PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2008 | 64 | 04B |

Tytuł artykułu

Cholinergic innervation of cystic porcine ovaries

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The aim of the study was to examine the changes in the density of VAChT (marker of acetylcholine present)-, NPY-, VIP-, SOM-, SP- and nNOS-immunoreactive (IR) nerve terminals and co-localization of VAChT with the above-mentioned neurotransmitters after the occurrence of dexamethasone (DXM)-induced ovarian cysts in gilts. DXM administration led to an increase in the density of VAChT/SP-, VAChT/nNOS- and NPY-IR nerve terminals around the cystic walls. In DXM-treated animals an elevated number of VAChT- and SP-IR nerve endings was found close to the tertiary follicles. Moreover, in the gilts receiving DXM the density of NPY-IR nerve endings (that simultaneously co-localized VAChT) was high near the interstitial gland. An increase in the number of VAChT/SP- and VIP-IR nerve fibers around the medullar arteries (A) was observed in cystic ovaries, while the number of VAChT-IR nerve endings near the cortical A was lowered after DXM application. Furthermore, nerve fibers containing VAChT were absent around veins in the whole ovary of DXM-treated animals. After DXM injections, an increase in the number of VAChT/SP- and VAChT/nNOS-IR nerve endings in the cortical, as well as VIP- and nNOS-IR (co-existing with VAChT), nerve terminals in the medullar part of the autonomic ground plexus (GP) was present. However, the administration of DXM led to a drop in the density of SOM-positive nerve endings (also VAChT-IR) in the medullar subdivision of the GP. The present study shows that in the porcine ovaries with DXM induced cysts the pattern of cholinergic innervation, as well as the co-localization of VAChT and NPY, VIP, SOM, SP or nNOS, were changed. Data obtained also suggest that acetylcholine and the above-mentioned neurotransmitters effecting the functioning (steroidogenic activity, blood flow) of the polycystic ovaries may have a significant influence on the course of this pathological status.

Wydawca

-

Rocznik

Tom

64

Numer

04B

Opis fizyczny

p.565-570,fig.,ref.

Twórcy

autor
  • Polish Academy of Sciences, Tuwima 10, 10-747 Olsztyn, Poland
autor
autor

Bibliografia

  • 1.Andreani C. L., Lazzarin N., Pierro E., Lanzone A., Mancuso S.: Somatostatin action on rat ovarian steroidogenesis. Hum. Reprod. 1995, 10, 1968-1973.
  • 2.Arancibia S., Estupina C., Tapia-Arancibia L.: Rapid reduction in somatostatin mRNA expression by hypothalamic neurons induced by dexamethasone. Neuroendocrinology 2000, 11, 3163-3167.
  • 3.Babalola G. O., Shapiro B. H.: Sex steroid changes in porcine cystic ovarian disease. Steroids 1990, 55, 319-324.
  • 4.Balen A. H., Jacobs H. S.: A prospective study comparing unilateral and bilateral laparoscopy ovarian diathermy in women with the polycystic ovary syndrome. Fertil. Sterol. 1994, 62, 921-924.
  • 5.Baranowska B., Chmielowska M., Radzikowska M., Borowiec M., Roguski K., Wasilewska-Dziubinska E.: Effects of neuropeptide Y (NPY), galanin and vasoactive intestinal peptide (VIP) on pituitary hormone release and ovarian steroidogenesis. Neuroendocrinol Lett. 1999, 20, 385-389.
  • 6.Barboni B., Martelli A., Berardinelli P., Russo V., Turriani M., Bernabò N., Lucidia P., Mattioli M.: Ovarian follicle vascularization in fasted pig. Theriogenology 2004, 62, 943-997.
  • 7.Bódis J., Tinneberg H. R., Papenfuss F., Török A., Cledon P., Hanf V., Schwarz H.: Cholinergic stimulation of progesterone and estradiol secretion by human granulosa cells cultured in serum-free medium. Gynecol. Endocrinol. 1993, 7, 83-87.
  • 8.Boryczko Z., Bostedt H., Hoffmann B.: Comparison of the hormonal and chemical composition of the fluid from bovine ovarian follicles and cysts. Reprod. Dom. Anim. 1995, 30, 36-38.
  • 9.Calder M. D., Manikkam M., Salfen B. E., Youngquist R. S., Lubahn D. B., Lamberson W. R., Garverick H. A.: Dominant bovine ovarian follicular cysts express increased levels of messenger RNAs for luteinizing hormone receptor and 3 beta-hydroxysteroid dehydrogenase delta (4), delta (5) isomerase compared to normal dominant follicles. Biol. Reprod. 2001, 65, 471-476.
  • 10.Donesky B. W., Adashi E. Y.: Surgically induced ovulation in the polycystic ovary syndrome: wedge resection revisited in the age of laparoscopy. Fertil. Steril. 1995, 63, 439-463.
  • 11.Dorfman M., Arancibia S., Fiedler J. L., Lara H. E.: Chronic intermittent cold stress activates ovarian sympathetic nerves and modifies ovarian follicular development in the rat. Biol. Reprod. 2003, 68, 2038-2043.
  • 12.Dynarowicz I., Dziegielewski M.: The role of the cholinergic system in the regulation of blood flow through the reproductive organs of swine during the estrous cycle. Pol. Arch. Vet. 1987, 27, 69-83.
  • 13.Dzienis A., Majewski M., Wojtkiewicz J., Jana B.: Changes in density of sympathetic nerve terminals and steroidogenic activity of porcine ovaries after dexamethasone-induced polycystic ovarian syndrome. Pol. J. Vet. Sci. 2004, 7, 37-39.
  • 14.Dzienis A., Majewski M., Wojtkiewicz J., Piskuła M., Jana B.: Adrenergic innervation and steroidogenic activity of cystic porcine ovaries. Rocz. Akademii Medycznej w Białymstoku 2004, 49, 114-116.
  • 15.Frautschy S. A., Liptrap R. M.: Anovulation and plasma hormone concentrations after administration of dexamethasone during the middle of the luteal phase in sows undergoing estrous cycles. Am. J. Vet. Res. 1988, 49, 1270-1275.
  • 16.Hong D., Byers M. R., Oswald R. J.: Dexamethasone treatment reduces sensory neuropeptides and nerve sprouting reactions in injured teeth. Pain 1993, 55, 171-181.
  • 17.Jana B., Dzienis A., Rogozińska A., Piskuła M., Jedlinska-Krakowska M., Wojtkiewicz J., Majewski M.: Dexamethasone-induced changes in sympathetic innervation of porcine ovaries and in their steroidogenic activity. J. Reprod. Dev. 2005, 6, 715-725.
  • 18.Jorgensen J. C., Kannisto P., Liedberg F., Ottesen B., Owman C., Schmidt G.: The influence of neuropeptide Y and norepinephrine on ovulation in the rat ovary. Peptides 1991, 12, 975-982.
  • 19.Lakomy M.: Unerwienie adrenergiczne i cholinergiczne narządów układu rozrodczego samiczego świni w różnych okresach cyklu jajnikowego, ciąży i laktacji. Zesz. Prob. Post. Nauk Roln. 1987, 339, 89-104.
  • 20.Lara H. E., Ferruz J. L., Luza S., Bustamante D. A., Borges Y., Ojeda S. R.: Activation of ovarian sympathetic nerves in polycystic ovary syndrome. Endocrinology 1993, 133, 2690-2695.
  • 21.Majewski M.: Afferentne i efferentne unerwienie jajnika świni - źródła pochodzenia i kodowanie chemiczne. Praca hab., Wyd. ART, Olsztyn 1997.
  • 22.Majewski M., Heym C.: The origin of ovarian neuropeptide Y (NPY)-immunoreactive nerve fibres from the inferior mesenteric ganglion in the pig. Cell Tissue Res. 1991, 266, 591-596.
  • 23.Markiewicz W., Jaroszewski J. J., Bossowska A., Majewski M.: NPY: its occurrence and relevance in the female reproductive system. Folia Histochem. 2003, 41, 183-192.
  • 24.Masuda M., Kubota T., Aso T.: Effects of nitric oxide on steroidogenesis in porcine granulose cells during different stages of follicular development. Eur. J. Endocrinol. 2001, 3, 303-308.
  • 25.Nakamura Y.: Treatment of polycystic ovary syndrome: an overview. Horm. Res. 1990, 33, 31.
  • 26.Ogasa A., Domeki I., Itoh S., Tsutsui T., Kawakami E.: The formation of cystic ovarian follicles in the sows after treatment with ACTH. Jap. J. Zootech. Sci. 1988, 59, 1004-1012.
  • 27.Paredes A., Galvez A., Leyton V., Aravena G., Fiedler J. L., Bustamante D., Lara H. E.: Stress promotes development of ovarian cysts in rats: the possible role of sympathetic nerve activation. Endocrine 1998, 8, 309-315.
  • 28.Parra C., Fiedler J. L., Luna S. L., Greiner M., Padmanabhan V., Lara H. E.: Participation of vasoactive intestinal polypeptide in ovarian steroids production during the rat estrous cycle and in the development of estradiol valerate-induced polycystic ovary. Reproduction 2007, 133, 147-154.
  • 29.Pitzel L., Jarry H., Wuttke W.: Effects of substance-P and Neuropeptide-Y on in vitro steroid release by porcine granulosa and luteal cells. Endocrinology 1991, 129, 1059-1065.
  • 30.Ryan P. L., Raeside J. I.: Cystic ovarian degeneration in pigs: a review. Second of two parts. Irih Vet. J. 1991, 44, 27-36.
  • 31.Stones R. W., Loesch A., Beard R. W., Burnstock G.: Substance P: endothelial localization and pharmacology in the human ovarian vein. Obstet. Gynecol. 1995, 85, 273-278.
  • 32.Trzeciak W. H., Ahmed C. E., Simpson E. R., Ojeda S. R.: Vasoactive intestinal peptide induces the synthesis of the cholesterol side-chain cleavage enzyme complex in cultured rat ovarian granulosa cells. Proc. Natl. Acad. Sci. 1986, 83, 7490-7494.
  • 33.Viveiros M. M., Liptrap R. M.: Altered ovarian follicle function in ACTH-treated gilts. Anim. Reprod. Sci. 1995, 40, 107-119.
  • 34.Wulff C., Wilson H., Wiegand S. J., Rudge J. S., Fraser H. M.: Prevention of thecal angiogenesis, antral follicular growth, and ovulation in the primate by treatment with vascular endothelial growth factor trap R1R2. Endocrinology 2002, 143, 2797-2807.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-article-4526b57f-7816-426d-9b34-d852b4b73190
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.