Biology:Superoxide dismutase mimetics

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Short description: Synthetic compounds

Superoxide dismutase (SOD) mimetics are synthetic compounds that mimic the native superoxide dismutase enzyme.[1] SOD mimetics effectively convert the superoxide anion (O−2), a reactive oxygen species, into hydrogen peroxide, which is further converted into water by catalase.[2] Reactive oxygen species are natural byproducts of cellular respiration and cause oxidative stress and cell damage, which has been linked to causing cancers, neurodegeneration, age-related declines in health, and inflammatory diseases.[3][4] SOD mimetics are a prime interest in therapeutic treatment of oxidative stress because of their smaller size, longer half-life, and similarity in function to the native enzyme.[3][5][6]

The chemical structure of SOD mimetics generally consists of manganese, iron, or copper (and zinc) coordination complexes.[1][3][7] Salen-manganese(III) complexes contain aromatic ring structures that increase the lipid solubility and cell permeability of the entire complex.[2] Manganese (II) and iron (III) complexes are commonly used due to their high kinetic and thermodynamic stability, increasing the half-life of the mimetic.[1] However, manganese-based SOD mimetics are found to be more therapeutically effective than their counterparts due to their low toxicity, higher catalytic activity, and increased stability in vivo.[1][3][7]

Dismutation of superoxide anions with a metal-based catalyzer (denoted by M) in a redox cycle. The Mn and Mn-1 show the oxidized and reduced forms of the metallic center, respectively. The metallic center is able to convert a superoxide anion to oxygen in the first half reaction by accepting an electron. In the second half reaction, the reduced metal atom donates the electron to another superoxide anion in order to form hydrogen peroxide, regenerating the metal ion in its original oxidation state.

Mechanism of action

Similar to the native enzyme’s mechanism,[8] the manganese complexes undergo a reversible oxidation/reduction cycle.[2] In the first half reaction manganese covalently coordinates to the superoxide anion on its oxygen binding site,[2] through inner-sphere electron transfer.[3] (Mn) is reduced by superoxide, yielding molecular oxygen and a reduced form of manganese (Mn-1). The metal (Mn-1) is then regenerated to its former oxidation state (Mn) by reducing a second superoxide molecule to hydrogen peroxide.[9]

1. Mn + O−2 → Mn-1 + O2
2. Mn-1 + O−2 + 2H+ → Mn + H2O2
Net: Mn + 2O−2 + 2H+ → Mn + O2 + H2O2

The metal complex must be electron deficient in nature, allowing it to accept electrons from the superoxide.[10] This is accomplished by coordinating electron-withdrawing ligands around the metal center.[10] Since the mechanism of SOD mimetics involves a redox cycle, the catalytic activity of the SOD mimetic is partially dependent on the reduction potential of the metal center.[9] Coordinated ligands of SOD mimetics fine-tune the chemical properties of the complex[3] and are designed to match the 300mV reduction potential of the native enzyme.[11]

Manganese-based SODs

The most prominent SOD mimetics are: manganese porphyrin complexes, manganese (II) penta-azamacrocyclic complexes, and manganese (III) salen complexes.[4]

Manganese porphyrin

Rotating model of MnTBAP (Mn(III)tetrakis (4-benzoic acid) porphyrin), a manganese-porphyrin compound with proposed superoxide dismutase activity. Grey, blue, red, purple, and white balls represent carbon, nitrogen, oxygen, manganese, and hydrogen atoms, respectively. The counter ion has been omitted from the structure.

Porphyrin SOD mimetics consist of manganese (III) centers coordinated by a single porphyrin ring.[10] Although both complexes are effective porphyrin-based superoxide dismutases, MnTBAP [Mn(III)tetrakis (4-benzoic acid) porphyrin] was shown to better protect the cells from oxidative damages compared to ZnTBAP ((Zinc (III) tetrakis (4-benzoic acid)porphyrin chloride)) in vivo.[7] Researchers found MnTBAP reversed obesity[12] and induced faster wound healing in diabetic mice.[13] MnTBAP has the ability to prevent formation of cytotoxic peroxynitrite,[14] a hazardous byproduct of superoxide reacting with nitric oxide, and induces healing process of wounds.[13] MnTMPyP [manganese (III) tetrakis (1-methyl-4-pyridyl) porphyrin], another porphyrin molecule, was also found effective in relieving oxidative stress caused by peroxynitrite in intracellular and extracellular conditions.[15] Manganese-porphyrin complexes reduced the damaging effects of radiation treatment in mice.[4]

Manganese (II) penta-azamacrocyclic: M40401/3

Rotating model of M40401, a manganese-containing superoxide dismutase mimic. Grey, blue, purple, and white balls represent carbon, nitrogen, manganese, and hydrogen atoms, respectively. The counter ion has been omitted from the structure.

M40403 and M40401 are Manganese (II) Penta-Azamacrocyclic complexes with SOD mimetic properties.[16] Mn (II) complexes are found to be more stable in vivo and have high specificity for the superoxide anion, preventing unwanted interactions with biologically important molecules.[1] They are characterized as having a small size, high stability, and higher catalytic efficiency than superoxide dismutase, especially in more acidic environments.[1][16] M40403 was found effective in reducing oxidative tissue damage induced by total body irradiation.[16] M40401 is similar in structure to M40403, but it has two additional methyl groups, causing a one hundredfold increase in catalytic activity in treatment of ischemia-reperfusion injuries.[17] M40401 was also found to protect against hypoxic-ischemic brain injury.[6]

Manganese (III) salen

Mn (III) Salen complexes are found to be more stable than other iron or manganese mimics of superoxide dismutase.[2] In certain synthesized forms, aromatic rings are coordinated with the manganese center, increasing the lipid solubility of the entire complex, allowing it to pass the cellular membrane.[2]

Life-span extension

Treatment of the nematode Caenorhabditis elegans with superoxide dismutase/catalase (SOD/catalase) mimetics has been reported to extend life-span.[18][19] Mice with deficient SOD2 die prematurely, exhibiting severe metabolic and mitochondrial defects. Treatment of such mice with SOD/catalase mimetics extended their life-span by as much as three-fold.[20] Treatment of wild-type mice with a carboxyfullerene SOD mimetic not only reduced age-associated oxidative stress and mitochondrial radical production, but significantly extended life-span.[5] This treatment also rescued age-related cognitive impairment. These findings suggest that oxidative stress is an important determinant of life-span.

References

  1. ↑ 1.0 1.1 1.2 1.3 1.4 1.5 "Superoxide Dismutase Mimetics". Pulmonary Pharmacology & Therapeutics 15 (5): 439–447. 2002. doi:10.1006/pupt.2002.0374. PMID 12406666. 
  2. ↑ 2.0 2.1 2.2 2.3 2.4 2.5 Baudry, M; Etienne, S; Bruce, A; Palucki, M; Jacobsen, E; Malfroy, B (30 April 1993). "Salen-Manganese Complexes Are Superoxide Dismutase-Mimics". Biochemical and Biophysical Research Communications 192 (2): 964–68. Retrieved 10 January 2015.
  3. ↑ 3.0 3.1 3.2 3.3 3.4 3.5 "Comparative studies on manganese-based SOD mimetics, including the phosphate effect, by using global spectral analysis". Journal of Inorganic Biochemistry 109: 26–32. 2012. doi:10.1016/j.jinorgbio.2011.12.008. PMID 22366231. 
  4. ↑ 4.0 4.1 4.2 Vujaskovic, Zeljko; Batinic-Haberle, Ines; Rabbani, Zahid N; Feng, Qin-fu; Kang, Song K; Spasojevic, Ivan; Samulski, Thaddeus V; Fridovich, Irwin et al. (2002). "A small molecular weight catalytic metalloporphyrin antioxidant with superoxide dismutase (SOD) mimetic properties protects lungs from radiation-induced injury". Free Radical Biology and Medicine (Elsevier BV) 33 (6): 857–863. doi:10.1016/s0891-5849(02)00980-2. ISSN 0891-5849. PMID 12208373. 
  5. ↑ 5.0 5.1 "A carboxyfullerene SOD mimetic improves cognition and extends the lifespan of mice". Neurobiol. Aging 29 (1): 117–28. January 2008. doi:10.1016/j.neurobiolaging.2006.09.014. PMID 17079053. 
  6. ↑ 6.0 6.1 "Neuroprotection against hypoxia-ischemia in neonatal rat brain by novel superoxide dismutase mimetics". Neuroscience Letters 346 (1–2): 41–4. 2003. doi:10.1016/S0304-3940(03)00558-5. PMID 12850543. 
  7. ↑ 7.0 7.1 7.2 "A metalloporphyrin superoxide dismutase mimetic protects against paraquat-induced endothelial cell injury, in vitro.". J Pharmacol Exp Ther 275 (3): 1227–32. 1995. PMID 8531085. 
  8. ↑ "Superoxide dismutases: active sites that save, but a protein that kills". Current Opinion in Chemical Biology 8 (2): 162–68. 2004. doi:10.1016/j.cbpa.2004.02.011. PMID 15062777. 
  9. ↑ 9.0 9.1 "Impact of electrostatics in redox modulation of oxidative stress by Mn porphyrins: Protection of SOD-deficient Escherichia coli via alternative mechanism where Mn porphyrin acts as a Mn carrier". Free Radical Biology and Medicine 45 (2): 201–10. 2008. doi:10.1016/j.freeradbiomed.2008.04.009. PMID 18457677. 
  10. ↑ 10.0 10.1 10.2 "Diverse functions of cationic Mn(III) N-substituted pyridylporphyrins, recognized as SOD mimics". Free Radical Biology and Medicine 51 (5): 1035–53. 2011. doi:10.1016/j.freeradbiomed.2011.04.046. PMID 21616142. 
  11. ↑ Crapo, James; Day, Brian; Fridovich, Irwin. "Development of Manganic Porphyrin Mimetics of Superoxide Dismutase Activity". Madame Curie Bioscience Database [Internet]. Landes Bioscience. Retrieved 31 January 2015.
  12. ↑ "A new class of anti-obesity compounds with potential anti-diabetic properties". 17 April 2012. https://www.kurzweilai.net/a-new-class-of-anti-obesity-compounds-with-potential-anti-diabetic-properties. 
  13. ↑ 13.0 13.1 "Therapeutic administration of superoxide dismutase (SOD) mimetics normalizes wound healing in diabetic mice". Journal of the American College of Surgeons 201 (3): S57. 2005. doi:10.1016/j.jamcollsurg.2005.06.124. 
  14. ↑ "Beneficial effects of Mn(III)tetrakis (4-benzoic acid) porphyrin (MnTBAP), a superoxide dismutase mimetic, in carrageenan-induced pleurisy". Free Radical Biology and Medicine 26 (1–2): 25–33. 1999. doi:10.1016/s0891-5849(98)00142-7. PMID 9890637. 
  15. ↑ "Loss of endothelium-derived nitric oxide in rabbit aorta by oxidant stress: restoration by superoxide dismutase mimetics". British Journal of Pharmacology 124 (4): 719–28. 1998. doi:10.1038/sj.bjp.0701899. PMID 9690864. 
  16. ↑ 16.0 16.1 16.2 "The manganese superoxide dismutase mimetic, M40403, protects adult mice from lethal total body irradiation". Free Radical Research 44 (5): 529–40. 2010. doi:10.3109/10715761003649578. PMID 20298121. 
  17. ↑ "Protective effects of a new stable, highly active SOD mimetic, M40401in splanchnic artery occlusion and reperfusion". British Journal of Pharmacology 132 (1): 19–29. 2001. doi:10.1038/sj.bjp.0703775. PMID 11156557. 
  18. ↑ "Extension of life-span with superoxide dismutase/catalase mimetics". Science 289 (5484): 1567–9. September 2000. doi:10.1126/science.289.5484.1567. PMID 10968795. Bibcode: 2000Sci...289.1567M. 
  19. ↑ "Effects of a potent antioxidant, platinum nanoparticle, on the lifespan of Caenorhabditis elegans". Mech. Ageing Dev. 129 (6): 322–31. June 2008. doi:10.1016/j.mad.2008.02.011. PMID 18400258. 
  20. ↑ "Lifespan extension and rescue of spongiform encephalopathy in superoxide dismutase 2 nullizygous mice treated with superoxide dismutase-catalase mimetics". J. Neurosci. 21 (21): 8348–53. November 2001. doi:10.1523/jneurosci.21-21-08348.2001. PMID 11606622. 



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