Theriogenology
Volume 73, Issue 2 , Pages 215-224 , 15 January 2010

The influence of steroids on vascular tension of isolated superficial veins of the nose and face during the estrous cycle of gilts

  • W.J. Grzegorzewski

      Affiliations

    • Department of Local Physiological Regulation, Institute of Animal Reproduction and Food Research of the Polish Academy of Sciences, Olsztyn, Poland
    • Corresponding Author InformationCorresponding author. Tel.: +48 895393125; fax: +48 895357421.
  • ,
  • J. Chłopek

      Affiliations

    • Department of Local Physiological Regulation, Institute of Animal Reproduction and Food Research of the Polish Academy of Sciences, Olsztyn, Poland
  • ,
  • A. Tabęcka-Łonczyńska

      Affiliations

    • Department of Animal Physiology and Reproduction. University of Rzeszów, Rzeszów, Poland
  • ,
  • S. Stefańczyk-Krzymowska

      Affiliations

    • Department of Local Physiological Regulation, Institute of Animal Reproduction and Food Research of the Polish Academy of Sciences, Olsztyn, Poland

Received 18 February 2009 ,Revised 11 September 2009 ,Accepted 11 September 2009.

References 

  1. Simoens P, Lauwers H, De Geest JP, De Schaepdrijver L. Functional morphology of the cranial retia mirabilia in the domestic mammals. Schweiz Arch Tierheilk. 1987;129:295–307
  2. Baker MA, Hayward JN. The influence of the nasal mucosa and the carotid rete upon hypothalamic temperature in sheep. J Physiol (Lond). 1968;198:561–579
  3. Cabanac M, Caputa M. Natural selective cooling of the human brain: evidence of its occurrence and magnitude. J. Physiol. 1979;286:255–264
  4. Mitchell D, Maloney SK, Laburn HP, Knight MH, Kuhnen G, Jessen C. Activity, blood temperature and brain temperature of free-ranging springbok. J Comp Physiol B. 1997;167:335–343
  5. Fuller A, Maloney SK, Kamerman PR, Mitchell D. Absence of selective brain cooling in free-ranging zebras in their natural habitat. Exp Physiol. 2000;85:209–217
  6. Krzymowski T, Skipor J, Grzegorzewski W. Cavernous sinus and carotid rete of sheep and sows as a possible place for counter current exchange of some neuropeptides and steroid hormones. Anim Reprod Sci. 1992;29:225–240
  7. Grzegorzewski W, Skipor J, Wąsowska B, Krzymowski T. Counter current transfer of oxytocin from the venous blood of the perihypophyseal cavernous sinus to the arterial blood of carotid rete supplying the hypophysis and brain depends on the phase of the estrous cycle in pigs. Biol Reprod. 1995;52:139–144
  8. Grzegorzewski W, Skipor J, Wąsowska B, Krzymowski T. Counter current transfer of 125J-LH-RH in the perihypophyseal cavernous sinus-carotid rete vascular complex, demonstrated on isolated pig heads perfused with autologous blood. Dom Anim Endocrinol. 1997;14:149–160
  9. Skipor J, Bao S, Grzegorzewski W, Wąsowska B, Rao ChV. The inhibitory effect of hCG on counter current transfer of GnRH and the presence of LH/hCG receptors in the perihypopheseal cavernous sinus-carotid rete vascular complex of ewes. Theriogenology. 1999;51:899–910
  10. Skipor J, Grzegorzewski W, Wąsowska B, Krzymowski T. Counter current transfer of β- endorphin in the perihypophyseal cavernous sinus-carotid rete complex of sheep. Exp Clin Endocrinol Diabetes. 1997;105:308–313
  11. Skipor J, Wąsowska B, Grzegorzewski W, Zezula-Szpyra A, Stefańczyk-Krzymowska S, Thiery JC. Transfer of dopamine by counter current mechanism in ewe changes with endocrine stage. Biog Amine. 2001;16:431–445
  12. Stefańczyk-Krzymowska S, Krzymowski T, Grzegorzewski W, Wąsowska B, Skipor J. Humoral pathway for local transfer of the priming pheromone androstenol from the nasal cavity to the brain and hypophysis in anaesthetized gilts. Exp Physiol. 2000;85:801–809
  13. Krzymowski T, Grzegorzewski W, Stefańczyk-Krzymowska S, Skipor J, Wąsowska B. Humoral pathway for transfer of the boar pheromone, androstenol, from the nasal mucosa to the brain and hypophysis of gilts. Theriogenology. 1999;52:1225–1240
  14. Krzymowski T, Stefańczyk-Krzymowska S, Grzegorzewski W, Skipor J, Wąsowska B. A possible humoral pathway for the priming action of the male pheromone androstenol on female pigs. In:  Marchlewska-Koj A,  Lepri JJ,  Müller-Schwarze D editor. Chemical Signals in Vertebrates 9. Kluwer Academic/Plenum Publishers; 2001;p. 117–123
  15. Stefańczyk-Krzymowska S, Krzymowski T, Wąsowska B, Jana B, Słomiński J. Intramuscular injections of male pheromone 5α-androstenol change the secretory ovarian function in gilts during sexual maturation. Reprod Biol. 2003;3:241–257
  16. Stefańczyk-Krzymowska S, Wąsowska B, Jana B. Boar pheromone androstenol may affect the ovarian morphology in cycling gilts by humoral pathway. Folia Histochem Cytobiol. 2002;40:155–156
  17. Stefańczyk-Krzymowska S, Wąsowska B, Skipor J. The effect of intramuscular injections of boar pheromone 5α-androstenol on the hormonal regulation of the estrous cycle in hypoosmatic gilts. Pol J Vet Sci. 2005;8:85–91
  18. Zezula-Szpyra A, Grzegorzewski W. Morphology of the dorsal nasal. frontal and facial veins in adult gilts. Folia Morphol. 2000;59:179–191
  19. Magilton JH, Swift CS. Response of veins draining the nose to alar-fold temperature changes in dog. J Appl Physiol. 1969;27:18–20
  20. Mitchell J, Thomalla L, Mitchell G. Histological studies of the dorsal nasal, angularis oculi and facial veins of sheep (ovis aries). J Morphol. 1998;237:275–281
  21. Grzegorzewski W. The influence of boar pheromones on the vasoreactivity of the facial superficial veins in the ovariectomized and estradiol-treated pubertal gilts. Pol J Vet Sci. 2006;4:219–225
  22. Grzegorzewski WJ. The influence of male pheromones on the contractile reactivity of the isolated superficial veins of the nose and face during the estrous cycle in gilts. Pol J Vet Sci. 2005;8:57–64
  23. Grzegorzewski WJ. The influence of boar pheromones on the contractile reactivity of the isoloated superficial veins of the nose and face in ovariectomized prepubertal gilts and in gilts during sexual maturation. Pol J Vet Sci. 2006;9:127–133
  24. White RE. Estrogen and vascular function. Vasc Pharmacol. 2002;38:73–80
  25. Brenner RM, Slayden OvD. Steroid receptors in blood vessels of the rhesus macaque endometrium: a review. Arch Histol Cytol. 2004;5:411–416
  26. Chang K, Zhang L. Steroid hormones and uterine vascular adaptation to pregnancy. Reprod Sci. 2008;4:336–348
  27. Nechmad A, Merin G, Schwalb H, Shimon Dov V, Borman JB, Milgalter E, et al. Estrogen induces nitric oxide-mediated vasodilation of human mammary arteries in vitro. Biol Chem. 1998;6:460–466
  28. Sarrel PM. The differential effects of oestrogens and progestins on vascular tone. Hum Reprod Update. 1999;3:205–209
  29. Minshall RD, Pavcnik D, Browne DL, Hermsmeyer K. Nongenomic vasodilator action of progesterone on primate coronary arteries. J Appl Physiol. 2002;92:701–708
  30. Simoncini T, Genazzini AR. Non-genomic actions of sex steroid hormones. Eur J Endocrinol. 2003;148:281–292
  31. Bracamonte MP, Jayachandran M, Rud KS, Miller VM. Acute effects of 17β-estradiol on femoral veins from adult gonadally intact and ovariectomized female pigs. Am J Physiol Circ Physiol. 2002;283:H2389–H2396
  32. Hodges YK, Tung L, Yan XD, Graham JD, Horwitz KB, Horwitz LD. Estrogen receptors α and β. Prevalence of estrogen receptor β mRNA in human vascular smooth muscle and transcriptional effects. Circulation. 2000;101:1792–1798
  33. Yue P, Chatterjee K, Beale C, Poole-Wilson PA, Collins P. Testosterone relaxes rabbit coronary arteries and aorta. Circulation. 1995;91:1154–1160
  34. Teoh H, Quan A, Leung SS, Man RK. Differential effects of 17β-estradiol and testosterone on the contractile responses of porcine coronary arteries. Br J Pharmacol. 2000;129:1301–1308
  35. Jones RD, Jones TH, Channer KS. The influence of testosterone upon vascular reactivity. Eur J Endocrinol. 2004;151:29–37
  36. Reynolds LP, Ford SP. Contractility of the ovarian vascular bed during the oestrous cycle and early pregnancy in gilts. J Reprod Fert. 1984;71:65–71
  37. Stice SL, Ford SP, Rosazza JP, Van Orden DE. Interaction of 4-hydroxylated estradiol and potential-sensitive Ca2+ channels in altering uterine blood flow during the estrous cycle and early pregnancy in gilts. Biol Reprod. 1987;36:369–375
  38. Ford SP, Reynolds LP, Farley DB, Bhatnagar RK, Van Orden DE. Interaction of ovarian steroids and periarterial α1-adrenergic receptors in altering uterine blood flow during the estrous cycle of gilts. Am J Obstet Gynecol. 1984;150:480–484
  39. Li X, Geary GG, Gonzales RJ, Krause DN, Duckles SP. Effect of estrogen on cerebrovascular prostaglandins is amplified in mice with dysfunctional NOS. Am J Physiol Heart Circ Physiol. 2004;287:H588–H594
  40. Byers MJ, Zangl A, Phernetton TM, Lopez G, Chen DB, Magness RR. Endothelial vasodilator production by ovine uterine and systemic arteries: ovarian steroid and pregnancy control of ERα and ERβ levels. J Physiol. 2005;565:85–99
  41. Huang A, Wu Y, Sun D, Koller A, Kaley G. Effect of estrogen on flow-induced dilation in NO deficiency: role of prostaglandins and EDHF. J Appl Physiol. 2001;91:2561–2566
  42. Haas E, Meyer MR, Schurr U, Bhattacharya I, Minotti R, Nguyen HH, et al. Differential effects of 17β-estradiol on function and expression of estrogen receptor α. estrogen receptor β and GPR30 in arteries and veins of patients with artherosclerosis. Hypertension. 2007;49:1358–1363
  43. Eid AH, Maiti K, Mitra S, Chotani MA, Flavahan S, Bailey SR, et al. Estrogen increases smooth muscle expresion of α2C-adrenoceptors and cold-induced constriction of cutaneous arteries. Am J Physiol Circ Physiol. 2007;293:H1955–H1961
  44. Veille JC, Li P, Eisenach JC, Massmann AG, Figueroa JP. Effects of estrogen on nitric oxide biosynthesis and vasorelaxant activity in sheep uterine and renal arteries in vitro. Am J Obstet Gynecol. 1996;3:1043–1049
  45. Fu XD, Simoncini T. Non-genomic sex steroid actions in the vascular system. Semin Reprod Med. 2007;3:178–186
  46. Valverde MA, Rojas P, Amigo J, Cosmelli D, Orio P, Bahamonde MI, et al. Acute activation of Maxi-K channels (hSlo) by estradiol binding to the beta subunit. Science. 1999;285:1929–1931
  47. Beale C, Rosano GMC, Sontag P, Collins P. Effect of testosterone on coronary blood flow velocity to acetylcholine in men with coronary artery disease. J Am Coll Cardiol. 1997;29(suppl.):373A;(Abstract)
  48. Fu XD, Simoncini T. Extra-nuclear signaling of estrogen receptors. IUBMB Life. 2008;8:502–510
  49. Stefańczyk-Krzymowska S, Wąsowska B, Chłopek J, Grzegorzewski W. Retrograde transfer of steroid hormones to the ovary in luteal and follicular phases of porcine oestrous cycle in vivo. Exp Physiol. 2004;89:140–144
  50. Deenadayalu VP, White RE, Stallone JN, Gao X, Garcia AJ. Testosterone relaxes coronary arteries by opening the large-conductance. calcium-activated potassium channel. Am J Physiol Heart Circ Physiol. 2001;281:H1720–H1727
  51. Pardridge WM. In:  Conn PM,  Goodman HM editor. Handbook of Physiology: The Endocrine System. Oxford University Press; 1998;p. 335–382

PII: S0093-691X(09)00403-8

doi: 10.1016/j.theriogenology.2009.09.002

Theriogenology
Volume 73, Issue 2 , Pages 215-224 , 15 January 2010