The structure and function of the brain greatly rely
on different
signaling pathways. The wide variety of biological processes, including
neurogenesis, axonal remodeling, the development and maintenance of
pre- and postsynaptic terminals, and excitatory synaptic transmission,
depends on combined actions of these molecular pathways. From that
point of view, it is important to investigate signaling pathways and
their crosstalk in order to better understand the formation of toxic
proteins during neurodegeneration. With recent discoveries, it is
established that the modulation of several pathological events in
Alzheimer’s disease (AD) due to the mammalian target of rapamycin
(mTOR), Wnt signaling, 5′-adenosine monophosphate activated
protein kinase (AMPK), peroxisome proliferator-activated receptor
gamma coactivator 1α (PGC-1α), and sirtuin 1 (Sirt1, silent
mating-type information regulator 2 homologue 1) are central to the
key findings. These include decreased amyloid formation and inflammation,
mitochondrial dynamics control, and enhanced neural stability. This
review intends to emphasize the importance of these signaling pathways,
which collectively determine the fate of neurons in AD in several
ways. This review will also focus on the role of novel synthetic and
natural bioactive molecules in balancing the intricate crosstalk among
different pathways in order to prolong the longevity of AD patients.