Opioid-dependent growth of glial cultures: Suppression of astrocyte DNA synthesis by met-enkephalin
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Glial neuroimmune signaling in opioid reward
2020, Brain Research BulletinCitation Excerpt :Another possible reason may be due to the traditional notion that the activation of opioid receptors is immunosuppressive, which is opposite to the observation of opioid-mediated glial activation (Liang et al., 2016a). This view is supported by several studies demonstrating the activation of opioid receptors can functionally inhibit glial cells (Chao et al., 1997; Hansson et al., 2008; Hu et al., 2000, 1998; Stiene-Martin and Hauser, 1993, 1990). Nevertheless, other studies indicate that opioid receptors exert stimulatory effects on the immune system (Liang et al., 2016b; Muscoli et al., 2010).
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2019, Progress in Neuro-Psychopharmacology and Biological PsychiatryCitation Excerpt :Multiple mechanisms may be involved in the astrocytic response to opioids, including glucocorticoids (Slezak et al., 2013), TLR4/lipopolysaccharide signaling (Hutchinson et al., 2012), or direct activation via opioid receptors expressed by astrocytes (Ruzicka et al., 1995; Stiene-Martin et al., 2001). Paradoxically, this contradicts earlier findings showing that morphine and other opioids inhibit DNA synthesis and cellular maturation of astrocytes in tissue culture (Stiene-Martin et al., 1991; Stiene-Martin and Hauser, 1990, 1991, 1993). This is likely indicative of key modulatory factors present in vivo which are lost in cell culture studies.
Thyroid hormones protect astrocytes from morphine-induced apoptosis by regulating nitric oxide and pERK 1/2 pathways
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