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. 2006 Jan 23;5:2. doi: 10.1186/1476-511X-5-2

Selective remodeling of cardiolipin fatty acids in the aged rat heart

Ho-Joo Lee 1, Jana Mayette 1, Stanley I Rapoport 1, Richard P Bazinet 1,✉
PMCID: PMC1402292  PMID: 16430781

Abstract

Background

The heart is rich in cardiolipin, a phospholipid acylated in four sites, predominately with linoleic acid. Whether or not aging alters the composition of cardiolipin acyl chains is controversial. We therefore measured the fatty acid concentration of cardiolipin in hearts of 4, 12 and 24 month old rats that consumed one diet, adequate in fatty acids for the duration of their life.

Results

The concentration (nmol/g) of linoleic acid was decreased in 24 month old rats (3965 ± 617, mean ± SD) vs 4 month old rats (5525 ± 656), while the concentrations of arachidonic and docosahexaenoic acid were increased in 24 month old rats (79 ± 9 vs 178 ± 27 and 104 ± 16 vs 307 ± 68 for arachidonic and docosahexaenoic acids, 4 months vs 24 months, respectively). Similar changes were not observed in ethanolamine glycerophospholipids or plasma unesterified fatty acids, suggesting specificity of these effects to cardiolipin.

Conclusion

These results demonstrate that cardiolipin remodeling occurs with aging, specifically an increase in highly unsaturated fatty acids.

Background

Cardiolipin (1'- [1,2-diacyl-sn-glycero-3-phosphoryl]-3'- [1",2"-diacyl-sn-glycero-3"-phosphoryl]-sn-glycerol; 1,3-diphosphatidylglycerol) is a phospholipid found in particularly high concentrations in the heart. In mammalian cells, it is localized to the inner mitochondrial membrane [1] and is known for its unique and specific acyl structure. Cardiolipin, unlike other mammalian phospholipids, contains 4 stereospecifically numbered acyl groups. Heart cardiolipin is predominately acylated with linoleic acid [2]. The acyl specificity of cardiolipin is believed to occur via remodeling, as the enzymes responsible for its de novo synthesis are not acyl group specific [3,4].

Despite being discovered a relatively long time ago [5], fairly little is known about the function of cardiolipin, especially in mammalian cells. Several excellent reviews have summarized the known biochemistry and functions of cardiolipin which is thought to regulate several mitochondrial proteins [6-9]. It also is known that cardiolipin acyl chains vary greatly by species [10-13] and tissue, and can be modified by diet [14-17]. However, the functional significance of these changes is not known. It is controversial whether the acyl-chain composition of cardiolipin is altered with ageing. Several studies have reported that heart and liver total cardiolipin decreases with age [18-20]. However, studies measuring the fatty acid composition (percent composition) of cardiolipin isolated from aged rat hearts has led to controversial findings, with one study [19] reporting no change in the acyl percent composition and another decreased linoleic and increased arachidonic acid percent compositions [20].

Because of several controversial reports, and of difficulties in interpreting changes in percent composition (a decrease in the concentration of one fatty acid increases the percent composition of other fatty acids), our objective was to evaluate the absolute fatty acid concentration of cardiolipin (nmol/g of tissue) in rat heart as a function of age. By comparing cardiolipin acyl species to those of another major heart phospholipid (ethanolamine glycerophospholipid), and to plasma unesterified fatty acids, we are able to determine if any observed effects are specific to cardiolipin or may be related to substrate availability.

Results

Twenty four and 12 month old rats weighed significantly more than 4 month old rats (396 ± 13, 415 ± 30 and 291 ± 20 grams, for 24, 12 and 4 month old rats, respectively p < 0.01). As well, hearts from 24 and 12 month old rats weighed significantly more than hearts from 4 month old rats (0.91 ± .08, 0.92 ± 0.07 and 0.75 ± 0.06 grams for 24, 12 and 4 month old rats, respectively p < 0.01).

The concentration of linoleic acid was significantly lower (28 %) in the heart of 24 month-old rats compared to 4 month old rats (p < 0.01), while the concentrations of palmitic, arachidonic and docosahexaenoic acids were increased 46 % (p < 0.05), 99 % (p < 0.001) and 195 % (p < 0.001), respectively (Table 1). The concentrations of arachidonic and docosahexaenoic acids were also significantly higher in cardiolipin 12 month old rat hearts, compared to 4 month old rat hearts. Ethanolamine glycerophospholipid linoleic acid concentrations of were 56% lower in hearts of 24 month-old rats compared hearts of 4 month-old rats (p < 0.001). There was no significant difference in other fatty acids within ethanolamine glycerophospholipids between 24 month and 4 month-old rat hearts. The concentration of plasma unesterified stearic acid was significantly lower in 24 month, compared to 4 month old rats (Table 2), but there was no other significant difference in any measured plasma unesterified plasma fatty acids concentration.

Table 1.

Concentration of selected fatty acids in cardiolipin and ethanolamine glycerophospholipids of 4, 12 and 24 month old rat hearts

Cardiolipin Ethanolamine Glycerophospholipids
Fatty Acid 4 Months 12 Months 24 Months 4 Months 12 Months 24 Months
Palmitic acid (16:0) 44 ± 7a 62 ± 15 64 ± 15 * 1166 ± 150 1426 ± 297 1135 ± 129
Stearic acid (18:0) 47 ± 4 49 ± 10 47 ± 14 3943 ± 327 4068 ± 806 3295 ± 373
Oleic acid (18:1n-9) 279 ± 42 291 ± 53 347 ± 57 394 ± 46 372 ± 88 349 ± 30
Linoleic acid (18:2n-6) 5525 ± 656 6025 ± 1094 3965 ± 617 ** 1032 ± 168 864 ± 158 * 459 ± 129 ***
Arachidonic acid (20:4n-6) 79 ± 9 140 ± 54 * 178 ± 27 *** 2625 ± 155 2662 ± 595 2346 ± 260
Docosahexaenoic acid (22:6n-3) 104 ± 16 230 ± 95 * 307 ± 68 *** 3511 ± 279 4436 ± 899 * 3576 ± 326
Σ Of major fatty acids 8374 ± 650 8652 ± 1278 7107 ± 845 * 12672 ± 1032 132829 ± 2796 11161 ± 1002
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a Data are mean ± SD, n = 6 samples per group, nmol/g wet weight *, p < 0.05, **p < 0.01, ***p < 0.001 vs 4 Months.

Table 2.

Plasma concentration of major unesterified fatty acids in 4, 12 and 24 month old rats

Fatty Acid 4 Months (nmol/ml) 12 Months (nmol/ml) 24 Months (nmol/ml)
Palmitic acid (16:0) 450 ± 85 396 ± 142 293 ± 162
Stearic acid (18:0) 130 ± 17 112 ± 26 86 ± 23 *
Oleic acid (18:1n-9) 281 ± 75 291 ± 156 226 ± 148
Linoleic acid (18:2n-6) 366 ± 94 397 ± 231 254 ± 135
Arachidonic acid (20:4n-6) 69 ± 16 73 ± 33 56 ± 18
Docosahexaenoic acid (22:6n-3) 20 ± 7 21 ± 10 16 ± 7
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Data are mean ± SD n = 6 per group. * p < 0.05 vs 4 Months

Discussion

Heart fatty acid concentrations in the current study agree with those previously published[21,22]. The total concentration of cardiolipin has been shown to decrease with age in human epidermal cells [13], and in the liver [19] and heart of the rat [18,20]. However, it is controversial as to whether or not heart cardiolipin is also remodeled (changes its acyl composition) with age. One study reported that aging increased the percent composition of arachidonic acid, while another reported no change in percent composition [18,20]. Assessing fatty acid changes in terms of percent composition is difficult, as a decrease or increase in the concentration of one has the opposite effect on the percent composition of other fatty acids. Here we show for the first time that the absolute concentration of linoleic acid decreases in cardiolipin of the aged rat heart, while although quantitatively less, the absolute concentration of arachidonic and docosahexaenoic acids increases. In the current study, total fatty acids in ethanolamine glycerophospholipids did not change and this is broadly consistent with several other studies reporting no change in heart ethanolamine glycerophospholipids with age [10,19,20]. Because the amount of cardiolipin was shown to decrease with age, it was not surprising to find a decrease in total fatty acid and linoleic acid concentrations. However, our finding that arachidonic acid and docosahexaenoic acid concentrations increased supports the hypothesis that cardiolipin remodeling occurs with ageing. More specifically, this remodeling increases dietary essential highly unsaturated fatty acids [20]. Increased concentrations of arachidonic and docosahexaenoic acid were not observed in the ethanolamine glycerophospholipid class, and thus unlikely reflect their availability. The changes most likely represent changes in cardiolipin acylation/deacylation in heart. Further supporting this idea is that there was no difference in the plasma unesterified fatty acid concentrations of linoleic, arachidonic and docosahexaenoic acid, the major source of heart fatty acids [23]. Increased arachidonic and docosahexaenoic acids in cardiolipin of the aged heart may help to maintain a high unsaturation index in the presence of decreased linoleic acid [20].

The implications of cardiolipin remodeling with age are not known. In patients with systemic lupus erythematosus, cardiolipin acyl groups are believed to form epitopes with antiphospholipid antibodies, and it has been shown that linolenic acid acyl groups have the highest affinity for antiphospholipid antibodies [24]. Thus cardiolipin remodeling with aging may alter cardiolipin's binding to antiphospholipid antibodies, altering the autoimmune response in conditions such as systemic lupus erythematosus. Increased lipid peroxidation is a plausible mechanism by which cardiolipin levels decrease with age. Therefore, increasing the unsaturation of the acyl-side chains would be expected to increase their susceptibility to peroxidation [25]. Furthermore, cardiolipin remodeling can alter the oxygen consumption by the heart and the remodeling observed with aging may contribute to this process [9].

Conclusion

In summary, our results show that cardiolipin remodeling does occur with aging and specifically that the increased concentrations of the nutritionally essential highly unsaturated fatty acids, arachidonic and docosahexaenoic are specific to rat heart cardiolipin as it does not occur in ethanolamine glycerophospholipids. Although several models (dietary, aging) have shown that remodeling of cardiolipin does occur, the functional significance of this effects remains unknown.

Methods

Animals

The study was conducted following the National Institutes of Health Guidelines for the Care and Use of Laboratory Animals (Publication no. 80-23), and was approved by the National Institutes of Child Health and Development Animal Care and Use Committee. Male CDF-344 rats, 4, 12 and 24 months of age were obtained from the National Institutes on Aging colony (Baltimore, MD). The rats were acclimatized for 1 week in an animal facility in which temperature, humidity and light cycle were controlled, and had ad libitum access to food (NIH-31) from weaning until the completion of the study. The NIH-31 diet contains 20.1 % total saturates, 22.5 % total monounsaturates, 47. 9 % linoleic acid, 5.1% α-linolenic acid, 0.02% arachidonic acid and 2.3 % docosahexaenoic acid (see lipid extraction and chromatography section for diet analysis). This diet is adequate in both omega 3 and 6 fatty acids [26].

Rats were removed from food and water for approximately one hour before being anesthetized with sodium pentobarbital and decapitated. We previously showed that microwave fixation is not required to determine the phospholipid concentration of the rat heart [22]. A blood sample was collected from the decapitated animal and the heart was quickly removed, rinsed in ice-cold saline and frozen at -80°C.

Lipid extraction and chromatography

Total lipids were extracted from diet, plasma and heart according the method of Folch [27]. Heptadecaenoic acid (17:0) was added as an internal standard to plasma prior to extraction. The extracts were separated by thin layer chromatography on silica gel plates (Whatman, Clifton, NJ). Ethanolamine glycerophospholipid was separated in chloroform: methanol: H2O: glacial acetic acid (60:50:4:1 by volume) [28] and identified with unlabeled standards in separate lanes. Cardiolipin was separated using acetone and petroleum ether (1:3 by volume). The plate was removed, briefly allowed to dry and rerun using chloroform, methanol and glacial acetic acid (80:13:0.3 by volume), and identified with unlabeled standards in separate lanes. Lipid classes and standard bands were visualized with 6-p-toluidine-2-naphthalene-sulfonic acid (Acros, Fairlawn, NJ) under ultraviolet light. Bands were individually scraped and 200 μl toluene was added with a known amount of di-17:0-PC for quantification prior to methylation. Fatty acid methyl esters were formed by heating the phospholipid scrapes and a portion of the diet total lipid extract in 1% H2SO4 in methanol at 70°C for 3 hours [29]. The methyl esters were separated on a 30 m × 0.25 mm i.d. capillary column (SP-2330, Supelco; Bellefonte, PA), using gas chromatography with a flame ionization detector (Model 6890N, Agilent Technologies; Palo Alto, CA, USA). Runs were initiated at 80°C, with a temperature gradient to 160°C (10°C/min) and 230°C (3°C/min) in 31 min, and held at 230°C for 10 min. Peaks were identified by retention times of fatty acid methyl ester standards (Nu-Chek-Prep, Elysian, MN). Fatty acid concentrations (nmol/g brain or nmol/ml plasma) were calculated by proportional comparison of gas chromatography peak areas to that of the 17:0 internal standard.

Data and statistics

Data are presented as means ± SD, n = 6 samples per group. One-way ANOVA with Dunnett's post hoc test, comparing 24 and 12 month means to 4 month means was completed using SAS 9.0 (Cary, NC). Statistical significance was taken as p ≤ 0.05.

Competing interests

The author(s) declare that they have no competing interests.

Authors' contributions

HJL, JM and RPB carried out the analysis. HJL, RPB and SIR designed the experiment and wrote the manuscript. All authors read and approved the final manuscript.

Acknowledgments

Acknowledgements

This research was supported by the Intramural Research Program of the NIH, NIA.

Contributor Information

Ho-Joo Lee, Email: hojoolee@mail.nih.gov.

Jana Mayette, Email: jana_mayette@yahoo.com.

Stanley I Rapoport, Email: sir@helix.nih.gov.

Richard P Bazinet, Email: rbazinet@mail.nih.gov.

References

  1. Schlame M, Haldar D. Cardiolipin is synthesized on the matrix side of the inner membrane in rat liver mitochondria. J Biol Chem. 1993;268:74–79. [PubMed] [Google Scholar]
  2. Pangborn MC. The composition of cardiolipin. J Biol Chem. 1947;168:351–361. [PubMed] [Google Scholar]
  3. Rustow B, Schlame M, Rabe H, Reichmann G, Kunze D. Species pattern of phosphatidic acid, diacylglycerol, CDP-diacylglycerol and phosphatidylglycerol synthesized de novo in rat liver mitochondria. Biochim Biophys Acta. 1989;1002:261–263. doi: 10.1016/0005-2760(89)90296-8. [DOI] [PubMed] [Google Scholar]
  4. Hostetler KY, Galesloot JM, Boer P, Van Den Bosch H. Further studies on the formation of cardiolipin and phosphatidylglycerol in rat liver mitochondria. Effect of divalent cations and the fatty acid composition of CDP-diglyceride. Biochim Biophys Acta. 1975;380:382–389. doi: 10.1016/0005-2760(75)90106-x. [DOI] [PubMed] [Google Scholar]
  5. Pangborn MC. Isolation and purification of a serologically active phospholipid from beer heart. J Biol Chem. 1942;143:247–256. [Google Scholar]
  6. Schlame M, Rua D, Greenberg ML. The biosynthesis and functional role of cardiolipin. Prog Lipid Res. 2000;39:257–288. doi: 10.1016/S0163-7827(00)00005-9. [DOI] [PubMed] [Google Scholar]
  7. Hatch GM. Cell biology of cardiac mitochondrial phospholipids. Biochem Cell Biol. 2004;82:99–112. doi: 10.1139/o03-074. [DOI] [PubMed] [Google Scholar]
  8. Ioannou PV, Golding BT. Cardiolipins: their chemistry and biochemistry. Prog Lipid Res. 1979;17:279–318. doi: 10.1016/0079-6832(79)90010-7. [DOI] [PubMed] [Google Scholar]
  9. Hatch GM. Cardiolipin: biosynthesis, remodeling and trafficking in the heart and mammalian cells (Review) Int J Mol Med. 1998;1:33–41. doi: 10.3892/ijmm.1.1.33. [DOI] [PubMed] [Google Scholar]
  10. Paradies G, Ruggiero FM. Age-related changes in the activity of the pyruvate carrier and in the lipid composition in rat-heart mitochondria. Biochim Biophys Acta. 1990;1016:207–212. doi: 10.1016/0005-2728(90)90060-h. [DOI] [PubMed] [Google Scholar]
  11. Choma A, Komaniecka I. The polar lipid composition of Mesorhizobium ciceri. Biochim Biophys Acta. 2003;1631:188–196. doi: 10.1016/s1388-1981(03)00005-2. [DOI] [PubMed] [Google Scholar]
  12. Kraffe E, Soudant P, Marty Y, Kervarec N. Docosahexaenoic acid- and eicosapentaenoic acid- enriched cardiolipin in the manila clam Ruditapes philippinarum. Lipids. 2005;40:619–625. doi: 10.1007/s11745-005-1423-z. [DOI] [PubMed] [Google Scholar]
  13. Maftah A, Ratinaud MH, Dumas M, Bonte F, Meybeck A, Julien R. Human epidermal cells progressively lose their cardiolipins during ageing without change in mitochondrial transmembrane potential. Mech Ageing Dev. 1994;77:83–96. doi: 10.1016/0047-6374(94)90017-5. [DOI] [PubMed] [Google Scholar]
  14. Dyer JR, Greenwood CE. Dietary essential fatty acids change the fatty acid profile of rat neural mitochondria over time. J Nutr. 1991;121:1548–1553. doi: 10.1093/jn/121.10.1548. [DOI] [PubMed] [Google Scholar]
  15. McGee CD, Lieberman P, Greenwood CE. Dietary fatty acid composition induces comparable changes in cardiolipin fatty acid profile of heart and brain mitochondria. Lipids. 1996;31:611–616. doi: 10.1007/BF02523831. [DOI] [PubMed] [Google Scholar]
  16. Berger A, Gershwin ME, German JB. Effects of various dietary fats on cardiolipin acyl composition during ontogeny of mice. Lipids. 1992;27:605–612. doi: 10.1007/BF02536118. [DOI] [PubMed] [Google Scholar]
  17. Berger A, German JB. Phospholipid fatty acid composition of various mouse tissues after feeding alpha-linolenate (18:3n-3) or eicosatrienoate (20:3n-3) Lipids. 1990;25:473–480. doi: 10.1007/BF02538091. [DOI] [PubMed] [Google Scholar]
  18. Paradies G, Ruggiero FM, Gadaleta MN, Quagliariello E. The effect of aging and acetyl-L-carnitine on the activity of the phosphate carrier and on the phospholipid composition in rat heart mitochondria. Biochim Biophys Acta. 1992;1103:324–326. doi: 10.1016/0005-2736(92)90103-s. [DOI] [PubMed] [Google Scholar]
  19. Paradies G, Ruggiero FM, Petrosillo G, Quagliariello E. Age-dependent decrease in the cytochrome c oxidase activity and changes in phospholipids in rat-heart mitochondria. Arch Gerontol Geriatr. 1993;16:263–272. doi: 10.1016/0167-4943(93)90037-I. [DOI] [PubMed] [Google Scholar]
  20. Lewin MB, Timiras PS. Lipid changes with aging in cardiac mitochondrial membranes. Mech Ageing Dev. 1984;24:343–351. doi: 10.1016/0047-6374(84)90119-2. [DOI] [PubMed] [Google Scholar]
  21. Barcelo-Coblijn G, Collison LW, Jolly CA, Murphy EJ. Dietary alpha-linolenic acid increases brain but not heart and liver docosahexaenoic acid levels. Lipids. 2005;40 :787–789. doi: 10.1007/s11745-005-1440-y. [DOI] [PubMed] [Google Scholar]
  22. Maoz D, Lee HJ, Deutsch J, Rapoport SI, Bazinet RP. Immediate no-flow ischemia decreases rat heart nonesterified fatty acid and increases acyl-CoA species concentrations. Lipids. 2005;40:149–154. doi: 10.1007/s11745-005-1479-9. [DOI] [PubMed] [Google Scholar]
  23. Brinkmann JF, Abumrad NA, Ibrahimi A, van der Vusse GJ, Glatz JF. New insights into long-chain fatty acid uptake by heart muscle: a crucial role for fatty acid translocase/CD36. Biochem J. 2002;367:561–570. doi: 10.1042/BJ20020747. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Berger A, German JB, Gershwin ME. Implications of modifying cardiolipin acyl composition by diet. 1. Cardiolipin acyl chain is an important determinant in the binding to antiphospholipid antibodies in SLE sera. J Autoimmun. 1992;5:229–241. doi: 10.1016/0896-8411(92)90202-2. [DOI] [PubMed] [Google Scholar]
  25. Shigenaga MK, Hagen TM, Ames BN. Oxidative damage and mitochondrial decay in aging. Proc Natl Acad Sci U S A. 1994;91:10771–10778. doi: 10.1073/pnas.91.23.10771. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Reeves PG, Nielsen FH, Fahey GCJ. AIN-93 purified diets for laboratory rodents: final report of the American Institute of Nutrition ad hoc writing committee on the reformulation of the AIN-76A rodent diet. J Nutr. 1993;123:1939–1951. doi: 10.1093/jn/123.11.1939. [DOI] [PubMed] [Google Scholar]
  27. Folch J, Lees M, Sloane Stanley GH. A simple method for the isolation and purification of total lipides from animal tissues. J Biol Chem. 1957;226:497–509. [PubMed] [Google Scholar]
  28. Chang MC, Bell JM, Purdon AD, Chikhale EG, Grange E. Dynamics of docosahexaenoic acid metabolism in the central nervous system: lack of effect of chronic lithium treatment. Neurochem Res. 1999;24:399–406. doi: 10.1023/A:1020989701330. [DOI] [PubMed] [Google Scholar]
  29. Makrides M, Neumann MA, Byard RW, Simmer K, Gibson RA. Fatty acid composition of brain, retina, and erythrocytes in breast- and formula-fed infants. Am J Clin Nutr. 1994;60:189–194. doi: 10.1093/ajcn/60.2.189. [DOI] [PubMed] [Google Scholar]

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