Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...
Reexamination Certificate
1998-03-25
2001-10-23
Raymond, Richard L. (Department: 1624)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Having -c-, wherein x is chalcogen, bonded directly to...
C548S421000
Reexamination Certificate
active
06306889
ABSTRACT:
BACKGROUND OF THE INVENTION
1. Field of the Invention
The invention relates to the prevention and treatment of neural or cardiovascular tissue damage resulting from ischemia and reperfusion injury. More particularly, the invention concerns the prevention or treatment of vascular stroke by administering inhibitors of the nucleic enzyme poly(ADP-ribose) polymerase or “PARP”, which is also sometimes called “PARS” for poly(ADP-ribose) synthetase.
2. Description of the Prior Art
Poly(ADP-ribose) polymerase (“PARP”) is an enzyme located in the nuclei of cells of various organs, including muscle, heart and brain cells. PARP plays a physiological role in the repair of strand breaks in DNA. Once activated by damaged DNA fragments, PARP catalyzes the attachment of up to 100 ADP-ribose units to a variety of nuclear proteins, including histones and PARP itself. While the exact range of functions of PARP has not been established, this enzyme is thought to play a role in enhancing DNA repair.
During major cellular stresses, however, the extensive activation of PARP can rapidly lead to cell death through depletion of energy stores. Four molecules of ATP are consumed for every molecule of NAD (the source of ADP-ribose) regenerated. Thus, NAD, the substrate of PARP, is depleted by massive PARP activation and, in the efforts to re-synthesize NAD, ATP may also be depleted.
PARP activation plays a key role in both NMDA- and NO-induced neurotoxicity, as shown by the use of PARP inhibitors to prevent such toxicity in cortical cultures in proportion to their potencies as inhibitors of this enzyme (Zhang et al., “Nitric Oxide Activation of Poly(ADP-Ribose) Synthetase in Neurotoxicity”,
Science,
263:687-89 (1994)) and in hippocampal slices (Wallis et al., “Neuroprotection Against Nitric Oxide Injury with Inhibitors of ADP-Ribosylation”,
NeuroReport,
5:3, 245-48 (1993)). The potential role of PARP inhibitors in treating neurodegenerative diseases has thus been known.
Large numbers of known PARP inhibitors have been described in Banasik et al., “Specific Inhibitors of Poly(ADP-Ribose) Synthetase and Mono(ADP-Ribosyl)transferase”,
J. of Biol. Chem.,
267:3, 1569-75 (1992), and in Banasik et al., “Inhibitors and Activators of ADP-Ribosylation Reactions”,
Molec. and Cell. Biochem.
138:185-97 (1994).
It has been demonstrated that single injections of PARP inhibitors have reduced the infarct size caused by ischemia and reperfusion of the heart or skeletal muscle in rabbits. In these studies, a single injection of the PARP inhibitor, 3-aminobenzamide (10 mg/kg), either one minute before occlusion or one minute before reperfusion, caused similar reductions in infarct size in the heart (32-42%). Another PARP inhibitor, 1,5-dihydroxyisoquinoline (1 mg/kg), reduced infarct size by a comparable degree (38-48%). Thiemermann et al., “Inhibition of the Activity of Poly(ADP Ribose) Synthetase Reduces Ischemia-Reperfusion Injury in the Heart and Skeletal Muscle”,
Proc. Natl. Acad. Sci. USA,
94:679-83 (1997). This finding has suggested that PARP inhibitors might be able to salvage previously ischemic heart or skeletal muscle tissue.
PARP activation has also been shown to provide an index of damage following neurotoxic insults by glutamate (via NMDA receptor stimulation), reactive oxygen intermediates, amyloid &bgr;-protein, n-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) and its active metabolite N-methyl-4-phenylpyridine (MPP
+
), which participate in such pathological conditions as stroke, Alzheimer's disease and Parkinson's disease. Zhang et al., “Poly(ADP-Ribose) Synthetase Activation: An Early Indicator of Neurotoxic DNA Damage”,
J. of Neurochem.,
65:3, 1411-14 (1995).
Neural damage following stroke and other neurodegenerative processes is thought to result from a massive release of the excitatory neurotransmitter glutamate, which acts upon the N-methyl-D-aspartate (NMDA) receptors and other subtype receptors. Evidence includes findings in many animal species, as well as in cerebral cortical cultures treated with glutamate or NMDA, that glutamate receptor antagonists block neural damage following vascular stroke. Dawson et al., “Protection of the Brain from Ischemia”,
Cerebrovascular Disease,
319-25 (Batjer ed. 1997).
The stimulation of NMDA receptors, in turn, activates the enzyme neuronal nitric oxide synthase (nNOS), which causes the formation of nitric oxide (NO), which more directly mediates neurotoxicity. Protection against NMDA neurotoxicity has occurred following treatment with NOS inhibitors. See Dawson et al., “Nitric Oxide Mediates Glutamate Neurotoxicity in Primary Cortical Cultures”,
Proc. Natl. Acad. Sci. USA,
88:6368-71 (1991); and Dawson et al., “Mechanisms of Nitric Oxide-mediated Neurotoxicity in Primary Brain Cultures”,
J. Neurosci.,
13:6, 2651-61 (1993). Protection against NMDA neurotoxicity can also occur in cortical cultures from mice with targeted disruption of nNOS. See Dawson et al., “Resistance to Neurotoxicity in Cortical Cultures from Neuronal Nitric Oxide Synthase-Deficient Mice”,
J. Neurosci.,
16:2479-87 (1996). It is known that neural damage following vascular stroke is markedly diminished in animals treated with NOS inhibitors or in mice with nNOS gene disruption. Iaddcola, “Bright and Dark Sides of Nitric Oxide in Ischemic Brain Injury”,
Trends Neurosci.
20:3, 132-39 (1997); and Huang et al., “Effects of Cerebral Ischemia in Mice Deficient in Neuronal Nitric Oxide Synthase”,
Science,
265:1883-85 (1994). See Beckman et al., “Pathological Implications of Nitric Oxide, Superoxide and Peroxynitrite Formation”,
Biochem. Soc. Trans.,
21:330-34 (1993). Either NO or peroxynitrite can cause DNA damage, which activates PARP.
Zhang et al., U.S. Pat. No. 5,587,384 issued Dec. 24, 1996 discusses the use of certain PARP inhibitors, such as benzamide and 1,5-dihydroxyisoquinoline, to prevent NMDA-mediated neurotoxicity and, thus, treat stroke, Alzheimer's disease, Parkinson's disease and Huntington's disease. See also, Zhang et al. “Nitric Oxide Activation of Poly(ADP-Ribose) Synthetase in Neurotoxicity”,
Science,
263:687-89 (1994).
However, the approach of using these PARP inhibitors to reduce NMDA-receptor stimulation or to treat or prevent tissue damage caused by NO is limited in effect. For example, side effects have been observed with some of the best-known PARP inhibitors, as discussed in Milam et al., “Inhibitors of Poly(Adenosine Diphosphate-Ribose) Synthesis: Effect on Other Metabolic Processes”,
Science,
223:589-91 (1984). Specifically, the PARP inhibitors 3-aminobenzamide and benzamide not only inhibited the action of PARP but also were shown to affect cell viability, glucose metabolism, and DNA synthesis. Thus, it was concluded that the usefulness of these PARP inhibitors may be severely restricted by the difficulty of finding a dose small enough to inhibit the enzyme without producing additional metabolic effects.
Certain related compounds have been disclosed for medical treatments and other uses. However, these compounds are structurally distinguishable and directed to uses which emphasize their toxic characteristics. Fernandez et al., PCT publication WO 95/29895, discloses an isoquinoline derivative which is used as an anticancer agent. Desilets et al., “Design and Synthesis of Near-Infrared Absorbing Pigments”,
Can. J. Chem.
(1995), 73:3, 319-35, disclose the design and synthesis of near-infrared absorbing pigments such as aceanthrene green and derivatives. Langlois et al., “Synthesis of Quinazoline-2,4-dione and Naphthalimide Derivatives as New S-HT
3
Receptor Antagonists”,
Eur. J. Med. Chem.
(1994), 29:12, 925-940, disclose the preparation and 5-HT
3
receptor antagonist activity of certain quinazolinediones, benzisoquinolinones, and -diones. Simmonds, British Patent GB1545767 (1975) disclose benzopyranoisoquinoline derivatives useful for anti-inflammatory and central nervous system activity and also disclose a related compound useful only as an intermediate in making these distinct compounds. Kardos et al., Ger
Jackson Paul F.
Li Jia-He
Maclin Keith M.
Zhang Jie
Guilford Pharmaceuticals Inc.
Nixon & Vanderhye PC
Raymond Richard L.
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