Simulated weightlessness procedure, head-down bed rest impairs adult neurogenesis in the hippocampus of rhesus macaque
The microgravity environment in space can impact astronauts’ cognitive and behavioral activities. However, due to the limitations of research conditions, studies of biological changes in the primate brain, such as neurogenesis, have been comparatively few. We take advantage of − 6° head-down bed rest (HDBR), one of the most implemented space analogue on the ground, to investigate the effects of weightlessness on neurogenesis of non-human primate brain. Rhesus Macaque monkeys were subjected to HDBR for 42 days to simulate weightlessness. BrdU (5-bromodeoxyuridin) and IdU (iododeoxyuridine) were intraperitoneally injected separately before or after HDBR to label the survival and proliferation of newborn neurons. Immunohistochemistry was performed to study the effect of simulated weightlessness on neurogenesis. BrdU staining showed that survival of newborn neurons was reduced, while there were fewer BrdU-positive neurons in the HDBR group compared with the control. Furthermore, IdU-positive neurons also decreased in the HDBR group suggesting a reduced proliferation capacity for these newborn neurons. Our results demonstrate the definite neurogenesis in the adult rhesus macaque hippocampus, and simulated weightlessness HDBR procedure impairs the adult neurogenesis.
KeywordsAdult neurogenesis Simulated weightlessness Rhesus monkey
Head-down bed rest
Phosphate buffered saline
There have been many long-duration spaceflights over the past decades, and more spaceflights with even longer durations will be required in the future. Humans, instead of robots, have an essential role in long-duration spaceflight missions due to superior perception, intelligent decision-making and capacity for independent action. It is clear that the microgravity environment in space can impact astronauts’ cognitive and behavioral activities [1, 2], which further affects the astronauts’ decision-making . This could be noteworthy risk for long-duration spaceflight missions. Therefore, it is of great importance to reveal the underlying mechanism of how microgravity leads to abnormal cognitive and behavioral activities. Physiology studies reveal that changes in volumes of cerebrospinal fluid, cerebral blood flow and intracranial pressure are caused by the redistribution of an astronaut’s body fluid toward the head in a weightless environment [4, 5], and this may lead to structure remodeling. Neuroimaging studies have demonstrated alterations in the volumes of gray matter and white matter in specific brain regions including the frontal lobes and the hippocampus . Early studies have also shown microgravity affects neurotransmitter concentrations  and the number of synapses .
In this study, 5 monkeys were subjected to HDBR for 42 days to study the effects on the brain. Simultaneously, monkeys in the control group were single housed in the cages in the next room. While muscle atrophy and bone loss were also studied, those results are outside the scope of this paper. We collected tissue from the monkeys to examine whether HDBR for 42 days had an influence on adult hippocampal neurogenesis. Both BrdU (5-bromodeoxyuridin) and IdU (iododeoxyuridine) were intraperitoneally injected to label the newborn neurons. BrdU was injected before HDBR, while IdU was injected at the end of HDBR (Fig. 1b). Two primary antibodies, rat anti-BrdU (react with BrdU only) and mouse anti-BrdU(react with BrdU and IdU), were used for the separation of BrdU and IdU. BrdU-positive and IdU-positive cells in dentate gyrus (DG) were counted to represent the capacity of neurogenesis. We found significant reduction of cell survival by BrdU labeling (HDBR, N = 5, control, N = 3) and decreased cell proliferation by IdU labeling (HDBR, N = 5, control, N = 4) in HDBR group compared with the control (Fig. 1c-e and Additional file 1: Table S1). These results demonstrated that 42 days HDBR impairs adult hippocampal neurogenesis.
Hippocampal neurogenesis has been observed in different adult animals. Studies have indicated that the newly generated cells might have a function in cognition and brain repair . Adult hippocampal neurogenesis is also found in humans and contributes to memory function and enhanced synaptic plasticity across the life span. Adult hippocampal neurogenesis adds particular functionality to the mammalian hippocampus and presumably is involved in cognitive functions that we consider to be essential for humans . Recent research found that recruitment of young neurons to the primate hippocampus decreases rapidly during the first years of life, and neurogenesis in the DG is extremely rare in adult , however, our results strongly prove that adult neurogenesis was still continued in adult monkeys.
During HDBR procedure, the monkeys were restrained on the bed. Several studies showed that volunteers developed psychic stress, and the plasm hormone involved in the response of the organism to stress, such as cortisol was significantly altered in human HDBR research . Restraint stress has also been related to decreased cell proliferation and survival of the newborn hippocampal granule cells in mice. . The decreased neurogenesis was caused by HDBR procedure, which might contain the effects from cephalic fluid shift and stress.
In conclusion, our results indicated the unambiguous neurogenesis in the adult rhesus macaque hippocampus, and simulated weightlessness HDBR procedure impairs the adult neurogenesis.
The authors are grateful to all those who participated in this research for their contributions.
This work was supported by, National Natural Science Foundation of China (NSFC) 91632103, Program of Shanghai Subject Chief Scientist 17XD1401700, Shanghai Education Commission Research and Innovation Program 2019-01-07-00-02-E00037, “111” Program of Higher Education Discipline Innovation, “Eastern Scholar” (Shanghai Municipal Education Commission) and National Natural Science Foundation of Liaoning Province 201602233.
Availability of data and materials
All data generated or analyzed during this study are included in this article and Additional file1.
WL and XC* designed the experiments. XZ, XC#, LC and WL wrote the article. All authors participated in the experiments or data analyze. All authors read and approved the final manuscript.
All procedures were performed in accordance with the principles of the Association for Assessment and Accreditation of Laboratory Animal Care International (AAALAC), approved by Institutional Animal Care and Use Committee of China Astronaut Research and Training Center (ACC-IACUC-2014-001) and Institutional Animal Care and Use Committee of Shanghai Jiao Tong University (IACUC-20140710).
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The authors declare that they have no competing interests.
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