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. 2021 Jan 7;11:7. doi: 10.1038/s41398-020-01156-y

Fig. 4. Chronic Activin A infusions into DG convert FLX non-responders into responders while chronic Inhibin A infusions convert responders into non-responders.

Fig. 4

a Timeline of experiment and coordinates of infusions for ventral DG and ventral CA1 infusions into FLX non-responders. b Kaplan–Meier survival curve (left panel) and scatterplot (right panel) of NSF data showing individual latency to eat values across all three FLX non-responder treatment groups: vehicle infusions into DG (VEHDG), Activin A infusions into DG (ACTIVINDG), and Activin A infusions into CA1 (ACTIVINCA1). ce One-Way ANOVA of VEHDG, ACTIVINDG, and ACTIVINCA1 for: EPM open arm entries and open arm duration (c), FST immobility (d), and Negative Affect Index (e). f Regression analyses correlating NSF latency to eat with EPM open arm duration (left) and FST immobility (right). g Timeline of experiment and coordinates of infusions for ventral DG and ventral CA1 infusions into FLX responders. h Kaplan–Meier survival curve (left panel) and scatterplot (right panel) of NSF data showing individual latency to eat values across all three FLX non-responder treatment groups: vehicle infusions into DG (VEHDG), Inhibin A infusions into DG (INHIBINDG), and Inhibin A infusions into CA1 (INHIBINCA1). One-Way ANOVA of VEHDG, INHIBINDG, and INHIBINCA1 for: EPM open arm entries and open arm duration (i), FST immobility (j), and Negative Affect Index (k). l Regression analyses correlating NSF latency to eat with EPM open arm duration (left) and FST immobility (right). For survival curves, line shading shows SEM of each group (n = 12 per group). Scatterplots, horizontal lines, and bars show group means with error bars indicating SEM.