Prostaglandin F2α Affects the Cycle of Clock Gene Expression and Mouse Behavior.
Yuya TsurudomeYuya YoshidaKengo HamamuraTakashi OginoSai YasukochiShinobu YasuoAyaka IwamotoTatsuya YoshiharaTomoaki InazumiSoken TsuchiyaNobuyuki MikodaNaomi NakagataShigekazu HiguchiYukihiko SugimotoAkito TsurutaSatoru KoyanagiNaoya MatsunagaShigehiro OhdoPublished in: International journal of molecular sciences (2024)
Prostaglandins are bioactive compounds, and the activation of their receptors affects the expression of clock genes. However, the prostaglandin F receptor ( Ptgfr ) has no known relationship with biological rhythms. Here, we first measured the locomotor period lengths of Ptgfr-KO (B6.129- Ptgfr tm1Sna ) mice and found that they were longer under constant dark conditions (DD) than those of wild-type (C57BL/6J) mice. We then investigated the clock gene patterns within the suprachiasmatic nucleus in Ptgfr-KO mice under DD and observed a decrease in the expression of the clock gene cryptochrome 1 ( Cry1 ), which is related to the circadian cycle. Moreover, the expression of Cry1 , Cry2 , and Period2 ( Per2 ) mRNA were significantly altered in the mouse liver in Ptgfr-KO mice under DD. In the wild-type mouse, the plasma prostaglandin F 2α (PGF 2α ) levels showed a circadian rhythm under a 12 h cycle of light-dark conditions. In addition, in vitro experiments showed that the addition of PTGFR agonists altered the amplitude of Per2 ::luc activity, and this alteration differed with the timing of the agonist addition. These results lead us to hypothesize that the plasma rhythm of PGF 2α is important for driving clock genes, thus suggesting the involvement of PGF 2α - and Ptgfr -targeting drugs in the biological clock cycle.