Korean J Obstet Gynecol.  2010 Apr;53(4):354-359. 10.5468/kjog.2010.53.4.354.

The effect of pomegranate on postmenopausal syndrome in ovariectomized rats

Affiliations
  • 1Department of Obstetrics and Gynecology, Korea University Medical Center, Korea University College of Medicine, Gwangju, Korea. tkim@kumc.or.kr
  • 2Department of Veterinary Surgery, College of Veterinary Medicine, Chonnam National University, Seoul, Korea.

Abstract


OBJECTIVE
To determine whether or not pomegranate extract can affect postmenopausal syndrome in ovariectomized rats.
METHODS
Seventy-nine female Sprague-Dawley rats were used: A, no intervention; B, sham operation and distilled water; C, ovariectomy and distilled water; D, ovariectomy and 10% dilute pomegranate; E, ovariectomy and 20% pomegranate; and F, ovariectomy and 40% pomegranate. The study samples were obtained 4 weeks later. The following parameters were investigated for analyses: the thickness of urogenital epithelium, tail skin temperature, serum levels of sex hormones, lipid profile, homocysteine, and thiobarbituric acid reactive substances.
RESULTS
20% pomegranate had a transient thickening effect of bladder epithelial layer. There was an intermittent lowering effect of tail skin temperature of pomegranate extract, however, it was not consistent. There were lowering effect in serum homocysteine and elevating effect in serum high density lipoprotein-cholesterol. Pomegranate did not reverse post-ovariectomy reduced sex hormone levels.
CONCLUSION
Pomegranate extract showed a tendency to reverse ovariectomy-related urothelial changes. Also pomegranate had a serum homocysteine-lowering effect.

Keyword

Pomegranate; Postmenopausal syndrome

MeSH Terms

Animals
Epithelium
Female
Gonadal Steroid Hormones
Homocysteine
Humans
Ovariectomy
Punicaceae
Rats
Rats, Sprague-Dawley
Salicylamides
Skin Temperature
Tail
Thiobarbiturates
Thiobarbituric Acid Reactive Substances
Urinary Bladder
Gonadal Steroid Hormones
Homocysteine
Salicylamides
Thiobarbiturates
Thiobarbituric Acid Reactive Substances

Figure

  • Fig. 1 The change of tail skin temperature. Analysis of variance (ANOVA). A: intact, B: sham operation, C: ovariectomy, D: ovariectomy plus 10% pomegranate, E: ovariectomy plus 20% pomegranate, F: ovariectomy plus 40% pomegranate. *Statistically significant.


Reference

1. Roy S, Caillouette JC, Roy T, Faden JS. Vaginal pH is similar to follicle-stimulating hormone for menopause diagnosis. Am J Obstet Gynecol. 2004. 190:1272–1277.
Article
2. Oldenhave A, Jaszmann LJ, Haspels AA, Everaerd WT. Impact of climacteric on well-being. A survey based on 5213 women 39 to 60 years old. Am J Obstet Gynecol. 1993. 168:772–780.
3. Mittal G, Chandraiah G, Ramarao P, Ravi Kumar MN. Pharmacodynamic evaluation of oral estradiol nanoparticles in estrogen deficient (ovariectomized) high-fat diet induced hyperlipidemic rat model. Pharm Res. 2009. 26:218–223.
Article
4. Bruschi F, Meschia M, Soma M, Perotti D, Paoletti R, Crosignani PG. Lipoprotein (a) and other lipids after oophorectomy and estrogen replacement therapy. Obstet Gynecol. 1996. 88:950–954.
5. Hersh AL, Stefanick ML, Stafford RS. National use of postmenopausal hormone therapy: annual trends and response to recent evidence. JAMA. 2004. 291:47–53.
6. Bukulmez O, Al A, Gurdal H, Yarali H, Ulug B, Gurgan T. Short-term effects of three continuous hormone replacement therapy regimens on platelet tritiated imipramine binding and mood scores: a prospective randomized trial. Fertil Steril. 2001. 75:737–743.
Article
7. Rossouw JE, Anderson GL, Prentice RL, LaCroix AZ, Kooperberg C, Stefanick ML, et al. Risks and benefits of estrogen plus progestin in healthy postmenopausal women: principal results From the Women's Health Initiative randomized controlled trial. JAMA. 2002. 288:321–333.
8. Grady D, Herrington D, Bittner V, Blumenthal R, Davidson M, Hlatky M, et al. Cardiovascular disease outcomes during 6.8 years of hormone therapy: Heart and Estrogen/progestin Replacement Study follow-up (HERS II). JAMA. 2002. 288:49–57.
9. van Elswijk DA, Schobel UP, Lansky EP, Irth H, van der Greef J. Rapid dereplication of estrogenic compounds in pomegranate (Punica granatum) using on-line biochemical detection coupled to mass spectrometry. Phytochemistry. 2004. 65:233–241.
Article
10. Kim ND, Mehta R, Yu W, Neeman I, Livney T, Amichay A, et al. Chemopreventive and adjuvant therapeutic potential of pomegranate (Punica granatum) for human breast cancer. Breast Cancer Res Treat. 2002. 71:203–217.
Article
11. Jurenka JS. Therapeutic applications of pomegranate (Punica granatum L.): a review. Altern Med Rev. 2008. 13:128–144.
12. Shah S, Bell RJ, Davis SR. Homocysteine, estrogen and cognitive decline. Climacteric. 2006. 9:77–87.
Article
13. Notelovitz M. Estrogen therapy in the management of problems associated with urogenital ageing: a simple diagnostic test and the effect of the route of hormone administration. Maturitas. 1995. 22:Suppl. S31–S33.
Article
14. Shanafelt TD, Barton DL, Adjei AA, Loprinzi CL. Pathophysiology and treatment of hot flashes. Mayo Clin Proc. 2002. 77:1207–1218.
Article
15. Basu A, Penugonda K. Pomegranate juice: a heart-healthy fruit juice. Nutr Rev. 2009. 67:49–56.
Article
16. Rosenblat M, Hayek T, Aviram M. Anti-oxidative effects of pomegranate juice (PJ) consumption by diabetic patients on serum and on macrophages. Atherosclerosis. 2006. 187:363–371.
Article
17. Rocha MA, Sartori MG, Girão MJ, De Jesus Simões M, Baracat EC, Rodrigues of. Histomorphometric study of the inferior urinary tract of adult female rats during the interval between castration and hormonal replacement. Clin Exp Obstet Gynecol. 2003. 30:111–116.
18. Herrmann W, Obeid R, Hubner U, Jouma M, Geisel J. Homocysteine in relation to C-reactive protein and low-density lipoprotein cholesterol in assessment of cardiovascular risk. Cell Mol Biol (Noisy-le-grand). 2004. 50:895–901.
19. Ungvari Z, Pacher P, Rischak K, Szollar L, Koller A. Dysfunction of nitric oxide mediation in isolated rat arterioles with methionine diet-induced hyperhomocysteinemia. Arterioscler Thromb Vasc Biol. 1999. 19:1899–1904.
Article
20. van Guldener C, Stehouwer CD. Hyperhomocysteinemia, vascular pathology, and endothelial dysfunction. Semin Thromb Hemost. 2000. 26:281–289.
Article
21. Smolders RG, Sipkema P, Kenemans P, Stehouwer CD, Van Der Mooren MJ. Homocysteine impairs estrogen-induced vasodilation in isolated rat arterioles. Menopause. 2004. 11:98–103.
Article
22. Morris MS, Jacques PF, Selhub J, Rosenberg IH. Total homocysteine and estrogen status indicators in the Third National Health and Nutrition Examination Survey. Am J Epidemiol. 2000. 152:140–148.
Article
23. Christodoulakos GE, Panoulis CP, Lambrinoudaki IV, Dendrinos SG, Rizos DA, Creatsas GC. Effect of hormone replacement therapy and tibolone on serum total homocysteine levels in postmenopausal women. Eur J Obstet Gynecol Reprod Biol. 2004. 112:74–79.
Article
24. Chiantera V, Sarti CD, Fornaro F, Farzati A, De Franciscis P, Sepe E, et al. Long-term effects of oral and transdermal hormone replacement therapy on plasma homocysteine levels. Menopause. 2003. 10:286–291.
Article
25. Miller AL. The methionine-homocysteine cycle and its effects on cognitive diseases. Altern Med Rev. 2003. 8:7–19.
26. Selhub J, Bagley LC, Miller J, Rosenberg IH. B vitamins, homocysteine, and neurocognitive function in the elderly. Am J Clin Nutr. 2000. 71:614S–620S.
Article
27. Freedman RR, Krell W. Reduced thermoregulatory null zone in postmenopausal women with hot flashes. Am J Obstet Gynecol. 1999. 181:66–70.
Article
28. Harris HA, Katzenellenbogen JA, Katzenellenbogen BS. Characterization of the biological roles of the estrogen receptors, ERalpha and ERbeta, in estrogen target tissues in vivo through the use of an ERalpha-selective ligand. Endocrinology. 2002. 143:4172–4177.
29. Okada M, Hayashi N, Kometani M, Nakao K, Inukai T. Influences of ovariectomy and continuous replacement of 17beta-estradiol on the tail skin temperature and behavior in the forced swimming test in rats. Jpn J Pharmacol. 1997. 73:93–96.
30. Bowe J, Li XF, Kinsey-Jones J, Heyerick A, Brain S, Milligan S, et al. The hop phytoestrogen, 8-prenylnaringenin, reverses the ovariectomy-induced rise in skin temperature in an animal model of menopausal hot flushes. J Endocrinol. 2006. 191:399–405.
Article
Full Text Links
  • KJOG
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr