight STS-84 (Shuttle-to-Mir SMM-06; 1997; experiment TADPOLES), and the 10-day flight Andromède (French Soyuz Taxi Flight to the International Space Station ISS; 2001; experiment AQUARIUS-XENOPUS). During the Spacelab mission D-2, animals were kept in groups of five in petriPERM dishes, which have a volume of 25 ml. At launch, they had reached stage 33-36, which is shortly before the hatching stage. For the flight on STS-84, animals were transported in groups of 12 in miniaquaria, which have a volume of 42 ml. They were launched when they had reached stage 25-28, which is the tail bud stage. Miniaquaria were developed for the flight on STS-84, and were re-used during the Andromède flight in 2001 when two different stages were exposed to microgravity. The young group had reached stage 26-27 at launch; they were kept in groups of 12 animals in each miniaquarium. Tadpoles from the old group had reached stage 45 at launch; at this time they were able to perform the rVOR. They were kept in groups of five in each miniaquarium.

During the D-2 and SMM-06 missions, a centrifuge for in-flight 1g-simulation was available (CC-groups). For all missions, a parallel ground control experiment (GG-groups) was performed. Tadpoles from the D-2 and the Andromède experiment were exposed to microgravity throughout the mission (MM-groups). During the SMM-06 experiment tadpoles were divided in four groups: (1) animals exposed to microgravity for 9.2 days(MM-group), (2) animals exposed to in-flight 1g-simulation for 93 h, and thereafter to microgravity for 5 days until re-entry to Earth-1g conditions (CM-group), (3) tadpoles treated in the opposite way (MC-group), and (4) animals exposed to in-flight 1g-simulation for the whole flight (CC-group)(Sebastian and Horn,1998).

For logistic reasons, animals from the D-2 mission were cooled for 4 days to 14°C to guarantee stage 33-36 at launch. Animals from the SMM-06 mission were always kept under laboratory temperature at a range of 22-24°C until handover to the launch team. Thereafter, they were stored at a temperature of 20°C for 17 h until launch. Animals from the Andromède mission were cooled for at least 2 days to 14°C to maintain the defined developmental stages of 26-27 and 45.

Recordings of the rVOR

A detailed description is given elsewhere(Horn et al., 1986; Sebastian et al., 1996). Briefly, the tadpoles were mechanically fixed in an observation chamber and illuminated homogeneously from the frontal view. They were rolled around their longitudinal axis by 360° in 15° steps. During this stimulation procedure, the animals were continuously videotaped. From these recordings,the posture of the eyes was determined 7 s after initiation of each 15°-step. The sine-like response characteristics were used to calculate the rVOR gain and rVOR amplitude (Fig. 2). The rVOR gain is defined by the ratio between the angular counter roll of the eye and the roll angle. In this study, data for a 30°roll from the horizontal to the inclined posture are presented. The rVOR amplitude is defined by the maximal eye movement during a complete 360°roll. Previous studies in Xenopus and the fish Oreochromis mossambicus have shown that the rVOR amplitude is a sensitive indicator to describe: (1) modifications of the rVOR during its development(Horn et al., 1986; Sebastian and Horn, 1999), (2)the extent of vestibular compensation after hemilabyrinthectomy(Rayer and Horn, 1986), and(3) susceptibility changes within the vestibuloocular system to altered gravity (Horn and Sebastian,1996; Sebastian et al.,1996; Sebastian and Horn,1998; Sebastian et al.,2001). Recordings of the rVOR were taken during the post-flight days 1-11 and also, in the case of the STS-84 study, 5 weeks after landing. Before starting the rVOR measurements, tadpoles were evaluated for their developmental stage and body shape.

Data evaluation and statistics

Animals were included in the statistical analysis only if they remained active for at least 3 h after the rVOR recording. During each recording period, each animal was investigated only once. Thus, each distribution of either rVOR gain or amplitude consists of statistically independent values. Some animals from the D-2 mission were tested twice with a delay of 7 days. Most animals from the SMM-06 mission could be tested twice during the first 2 post-flight weeks, and a third time 5 weeks later (cf. Table 2). Animals from the Andromède mission were always tested only once because they were later used for anatomical studies (Horn et al.,2006). The nonparametric U-test from Wilcoxon, Mann and Whitney (Sachs, 1997) was used because a transformation of the experimental distributions into a Gaussian one was not possible. Median values of samples are presented in tables. Lordotic and non-lordotic animals were compared with respect to: (1) their age (days after fertilization) and (2) their developmental stage [definition of stages(cf. Nieuwkoop and Faber,1967)], to exclude the impact of different developmental velocities for the occurrence of rVOR differences between lordotic and non-lordotic tadpoles. Frequency distributions determined to describe the developmental progress during μg-exposure were tested by means of the χ2-test(Sachs, 1997).

During all missions, Xenopus embryos continued to develop. However, lordotic animals revealed slightly smaller developmental progress(Table 1) than normally developed ones. For example, during the first and fourth post-flight day both the lordotic animals from the MM- and CM-groups from the SMM-06 mission developed to stage 47.0, and the corresponding non-lordotic tadpoles to stages 47.1 and 47.2, respectively. The MC-, CC- and 1g-ground tadpoles had reached the stages 47.1, 47.0 and 47.1, respectively. The stage differences between flight and ground tadpoles were not significant(χ2-test: P>0.05). The stage difference became larger during the second week of recordings and reached values of 0.6 for the MM-group and 1.3 for the CM-group. For tadpoles from the missions D-2 and Andromède, the absolute stage differences never exceeded 0.3(Table 1).

Frequency of lordosis

In most tadpole groups from the D-2, Shuttle-to-Mir (cf. Fig. 1) and Andromède missions that were exposed to microgravity, lordotic animals could be observed after landing. The only exception was the MC-group from SMM-06, which was first exposed to microgravity and, thereafter, to 1g-conditions by centrifugation during the space flight(Table 1). In-flight observations of the tadpoles during flight day FD4 (mission elapse time MET 3/3:27 to 3/3:46) and FD9 (MET 7/21:40 to 7/22:8) during SMM-06 were recorded for each 12 animals from the 1g-inflight control andμ g-groups (MM, CM and MC). These recordings revealed abnormal tail development even at FD4 in the μg-reared groups MM and MC, but not in CM. On FD9, some tadpoles from the CM group had lordotic tails as well as those from the MM tadpoles while no lordotic animal was observed in the MC-group. As demonstrated by the in-flight video recordings, lordotic tadpoles were also observed during the Andromède mission on FD4 and FD9.

Due to the large number of available animals after landing, recovery from tail lordosis could be studied for tadpoles from SMM-06. In the MM-group, 25 out of 34 tadpoles revealed lordosis 4 days after landing of the spacecraft,while 14 days after landing, only one out of 28 tadpoles was lordotic. In the CM-group of this mission, the respective ratios were 13 out of 28 at post-flight day 4 and one out of 23 at post-flight day 14(Table 1). These data fit with the observations from in-flight video recordings, which revealed that lordosis developed during the first 4 days in microgravity disappeared if these tadpoles were exposed to 1g-centrifugation during the remaining 5 days of the flight (MC-group).

Tail lordosis and vestibuloocular reflex

Logistic and developmental conditions make it impossible to follow the rVOR of individual animals during the complete experiment starting before onset and ending after termination of microgravity conditions. Therefore, all observations about modifications of the rVOR are related to a comparison of means of respective samples. Based on this limitation, the overall observation of the experiments was that the rVOR values of tadpoles with normal tails were either not affected by microgravity, or enhanced. In contrast, lordotic animals always revealed a depression of their rVOR(Table 2).

Tadpoles from the Shuttle-to-Mir mission SMM-06

The tadpoles of this flight had reached stage 25-28 at launch. After landing of the spacecraft, tail lordosis was observed only in the MM- and CM-groups. Tadpoles from the other three experimental groups MC, CC and GG,had developed normal tails. For all groups, rVOR recordings were taken 3 times in most animals, the first between post-flight days 1-4, and the last between post-flight days 38-41.

During the first recording period, the rVOR was depressed only in tadpoles with lordotic tails. Normally developed MM-tadpoles had nearly the same median rVOR amplitude as the other groups without or short microgravity experience(MM: 51.9°; GG: 52.0°; CC: 47.8°; note that CC-animals were exposed to microgravity for about 20% of the mission because the 1g-centrifuge was started not before FD2, and switched off 12 h before landing). However, within samples with microgravity experience that contained lordotic and normal tadpoles, the rVOR amplitude was always smaller in lordotic than in normal animals (MM-group: 35.9° vs 51.9°, P<0.01; CM-group: 45.9° vs 54.1°, P<0.02) (Fig. 3). For the rVOR gain, the observations were similar; however, the gain differences between lordotic and normal animals were never significant(Fig. 4).

During the second post-flight recording period, lordotic tails were still present in both MM- and CM-tadpoles but in a lower number of tadpoles. However, the number of tadpoles with normal tails was higher then during the first recording, i.e. normalization of tail development took place. The tadpoles with lordotic tails revealed a reduced rVOR performance compared to normally developed tadpoles with μg-experience. These differences were significant for both rVOR amplitude (MM-group: 36.0° vs 53.8°, P<0.002; CM-group: 36.3° vs61.2°, P<0.01) and rVOR gain (MM-group: 0.228 vs0.392, P<0.01; CM-group: 0.325 vs 0.529, P<0.02) (Fig. 4). Five weeks after landing, both rVOR gain and rVOR amplitude were on the same level for all five groups. At that time, only tadpoles with normal tails were alive.

Comparison of the median rVOR amplitudes and gains in the time frame revealed developmental progress of the rVOR in all groups, but only for tadpoles with normal tails. During the period between the first and third recording period, the median values for the rVOR amplitude recorded for all five experimental groups MM, MC, CM, CC and GG, increased from a range between 45.8° and 54.1° to a range between 71.5° and 78.0°(Fig. 3). In most groups, the developmental progress of the rVOR amplitude from one to the next recording period was significant except for the lordotic and normal MM-groups between the first and second recording period. Similar to the rVOR amplitude, the rVOR gain also increased from the first to the third recording period. But due to larger variations of data, these increases are often not significant,especially for tadpoles with microgravity experience during the second 4.5-day period of the mission (Table 2; Fig. 4). Lordotic tadpoles could be observed only for 2 weeks after landing. In contrast to the normal animals, they never revealed a significant change of the rVOR between the first and second recording period; instead, both rVOR and rVOR gain declined(Figs 3 and 4).

The rVOR depression was not related to a general retardation in development. Comparison between the rVOR amplitude in stage-matched samples revealed a weaker response of lordotic compared to normal tadpoles. This result was clearly demonstrated for the rVOR amplitude in the MM-group. For both stage-47 and stage-48 tadpoles, the lordotic animals always revealed a lower rVOR amplitude than for tadpoles with normal tails (MM stage 47:35.2° vs 53.1°, P<0.002; MM stage 48: 39.6° vs 52.0°, P<0.05). The difference was less pronounced or absent for the rVOR gain (Fig. 5).

Tadpoles from the STS-55 (D-2) mission

Experiments from this particular mission have recently been published(Sebastian et al., 1996). However in the context of the observations from the Shuttle-to-Mir experiment,the data were re-evaluated with respect to correlations between occurrence of tail lordosis and rVOR expression. Due to the lower number of specimens, the chances of seeing significant differences were low; however, the available data clearly show tendencies in the same direction as observed after SMM-06:depression of the rVOR in lordotic tadpoles but no microgravity effect in normally developed ones. In particular, the rVOR amplitudes from the ground controls always differed significantly from those recorded from lordotic animals for both recording periods. This also held for the in-flight 1g-control (Fig. 6A,B). Normal vs lordotic tadpoles of the microgravity group always revealed lower rVOR amplitudes in the lordotic animals, but the differences can only be considered as a trend for the second recording period(normal: 18.7° vs 48.8°, P<0.1; N=3 for each sample). Similar observations were obtained for the rVOR gain(Fig. 6C,D).

Tadpoles from the Andromède mission to the International Space Station

At launch, embryos had reached stages 26-27 and tadpoles stage 45. During this mission, specimen from both stage groups developed lordotic tails. The number was low but high enough to get reliable statistical conclusions. The main result was that the stage 26-27 group confirmed the observations from the SMM-06 mission. Lordotic tadpoles revealed the significant depression of the rVOR amplitude while normally developed animals performed the rVOR at the same median level as did 1g controls (μg:18.1° vs 33.2°, P<0.02). In the stage-45 groups,lordotic tadpoles revealed a depressed rVOR (μg: 29.2 vs 43.0°; P=0.05) while normally developed animals showed a significant augmentation of the rVOR (μg: 43.0;1g: 33.0; P<0.02)(Fig. 7). Significant differences were also obtained for the rVOR gain. The augmentation of the rVOR in microgravity tadpoles with respect to the 1g-ground controls resembled the observation in fish (Oreochromis mossambicus)after a 9-day space flight and points to a sensitization of the neuronal network underlying the rVOR (Sebastian et al., 2001).

The present study shows a clear correlation between the occurrence of microgravity-induced tail lordosis and a depression of the roll-induced vestibuloocular reflex (rVOR). Tail lordosis was accompanied by a depression of the rVOR, while normal development of the body in microgravity was accompanied by no rVOR modification in those tadpoles launched at embryonic stages before hatching (Figs 3, 4, 6 and 7, upper plot) or with an augmentation of the rVOR in tadpoles launched when they have already developed their rVOR (Fig. 7, lower plot). Tail lordosis was first described as some kind of body malformation(Sebastian and Horn, 1998)based on the de-loading effects on muscles in microgravity(Snetkova et al., 1995). However, in the context of the observation that tail lordosis is coupled with a depression of the rVOR, neurophysiological components need to be taken into consideration. These might include (1) a general developmental retardation and loss of synchrony in the rostrocaudal developmental gradient of the motor tail system [this gradient was described elsewhere(Roberts and Tunstall, 1994)]as well as (2) a lack or failure of trophic effects of vestibular activity in microgravity. A completely different approach for the understanding of the microgravity effects on body shape and rVOR comes from a consideration of a microgravity susceptibility of secreted growth factors.

Neurophysiological aspects of tail lordosis and rVOR development

A striking observation was that in contrast to normally developing tadpoles, lordotic animals revealed no developmental progress in their rVOR during the observation period of 11 days after termination of microgravity exposure (Figs 3, 4 and 6) in spite of morphological progression as determined by the external morphological markers(Nieuwkoop and Faber, 1967). In some instances, normally developed stage 47 tadpoles performed a stronger rVOR than lordotic stage 48 animals (Fig. 5, upper plots). This observation points to a significant retardation of vestibular development in the lordotic animals.

In Xenopus laevis, swimming and the underlying neuronal network develop when animals have reached stages 27 to 33. This early developmental period is characterized by a rostrocaudal maturation gradient(van Mier, 1988; van Mier et al., 1989), and the separation of the ear vesicle. During this period, the proper development of the vestibular system is initiated and the vestibuloocular system becomes functionally sensitive to macular stimulation by stage 42(Horn et al., 1986)[definition of developmental stages in Xenopus (see Nieuwkoop and Faber, 1967)]. Thus, there is a clear overlap in the development of the spinomotor,vestibular and vestibuloocular system that requires and/or causes a tuning between these developing systems at this period of life to produce a physiologically stable organism. In fact, observations in deafferented bullfrog larvae revealed coordination between ocular counter roll and motor activity in the spinal ventral roots(Stehouwer, 1987). Environmental disturbances such as microgravity might disrupt - in some embryos - this coupling, leading to different morphological and physiological expressions of these systems, as demonstrated by the depressed rVOR and tail lordosis that contrasts the coupling of normal tail development with normal rVOR development (Figs 3, 4, 5, 6, 7). Thus, a coordinated development of spinal and oculomotor systems under standard earth conditions might require normal vestibular activity as a neurotrophic factor, which is known from the development of extraocular eye muscles in rats(Brueckner et al., 1999).

It was shown earlier that motor development of Xenopus embryos continued independently of functional activity(Haverkamp, 1986). Embryos immobilized by chloretone or lidocain during a period between the late neurula stage and the time of hatching demonstrated normal motor output in the spinal ventral roots during fictive swimming and normal size of motor neurons and their dendritic arborization. However, space tadpoles developed in a freely moving condition. They were active during their exposure to microgravity and,in fact, they revealed an increased motor activity compared to their ground controls (Dournon et al.,2002).

The most likely mechanism for reflex augmentation in the older tadpoles(cf. Fig. 7) is sensitization of the vestibular system by gravity deprivation, as also shown in bullfrogs(Bracchi et al., 1975), fish(Boyle et al., 2000; Sebastian et al., 2001; Wiederhold et al., 2003) and men (Clément et al.,2001). Recordings from the vestibular nerve of bullfrogs during microgravity revealed an initial depression of spontaneous activity but a recovery and overcompensation during ongoing microgravity exposure(Bracchi et al., 1975). Assuming a similar process in the normally developing tadpoles, this recovery and overcompensation of vestibular baseline activity sensitizes the vestibular system and thus augments the reflex after re-entry into 1g-conditions.

Distribution of secreted growth factors and tail lordosisrVOR relations

Developmental processes such as axis formation are strongly affected by the distribution of growth factors. Any disturbance of this gradient can cause morphological modifications, including the body shape (cf. Gilbert, 2003). The neural tube revealed dorsoventral gradients of secreted growth factors. For example,a gradient from a Wnt and BMP (bone morphogenetic proteins) source dorsalizes the neuroectoderm while a BMP antagonist and Shh (Sonic hedgehog) source at the notochord reveals ventralizing features(Wilson and Edlung, 2001; Wessely and De Robertis,2002). Interestingly, Xenopus tadpoles with tail lordosis show notochord abnormalities due to microgravity exposure during space flight(Snetkova et al., 1995). In fact, preliminary studies in Xenopus demonstrated a correlation between growth factor and rVOR modification. It was shown that knock-down of the transcription factor Tcf-4 of the Wnt-pathway by morpholino injection in one cell of the 2-cell stage caused tail lordosis and, additionally,depression of the rVOR (Horn et al.,2005). This morpholino-induced lordosis cannot be attributed to a Wnt pathway defect alone because in general, a balance of Wnts, BMPs, and Shh expression levels and patterns determines the establishment of the body axes. Knocking down the level of one factor would give a phenotype similar to the overexpression of one of the other factors. Interestingly, the dorsal/ventral axis of the inner ear is also patterned by a balance of Wnt and Shh(Riccomagno et al., 2005),i.e. the observed modifications of the vestibular system could also be due to Shh overexpression. In conclusion, if microgravity is a disturbing factor of secreted growth factors involved in axis formation, the development of ocular and spinal projections and thus, the development of the rVOR and tail, are probably affected by a spaceflight.

This work was supported by Deutsches Zentrum für Luftund Raumfahrt(DLR), grants no. 01QV8925-5, 50WB9553-7 and 50WB0140. I thank the BIONETICS team for experimental support at Hangar L/Kennedy Space Center in 1993 and 1997, and the CNES team and, in particular, Dr Michel Viso and Didier Chaput for technical and logistic support during the Andromède mission, the ESA, OHB/Bremen and EADS Space Transportation (former Dornier)/Friedrichshafen teams for technical support during the D-2 and SMM-06 missions, my co-workers Sybille Böser, Konrad Eßeling and Claudia Sebastian for their help during the performance of the experiments during the missions and during the rVOR recordings and analysis, and the Crews of STS-55, STS-84 and the Andromède mission for their careful handling of animal samples and equipment during the flights. All experiments comply with the `Principles of Animal Care', publication No. 86-23, revised 1985 of the National Institutes of Health, and with the `Deutsches Tierschutzgesetz', BGBl from February 17,1993. Permission for the experiments was given by the Regierungspräsidium of Tübingen (Germany), no. 399/Ulm, no. 506/Ulm and 657/Ulm, as well as by the Animal Care and Use Committee (ACUC) at Kennedy Space Center/Florida.

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