Corrigendum: What can the common fruit fly teach us about stroke?: lessons learned from the hypoxic tolerant Drosophila melanogaster.

[This corrects the article DOI: 10.3389/fncel.2024.1347980.].

What can the common fruit fly teach us about stroke?: lessons learned from the hypoxic tolerant Drosophila melanogaster.

Stroke, resulting in hypoxia and glucose deprivation, is a leading cause of death and disability worldwide. Presently, there are no treatments that reduce neuronal damage and preserve function aside from tissue plasminogen activator administration and rehabilitation therapy. Interestingly, Drosophila melanogaster, the common fruit fly, demonstrates robust hypoxic tolerance, characterized by minimal effects on survival and motor function following systemic hypoxia. Due to its organized brain, conserved neurotransmitter systems, and genetic similarity to humans and other mammals, uncovering the mechanisms of Drosophila's tolerance could be a promising approach for the development of new therapeutics. Interestingly, a key facet of hypoxic tolerance in Drosophila is organism-wide metabolic suppression, a response involving multiple genes and pathways. Specifically, studies have demonstrated that pathways associated with oxidative stress, insulin, hypoxia-inducible factors, NFκB, Wnt, Hippo, and Notch, all potentially contribute to Drosophila hypoxic tolerance. While manipulating the oxidative stress response and insulin signaling pathway has similar outcomes in Drosophila hypoxia and the mammalian middle cerebral artery occlusion (MCAO) model of ischemia, effects of Notch pathway manipulation differ between Drosophila and mammals. Additional research is warranted to further explore how other pathways implicated in hypoxic tolerance in Drosophila, such as NFκB, and Hippo, may be utilized to benefit mammalian response to ischemia. Together, these studies demonstrate that exploration of the hypoxic response in Drosophila may lead to new avenues of research for stroke treatment in humans.

Progesterone receptor expression in the brain of the socially monogamous and paternal male prairie vole.

Differences in the social organization and behavior of male mammals are attributable to species differences in neurochemistry, including differential expression of steroid hormone receptors. However, the distribution of progestin receptors (PR) in a socially monogamous and spontaneously parental male rodent has never been examined. Here we determined if PR exists and is regulated by testicular hormones in forebrain sites traditionally influencing socioreproductive behaviors in male prairie voles (Microtus ochrogaster). We hypothesized that PR expression in male prairie voles would differ from that described in other male rodents because PR activity inhibits parental behaviors and social memory in laboratory mice and rats. Adult male prairie voles received a sham surgery, were gonadectomized, or were gonadectomized and implanted with a testosterone-filled capsule. PR immunoreactivity (PRir) was measured four weeks later in areas of the hypothalamus and extended amygdala. A group of gonadally intact female prairie voles was included to reveal possible sex differences. We found considerable PRir in all sites examined. Castration reduced PRir in males' medial preoptic nucleus, anteroventral periventricular nucleus, ventromedial hypothalamus, and posterodorsal medial amygdala, and it was maintained in these sites by testosterone. This is the first study to examine PR expression in brain sites involved in socioreproductive behaviors in a socially monogamous and spontaneously paternal male rodent. Our results mostly reveal cross-species conservation in the distribution and hormone sensitivity of PR expression. Because PR interferes with aspects of sociality in other male rodents, PR may eventually be found to have different neurobiological actions in male prairie voles.