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The effect of sex steroids on uterine contractions and histology in acyclic rats


                                                     Fedor Filipović
                                Center for talented youth Belgrade II, Belgrade, fedorf98@gmail.com



          Introduction                                          In the control adult rats, the luminal epithelium consisting
                                                                of high cylindrical cells and endometrial glands were well
          The  ovarian  hormones  cause  cyclic  changes  in  cell   developed. In acyclic control rats the epithelial cell height
          morphology and histology of the female genital tract (1).   decreased when compared with adult. The uteri of acyclic
          The effects of estradiol and progesterone on the contractile   rats  treated  with  EE  were  more  hyperemic  with  higher
          activity of isolated rat uterus, has already been studied (2),   epithelium than in the acyclic control animals. The uterine
          but  the  effect  of  these  hormone  s  on  uterine  smooth   histology of P4 treated acyclic rats were similar to acyclic
          muscles  of  acyclic  comparing  to  adult  rats  are  still   control group.
          unknown.
          In  menopausl  women,  estrogen  replacement  therapy
          increases  the  risk  of  endometrial  cancer  (3).  The  aim  of
          this  study  was  to  investigate  the  effect  of  sex  hormone
          treatment on acyclic rats uterus.

          Materials and methods

          Acyclic  female  Wistar  rats  were  treated  with  ethinyl
          estradiol (EE) or progesterone (P4) for 4 weeks. The third
          group  of  acyclic  rats  and  fourth  adult  group  served  as
          controls. The uterine horns from the control groups were
          used for ex vivo testing of the contractions in organ bath.
          After an equilibration period,  when uteri achieved  stable
                      +
                            2+
          contractions (K  or Ca  ion-induced), myometrial tension
          was  recorded  after  the  addition  of  increasing
          concentrations of EE or P4.
          Part  of  the  uterine  horns  from  the  controls  and  in  vivo
          treated rats were used for histological analysis. The tissues
          were  fixed,  routinely  processed,  embedded  in  paraplast
          and  sectioned  transversely.  Section  were  stained  by  the
          hematoxylin and eosin (H&E) and visualized under a light   Figure  2.  Transversal  sections  of  the  rats  uteri.  Light
          microscope.                                           microscopy, H&E staining.

          Results and discussion
                                                                Conclusion
          Aplication of EE and P4 caused dose-dependent relaxation
          of  both  KCl  and  CaCl 2   stimulated  uteri.  There  are  no   Estradiol and progesterone causes dose-dependent relaxing
          differences between relaxation effect of P4, in the presence   effect on uterine smooth muscles of aciclyc rats. However,
          of KCl or CaCl 2  in acyclic comparing to adult rats. On the   differences in estradiol mediated relaxation between adult
          other  hand,  EE  has  stronger  relaxing  effect  in  KCl   and acyclic rats may be due to modulation of ion channel
          stimulated  acyclic  rat  uteri  than  in  adults,  while  at  low   during  aging.  Histological  analysis  indicated  that  age-
          concentrations  observed  weaker  effect  in  the  uterus   related  decline  in  sex  hormones  disrupts  the  structure  of
          stimulated with CaCl 2 .                              the  uterine  tissue,  while  subsequent  estradiol  trеаtment
                                                                which  causes  hypertrophic  changes  may  additionally
                                                                contribute to the development of endometrial cancer.



                                                                References

                                                                [1]  Spornitz  UM,  Socin  CD,  dravid  AA.  Anatomical
                                                                Record, (1999), 254: 116-126.
                                                                [2] Aman M, Hirano K, Nishimura J, Nakano H, Kanaide
                                                                H.  British  Journal  of  Pharmacology,  (2005),  146:  425–
                                                                434.
                                                                [3] Ziel HK. Obstet Gynecol, (1982), 60: 509–515.
          Figure 1. Dose-response sigmoid fit curves for EE and P4-
          induced relaxation of the isolated rat uterus
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