Bodovitz Steven
BioPerspectives, 2040 Hyde Street, San Francisco, CA 94109, USA.
J Theor Biol. 2008 Oct 7;254(3):594-8. doi: 10.1016/j.jtbi.2008.04.019. Epub 2008 Apr 22.
I propose that we are only aware of changes in our underlying cognition. This hypothesis is based on four lines of evidence. (1) Without changes in visual input (including fixational eye movements), static images fade from awareness. (2) Consciousness appears to be continuous, but is actually broken up into discrete cycles of cognition. Without continuity, conscious awareness disintegrates into a series of isolated cycles. The simplest mechanism for creating continuity is to track the changes between the cycles. (3) While these conscious vectors are putative, they have a clear source: the dorsolateral prefrontal cortex (DLPFC). The DLPFC is active during awareness of changes, and this awareness is disrupted by repetitive transcranial magnetic stimulation. (4) When the DLPFC and the orbital and inferior parietal cortices are deactivated during dreaming, conscious awareness is absent even though the rest of the brain is active. Moreover, Lau and Passingham showed that activation of the DLPFC, but no other brain region, correlates with awareness. In summary, if the DLPFC and conscious vectors are the neural correlate of consciousness, then we are only aware of changes in our underlying cognition. The glue that holds conscious awareness together is conscious awareness.
我提出,我们仅能察觉到潜在认知的变化。这一假设基于四条证据。(1)在视觉输入无变化(包括注视性眼动)的情况下,静态图像会从意识中消退。(2)意识看似是连续的,但实际上是被分解为离散的认知周期。没有连续性,意识觉知就会瓦解为一系列孤立的周期。创造连续性的最简单机制是追踪周期之间的变化。(3)虽然这些意识向量是推测性的,但它们有一个明确的来源:背外侧前额叶皮层(DLPFC)。在察觉到变化时,DLPFC会被激活,而这种觉知会被重复经颅磁刺激所扰乱。(4)在做梦期间,当DLPFC以及眶额和顶下叶皮层失活时,即使大脑的其他部分处于活跃状态,意识觉知也不存在。此外,刘和帕辛厄姆表明,DLPFC的激活与觉知相关,而其他脑区则不然。总之,如果DLPFC和意识向量是意识的神经关联物,那么我们仅能察觉到潜在认知的变化。将意识觉知维系在一起的粘合剂就是意识觉知。