“…In addition to the aforementioned effects of EE and SE under physiological conditions, both interventions have been demonstrated to have therapeutic effects under pathological conditions. In this regard, both EE and SE induce recovery in various models of central nervous system injury (Berrocal et al, 2007;Gajhede Gram et al, 2015;Lajud et al, 2018). Moreover, EE increases AHN in mouse models of Down syndrome (Chakrabarti et al, 2011;Pons-Espinal et al, 2013), Alzheimer's disease (Levi and Michaelson, 2007;Mirochnic et al, 2009;Valero et al, 2011;Llorens-Martin et al, 2013;Marlatt et al, 2013), Huntington's disease (Lazic et al, 2006), diabetes (Pamidi and Nayak, 2014), ischemia (Rojas et al, 2013), and chronic pain (Zheng et al, 2017), after cranial irradiation (Garbugino et al, 2016), and during physiological aging (Kempermann et al, 1998(Kempermann et al, , 2002Kempermann, 2008Kempermann, , 2015Speisman et al, 2013).…”