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Effects of progesterone on male-mediated infant-directed aggression
Johanna S Schneider1, Carly Burgess, Teresa H Horton
1Northwestern University, Department of Neurobiology and Physiology, 2205 Tech Drive, Evanston, IL 60208, United States.
Insights
Progesterone (P) withdrawal does not induce parental behavior in male mice. Prior exposure to P, however, leads to persistent infanticidal behavior, revealing a novel mechanism for aggression regulation.
Area of Science:
- Neuroscience
- Behavioral Biology
- Endocrinology
Background:
- Parental behavior and infanticide are observed in many species.
- The neural regulation of transitions between parental care and infanticide is not well understood.
- Progesterone (P) and its receptor (PR) inhibit parental behavior and promote infanticide in male mice.
Purpose of the Study:
- To investigate the mechanisms underlying progesterone's effects on male mouse behavior.
- To test the hypothesis that progesterone withdrawal, similar to female pregnancy, enhances parental behavior in males.
- To determine if progesterone withdrawal triggers the onset of parental behavior in adult male mice.
Main Methods:
- Virgin male mice were administered progesterone (P) or vehicle for 21 days.
- Behavioral tests for parental care and infanticide were conducted 5 days post-treatment.
- Serum levels of P and testosterone (T) were measured at the time of behavioral testing.
Main Results:
- Progesterone treatment increased the proportion of males exhibiting infanticide towards pups.
- Neither parental care initiation nor quality was affected by progesterone treatment.
- Serum P and T levels did not differ between groups, indicating ongoing hormone elevation is not required for infanticide.
Conclusions:
- Progesterone withdrawal does not initiate parental behavior in male mice.
- Prior exposure to progesterone induces persistent infanticidal behavior in adult male mice.
- This suggests a mechanism where prior hormonal exposure, not withdrawal, influences aggressive behaviors.
Abstract:
Many species that engage in parental behavior exhibit infanticide under certain circumstances. The neural signals regulating the transition from infant care giver to infant killer and back remain unclear. Previously we demonstrated that progesterone (P) and its receptor (PR) have inhibitory effects on parental behavior and increase infant-directed aggression in male mice. In the present studies we sought to elucidate the mechanisms by which the effects of P are manifested. Because the onset of parental behavior in females is associated with the withdrawal of P at the end of pregnancy we tested the hypothesis that withdrawal of P would similarly enhance parental behavior in males. Virgin male mice were implanted with P or vehicle for 21 days, replicating the duration of pregnancy in females. Tests were run for parental and infanticidal behavior 5 days after removal of the capsules. P increased the proportion of nonparental males that attacked pups. However, neither the number of males exhibiting parental care nor the quality of care was affected by P treatment. Serum P and testosterone (T) levels were not different from controls at the time of behavioral testing indicating continued elevations in peripheral hormones are not required for the expression of infanticide. In conclusion, withdrawal of P does not trigger the onset of parental behavior in males. Rather, prior exposure to P induces persistent infanticidal behavior in adult male mice.
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