BMC Veterinary Research | |
No up-regulation of the phosphatidylethanolamine N-methyltransferase pathway and choline production by sex hormones in cats | |
Jan Rothuizen1  Isabelle Jeusette3  Anne Kummeling1  Maidina Tuohetahuntila2  Joris H. Robben1  Robert P. Favier1  Arie B. Vaandrager2  Chiara Valtolina1  | |
[1] Department of Clinical Sciences of Companion Animals, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 108, Utrecht, 3584 CM, The Netherlands;Department of Biochemistry and Cell Biology, Faculty of Veterinary Medicine and Institute of Biomembranes, Utrecht University, Yalelaan 2, Utrecht, 3584 CM, The Netherlands;Research and Development, Affinity Petcare, Pl. Xavier Cugat, 2 Edificio D, 3ª, Planta, 08174 St. Cugat del Vallès, Barcelona, Spain | |
关键词: Oestrogen; PEMT; Choline; Hepatic lipidosis; Cats; | |
Others : 1233999 DOI : 10.1186/s12917-015-0591-6 |
|
received in 2015-04-14, accepted in 2015-11-02, 发布年份 2015 | |
![]() |
【 摘 要 】
Background
Feline hepatic lipidosis (FHL) is a common cholestatic disease affecting cats of any breed, age and sex. Both choline deficiency and low hepatic phosphatidylethanolamine N-methyltransferase (PEMT) activity are associated with hepatic lipidosis (HL) in humans, mice and rats. The PEMT expression is known to be upregulated by oestrogens, protecting the females in these species from the development of HL when exposed to choline deficient diets. The aim of the present study was to evaluate the influence of sex hormones on choline synthesis via the PEMT pathway in healthy male and female cats before and after spaying/neutering, when fed a diet with recommended dietary choline content.
Results
From six female and six male cats PEMT activity was assayed directly in liver biopsies taken before and after spaying/neutering, and assessed indirectly by analyses of PEMT–specific hepatic phosphatidylcholine (PC) species and plasma choline levels. Hepatic PEMT activity did not differ between intact female and male cats and no changes upon spaying/neutering were observed. Likewise, no significant differences in liver PC content and PEMT-specific polyunsaturated PC species were found between the sexes and before or after spaying/neutering.
Conclusion
These results suggest that choline synthesis in cats differs from what is observed in humans, mice and rats. The lack of evident influence of sex hormones on the PEMT pathway makes it unlikely that spaying/neutering predisposes cats for HL by causing PC deficiency as suggested in other species.
【 授权许可】
2015 Valtolina et al.
【 预 览 】
Files | Size | Format | View |
---|---|---|---|
20151125032516554.pdf | 414KB | ![]() |
【 参考文献 】
- [1]Armstrong PJ, Blanchard G. Hepatic lipidosis in cats. Vet Clin North Am Small Anim Pract. 2009; 39(3):599-616.
- [2]Center SA. Feline hepatic lipidosis. Vet Clin North Am Small Anim Pract. 2005; 35(1):225-69.
- [3]Center SA, Crawford MA, Guida L, Erb HN, King J. A retrospective study of 77 cats with severe hepatic lipidosis: 1975–1990. J Vet Intern Med. 1993; 7(6):349-59.
- [4]Pazak HE, Bartges JW, Cornelius LC, Scott MA, Gross K, Huber TL. Characterization of serum lipoprotein profiles of healthy, adult cats and idiopathic feline hepatic lipidosis patients. J Nutr. 1998; 128(12 Suppl):2747S-50.
- [5]DeLong CJ, Shen YJ, Thomas MJ, Cui Z. Molecular distinction of phosphatidylcholine synthesis between the CDP-choline pathway and phosphatidylethanolamine methylation pathway. J Biol Chem. 1999; 274(42):29683-8.
- [6]Vance DE. Phospholipid biosynthesis in eukaryotes. In: Biochemistry of Lipids, Lipoproteins and Membranes. 5th ed. Vance DE, Vance JE, editors. Elsevier, Amsterdam; 2002: p.205-32.
- [7]Vance DE, Ridgway ND. The methylation of phosphatidylethanolamine. Prog Lipid Res. 1988; 49:1187-94.
- [8]Li Z, Vance DE. Phosphatidylcholine and choline homeostasis. J Lipid Res. 2008; 49(6):1187-94.
- [9]da Costa KA, Sanders LM, Fischer LM, Zeisel SH. Docosahexaenoic acid in plasma phosphatidylcholine may be a potential marker for in vivo phosphatidylethanolamine N-methyltransferase activity in humans. Am J Clin Nutr. 2011; 93(5):968-74.
- [10]Pani P, Porcu M, Columbano A, Dessi S, Ledda GM, Diaz G. Differential effects of choline administration on liver microsomes of female and male rats. Exp Mol Pathol. 1978; 28(2):154-62.
- [11]Noga AA, Vance DE. A gender-specific role for phosphatidylethanolamine N-methyltransferase-derived phosphatidylcholine in the regulation of plasma high density and very low density lipoproteins in mice. J Biol Chem. 2003; 278(24):21851-9.
- [12]Zeisel SH. Choline: an essential nutrient for humans. Nutrition. 2000; 16(7–8):669-71.
- [13]Da Silva AC, Guerios SMF, Monsao SR. The domestic cat as a laboratory animal for experimental nutrition studies. VI. Choline deficiency. J Nutr. 1959; 67(4):537-47.
- [14]Anderson PA, Baker DH, Sherry PA, Corbin JE. Choline-methionine interrelationship in feline nutrition. J Anim Sci. 1979; 49(2):522-7.
- [15]Schaeffer MC, Rogers QR, Morris JG. Methionine requirement of the growing kitten, in the absence of dietary cystine. J Nutr. 1982; 112(5):962-71.
- [16]Verbrugghe A, Bakovic M. Peculiarities of one-carbon metabolism in the strict carnivorous cat and the role in feline hepatic lipidosis. Nutrients. 2013; 5(7):2811-35.
- [17]Li Z, Agellon LB, Vance DE. Phosphatidylcholine homeostasis and liver failure. J Biol Chem. 2005; 280(45):37798-802.
- [18]Vance JE, Vance DE. The role of phosphatidylcholine biosynthesis in the secretion of lipoproteins from hepatocytes. Can J Biochem Cell Biol. 1985; 63(8):870-81.
- [19]Yao ZM, Vance DE. The active synthesis of phosphatidylcholine is required for very low density lipoprotein secretion from rat hepatocytes. J Biol Chem. 1988; 263(6):2998-3004.
- [20]Yao ZM, Vance DE. Head group specificity in the requirement of phosphatidylcholine biosynthesis for very low density lipoprotein secretion from cultured hepatocytes. J Biol Chem. 1989; 264(19):11373-80.
- [21]Yao ZM, Vance DE. Reduction in VLDL, but not HDL, in plasma of rats deficient in choline. Biochem Cell Biol. 1990; 68(2):552-8.
- [22]Buchman AL, Dubin MD, Moukarzel AA, Jenden DJ, Roch M, Rice KM, Gornbein J, Ament ME. Choline deficiency: a cause of hepatic steatosis during parenteral nutrition that can be reversed with intravenous choline supplementation. Hepatology. 1995; 22(5):1399-403.
- [23]Fischer LM, da Costa KA, Kwock L, Stewart PW, Lu TS, Stabler SP, Allen RH, Zeisel SH. Sex and menopausal status influence human dietary requirements for the nutrient choline. Am J Clin Nutr. 2007; 85(5):1275-85.
- [24]Resseguie M, Song J, Niculescu MD, da Costa KA, Randall TA, Zeisel SH. Phosphatidylethanolamine N-methyltransferase (PEMT) gene expression is induced by estrogen in human and mouse primary hepatocytes. FASEB J. 2007; 21(10):2622-32.
- [25]Young DL. Estradiol- and testosterone-induced alterations in phosphatidylcholine and triglyceride synthesis in hepatic endoplasmic reticulum. J Lipid Res. 1971; 12(5):590-5.
- [26]Nutrient requirements of dogs and cats. 2006.
- [27]Gardiner JE, Paton WD. The control of the plasma choline concentration in the cat. J Physiol. 1972; 227(1):71-86.
- [28]Dieleman SJ, Bevers MM. Effects of monoclonal antibody against PMSG administered shortly after the preovulatory LH surge on time and number of ovulations in PMSG/PG-treated cows. J Reprod Fertil. 1987; 81(2):533-42.
- [29]van Haaften B, Bevers MM, van den Brom WE, Okkens AC, van Sluijs FJ, Willemse AH, Dieleman SJ. Increasing sensitivity of the pituitary to GnRH from early to late anoestrus in the beagle bitch. J Reprod Fertil. 1994; 101(1):221-5.
- [30]Buijtels JJ, Beijerink NJ, Kooistra HS, Dieleman SJ, Okkens AC. Effects of gonadotrophin releasing hormone administration on the pituitary-ovarian axis in anoestrous vs ovariectomized bitches. Reprod Domest Anim. 2006; 41(6):555-61.
- [31]Ridgway ND, Vance DE. Phosphatidylethanolamine N-methyltransferase from rat liver. Methods Enzymol. 1992; 209:366-74.
- [32]Testerink N, Ajat M, Houweling M, Brouwers JF, Pully VV, van Manen HJ, Otto C, Helms JB, Vaandrager AB. Replacement of retinyl esters by polyunsaturated triacylglycerol species in lipid droplets of hepatic stellate cells during activation. PLoS One. 2012; 7(4):e34945.
- [33]Bleijerveld OB, Brouwers JF, Vaandrager AB, Helms JB, Houweling M. The CDP-ethanolamine pathway and phosphatidylserine decarboxylation generate different phosphatidylethanolamine molecular species. J Biol Chem. 2007; 282(39):28362-72.