Well your doctor has a lot of studying to do.
Well your doctor has a lot of studying to do.
The latest here:
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1Penn State University- Altoona campus, USA
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2Franklin & Marshall College, USA
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3Hamilton College, USA
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4University of California- Santa Cruz, USA
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5University of Nevada, Reno, USA
Variation in an animal’s spatial environment can induce
variation in the hippocampus, an area of the brain involved in spatial
cognitive processing. Specifically, increased spatial area use is
correlated with increased hippocampal attributes such as volume and
neurogenesis. In the side-blotched lizard (Uta stansburiana), males
demonstrate alternative reproductive tactics and are either territorial -
defending large, clearly defined spatial boundaries - or
non-territorial - traversing home ranges that are smaller than the
territorial males’ territories. Our previous work demonstrated cortical
volume (reptilian hippocampal homologue) correlates with these spatial
niches. We found that territorial holders have larger medial cortices
than non-territory holders, yet these differences in the neural
architecture demonstrated some degree of plasticity as well. Although we
have demonstrated a link among territoriality, spatial use, and brain
plasticity, the mechanisms that underlie this relationship are unclear.
Previous studies found that higher testosterone levels can induce
increased use of the spatial area and can cause an upregulation in
hippocampal attributes. Thus, testosterone may be the mechanistic link
between spatial area use and the brain. What remains unclear, however,
is if testosterone can affect the cortices independent of spatial
experiences and whether testosterone differentially interacts with
territorial status to produce the resultant cortical phenotype. In this
study, we compared neurogenesis as measured by the total number of
doublecortin-positive cells and cortical volume between territorial and
non-territorial males supplemented with testosterone. We found no
significant differences in the number of doublecortin-positive cells or
cortical volume among control territorial, control non-territorial, and
testosterone-supplemented non-territorial males, while
testosterone-supplemented territorial males had smaller medial cortices
containing fewer doublecortin-positive cells. These results demonstrate
that testosterone can modulate medial cortical attributes outside of
differential spatial processing experiences but that territorial males
appear to be more sensitive to alterations in testosterone levels
compared with non-territorial males.
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