Skip to main content
Top
Published in: Diabetologia 1/2007

01-01-2007 | Article

Increased blood–brain barrier permeability and altered tight junctions in experimental diabetes in the rat: contribution of hyperglycaemia and matrix metalloproteinases

Authors: B. T. Hawkins, T. F. Lundeen, K. M. Norwood, H. L. Brooks, R. D. Egleton

Published in: Diabetologia | Issue 1/2007

Login to get access

Abstract

Aims/hypothesis

Although diabetes mellitus is associated with peripheral microvascular complications and increased risk of neurological events, the mechanisms by which diabetes disrupts the blood–brain barrier (BBB) are not known. Matrix metalloproteinase (MMP) activity is increased in diabetic patients, is associated with degradation of tight junction proteins, and is a known mediator of BBB compromise. We hypothesise that diabetes leads to compromise of BBB tight junctions via stimulation of MMP activity.

Materials and methods

Diabetes was induced in the rat with streptozotocin. At 14 days after injection, BBB function was assessed by in situ brain perfusion. Tight junction proteins were assessed by immunoblot and immunofluorescence. Plasma MMP activity was quantified by fluorometric gelatinase assay and gel zymography.

Results

In streptozotocin-treated animals, permeability to [14C]sucrose increased concurrently with decreased production of BBB tight junction proteins occludin (also known as OCLN) and zona occludens 1 (ZO-1, also known as tight junction protein 1 or TJP1). Insulin treatment, begun on day 7, normalised blood glucose levels and attenuated BBB hyperpermeability to [14C]sucrose. Neither acute hyperglycaemia in naive animals nor acute normalisation of blood glucose in streptozotocin-treated animals altered BBB permeability to [14C]sucrose. Plasma MMP activity was increased in streptozotocin-treated animals.

Conclusions/interpretation

These data indicate that diabetes increases BBB permeability via a loss of tight junction proteins, and that increased BBB permeability in diabetes does not result from hyperglycaemia alone. Increased plasma MMP activity is implicated in degradation of BBB tight junction proteins and increased BBB permeability in diabetes. Peripheral MMP activity may present a novel target for protection of the BBB and prevention of neurological complications in diabetes.
Appendix
Available only for authorised users
Literature
1.
go back to reference Hawkins BT, Davis TP (2005) The blood–brain barrier/neurovascular unit in health and disease. Pharm Rev 57:173–185PubMedCrossRef Hawkins BT, Davis TP (2005) The blood–brain barrier/neurovascular unit in health and disease. Pharm Rev 57:173–185PubMedCrossRef
2.
go back to reference Yamagishi S, Imaizumi T (2005) Diabetic vascular complications: pathophysiology, biochemical basis and potential therapeutic strategy. Curr Pharm Des 11:2279–2299PubMedCrossRef Yamagishi S, Imaizumi T (2005) Diabetic vascular complications: pathophysiology, biochemical basis and potential therapeutic strategy. Curr Pharm Des 11:2279–2299PubMedCrossRef
3.
go back to reference Kadoglou NP, Daskalopoulou SS, Perrea D, Liapis CD (2005) Matrix metalloproteinases and diabetic vascular complications. Angiology 56:173–189PubMedCrossRef Kadoglou NP, Daskalopoulou SS, Perrea D, Liapis CD (2005) Matrix metalloproteinases and diabetic vascular complications. Angiology 56:173–189PubMedCrossRef
4.
go back to reference Ristow M (2004) Neurodegenerative disorders associated with diabetes mellitus. J Mol Med 82:510–529PubMedCrossRef Ristow M (2004) Neurodegenerative disorders associated with diabetes mellitus. J Mol Med 82:510–529PubMedCrossRef
5.
go back to reference Biessels GJ, Staekenborg S, Brunner E, Brayne C, Scheltens P (2006) Risk of dementia in diabetes mellitus: a systematic review. Lancet Neurol 5:64–74PubMedCrossRef Biessels GJ, Staekenborg S, Brunner E, Brayne C, Scheltens P (2006) Risk of dementia in diabetes mellitus: a systematic review. Lancet Neurol 5:64–74PubMedCrossRef
6.
go back to reference Starr JM, Wardlaw J, Ferguson K, MacLullich A, Deary IJ, Marshall I (2003) Increased blood–brain barrier permeability in type II diabetes demonstrated by gadolinium magnetic resonance imaging. J Neurol Neurosurg Psychiatry 74:70–76PubMedCrossRef Starr JM, Wardlaw J, Ferguson K, MacLullich A, Deary IJ, Marshall I (2003) Increased blood–brain barrier permeability in type II diabetes demonstrated by gadolinium magnetic resonance imaging. J Neurol Neurosurg Psychiatry 74:70–76PubMedCrossRef
7.
go back to reference Iwata A, Koike F, Arasaki K, Tamaki M (1999) Blood brain barrier destruction in hyperglycemic chorea in a patient with poorly controlled diabetes. J Neurol Sci 163:90–93PubMedCrossRef Iwata A, Koike F, Arasaki K, Tamaki M (1999) Blood brain barrier destruction in hyperglycemic chorea in a patient with poorly controlled diabetes. J Neurol Sci 163:90–93PubMedCrossRef
8.
go back to reference Hovsepyan MR, Haas MJ, Boyajyan AS et al (2004) Astrocytic and neuronal biochemical markers in the sera of subjects with diabetes mellitus. Neurosci Lett 369:224–227PubMedCrossRef Hovsepyan MR, Haas MJ, Boyajyan AS et al (2004) Astrocytic and neuronal biochemical markers in the sera of subjects with diabetes mellitus. Neurosci Lett 369:224–227PubMedCrossRef
9.
go back to reference Mooradian AD, Haas MJ, Batejko O, Hovsepyan M, Feman SS (2005) Statins ameliorate endothelial barrier permeability changes in the cerebral tissue of streptozotocin-induced diabetic rats. Diabetes 54:2977–2982PubMed Mooradian AD, Haas MJ, Batejko O, Hovsepyan M, Feman SS (2005) Statins ameliorate endothelial barrier permeability changes in the cerebral tissue of streptozotocin-induced diabetic rats. Diabetes 54:2977–2982PubMed
10.
go back to reference Dai J, Vrensen GF, Schlingemann RO (2002) Blood–brain barrier integrity is unaltered in human brain cortex with diabetes mellitus. Brain Res 954:311–316PubMedCrossRef Dai J, Vrensen GF, Schlingemann RO (2002) Blood–brain barrier integrity is unaltered in human brain cortex with diabetes mellitus. Brain Res 954:311–316PubMedCrossRef
11.
go back to reference Rechthand E, Smith QR, Latker CH, Rapoport SI (1987) Altered blood–nerve barrier permeability to small molecules in experimental diabetes mellitus. J Neuropathol Exp Neurol 46:302–314PubMed Rechthand E, Smith QR, Latker CH, Rapoport SI (1987) Altered blood–nerve barrier permeability to small molecules in experimental diabetes mellitus. J Neuropathol Exp Neurol 46:302–314PubMed
12.
go back to reference Ennis SR, Betz AL (1986) Sucrose permeability of the blood–retinal and blood–brain barriers. Effects of diabetes, hypertonicity, and iodate. Invest Ophthalmol Vis Sci 27:1095–1102PubMed Ennis SR, Betz AL (1986) Sucrose permeability of the blood–retinal and blood–brain barriers. Effects of diabetes, hypertonicity, and iodate. Invest Ophthalmol Vis Sci 27:1095–1102PubMed
13.
go back to reference Chehade JM, Haas MJ, Mooradian AD (2002) Diabetes-related changes in rat cerebral occludin and zonula occludens-1 (ZO-1) expression. Neurochem Res 27:249–252PubMedCrossRef Chehade JM, Haas MJ, Mooradian AD (2002) Diabetes-related changes in rat cerebral occludin and zonula occludens-1 (ZO-1) expression. Neurochem Res 27:249–252PubMedCrossRef
14.
go back to reference Antonetti DA, Barber AJ, Khin S, Lieth E, Tarbell JM, Gardner TW (1998) Vascular permeability in experimental diabetes is associated with reduced endothelial occludin content: vascular endothelial growth factor decreases occludin in retinal endothelial cells. Penn State Retina Research Group. Diabetes 47:1953–1959PubMed Antonetti DA, Barber AJ, Khin S, Lieth E, Tarbell JM, Gardner TW (1998) Vascular permeability in experimental diabetes is associated with reduced endothelial occludin content: vascular endothelial growth factor decreases occludin in retinal endothelial cells. Penn State Retina Research Group. Diabetes 47:1953–1959PubMed
15.
go back to reference Giebel SJ, Menicucci G, McGuire PG, Das A (2005) Matrix metalloproteinases in early diabetic retinopathy and their role in alteration of the blood–retinal barrier. Lab Invest 85:597–607PubMedCrossRef Giebel SJ, Menicucci G, McGuire PG, Das A (2005) Matrix metalloproteinases in early diabetic retinopathy and their role in alteration of the blood–retinal barrier. Lab Invest 85:597–607PubMedCrossRef
16.
go back to reference Derosa G, Avanzini MA, Geroldi D et al (2005) Matrix metalloproteinase 2 may be a marker of microangiopathy in children and adolescents with type 1 diabetes mellitus. Diabetes Res Clin Pract 70:119–125PubMedCrossRef Derosa G, Avanzini MA, Geroldi D et al (2005) Matrix metalloproteinase 2 may be a marker of microangiopathy in children and adolescents with type 1 diabetes mellitus. Diabetes Res Clin Pract 70:119–125PubMedCrossRef
17.
go back to reference Signorelli SS, Malaponte G, Libra M et al (2005) Plasma levels and zymographic activities of matrix metalloproteinases 2 and 9 in type II diabetics with peripheral arterial disease. Vasc Med 10:1–6PubMedCrossRef Signorelli SS, Malaponte G, Libra M et al (2005) Plasma levels and zymographic activities of matrix metalloproteinases 2 and 9 in type II diabetics with peripheral arterial disease. Vasc Med 10:1–6PubMedCrossRef
18.
go back to reference Rosenberg GA, Estrada EY, Dencoff JE (1998) Matrix metalloproteinases and TIMPs are associated with blood–brain barrier opening after reperfusion in rat brain. Stroke 29:2189–2195PubMed Rosenberg GA, Estrada EY, Dencoff JE (1998) Matrix metalloproteinases and TIMPs are associated with blood–brain barrier opening after reperfusion in rat brain. Stroke 29:2189–2195PubMed
19.
go back to reference Mun-Bryce S, Rosenberg GA (1998) Gelatinase B modulates selective opening of the blood–brain barrier during inflammation. Am J Physiol 274:R1203–R1211PubMed Mun-Bryce S, Rosenberg GA (1998) Gelatinase B modulates selective opening of the blood–brain barrier during inflammation. Am J Physiol 274:R1203–R1211PubMed
20.
go back to reference Wachtel M, Frei K, Ehler E, Fontana A, Winterhalter K, Gloor SM (1999) Occludin proteolysis and increased permeability in endothelial cells through tyrosine phosphatase inhibition. J Cell Sci 112( Pt 23):4347–4356PubMed Wachtel M, Frei K, Ehler E, Fontana A, Winterhalter K, Gloor SM (1999) Occludin proteolysis and increased permeability in endothelial cells through tyrosine phosphatase inhibition. J Cell Sci 112( Pt 23):4347–4356PubMed
21.
go back to reference Williams SA, Abbruscato TJ, Hruby VJ, Davis TP (1996) Passage of a delta-opioid receptor selective enkephalin, [d-penicillamine2,5] enkephalin, across the blood–brain and the blood–cerebrospinal fluid barriers. J Neurochem 66:1289–1299PubMedCrossRef Williams SA, Abbruscato TJ, Hruby VJ, Davis TP (1996) Passage of a delta-opioid receptor selective enkephalin, [d-penicillamine2,5] enkephalin, across the blood–brain and the blood–cerebrospinal fluid barriers. J Neurochem 66:1289–1299PubMedCrossRef
22.
go back to reference Hawkins BT, Abbruscato TJ, Egleton RD et al (2004) Nicotine increases in vivo blood–brain barrier permeability and alters cerebral microvascular tight junction protein distribution. Brain Res 1027:48–58PubMedCrossRef Hawkins BT, Abbruscato TJ, Egleton RD et al (2004) Nicotine increases in vivo blood–brain barrier permeability and alters cerebral microvascular tight junction protein distribution. Brain Res 1027:48–58PubMedCrossRef
23.
go back to reference Rozen S, Skaletsky H (2000) Primer3 on the WWW for general users and for biologist programmers. Methods Mol Biol 132:365–386PubMed Rozen S, Skaletsky H (2000) Primer3 on the WWW for general users and for biologist programmers. Methods Mol Biol 132:365–386PubMed
24.
go back to reference McReynolds MR, Taylor-Garcia KM, Greer KA, Hoying JB, Brooks HL (2005) Renal medullary gene expression in aquaporin-1 null mice. Am J Physiol Renal Physiol 288:F315–F321PubMedCrossRef McReynolds MR, Taylor-Garcia KM, Greer KA, Hoying JB, Brooks HL (2005) Renal medullary gene expression in aquaporin-1 null mice. Am J Physiol Renal Physiol 288:F315–F321PubMedCrossRef
25.
go back to reference Paxinos G, Watson C (1998) The rat brain in stereotaxic coordinates. Academic, New York Paxinos G, Watson C (1998) The rat brain in stereotaxic coordinates. Academic, New York
26.
go back to reference Willis CL, Leach L, Clarke GJ, Nolan CC, Ray DE (2004) Reversible disruption of tight junction complexes in the rat blood–brain barrier, following transitory focal astrocyte loss. Glia 48:1–13PubMedCrossRef Willis CL, Leach L, Clarke GJ, Nolan CC, Ray DE (2004) Reversible disruption of tight junction complexes in the rat blood–brain barrier, following transitory focal astrocyte loss. Glia 48:1–13PubMedCrossRef
27.
go back to reference Asahi M, Asahi K, Jung JC, del Zoppo GJ, Fini ME, Lo EH (2000) Role for matrix metalloproteinase 9 after focal cerebral ischemia: effects of gene knockout and enzyme inhibition with BB-94. J Cereb Blood Flow Metab 20:1681–1689PubMedCrossRef Asahi M, Asahi K, Jung JC, del Zoppo GJ, Fini ME, Lo EH (2000) Role for matrix metalloproteinase 9 after focal cerebral ischemia: effects of gene knockout and enzyme inhibition with BB-94. J Cereb Blood Flow Metab 20:1681–1689PubMedCrossRef
28.
go back to reference Hawkins BT, Egleton RD, Davis TP (2005) Modulation of cerebral microvascular permeability by endothelial nicotinic acetylcholine receptors. Am J Physiol, Heart Circ Physiol 289:H212–H219CrossRef Hawkins BT, Egleton RD, Davis TP (2005) Modulation of cerebral microvascular permeability by endothelial nicotinic acetylcholine receptors. Am J Physiol, Heart Circ Physiol 289:H212–H219CrossRef
29.
go back to reference Wang FQ, So J, Reierstad S, Fishman DA (2005) Matrilysin (MMP-7) promotes invasion of ovarian cancer cells by activation of progelatinase. Int J Cancer 114:19–31PubMedCrossRef Wang FQ, So J, Reierstad S, Fishman DA (2005) Matrilysin (MMP-7) promotes invasion of ovarian cancer cells by activation of progelatinase. Int J Cancer 114:19–31PubMedCrossRef
30.
go back to reference Like AA, Rossini AA (1976) Streptozotocin-induced pancreatic insulitis: new model of diabetes mellitus. Science 193:415–417PubMedCrossRef Like AA, Rossini AA (1976) Streptozotocin-induced pancreatic insulitis: new model of diabetes mellitus. Science 193:415–417PubMedCrossRef
31.
go back to reference Rakieten N, Rakieten ML, Nadkarni MR (1963) Studies on the diabetogenic action of streptozotocin (NSC-37917). Cancer Chemother Rep 29:91–98 Rakieten N, Rakieten ML, Nadkarni MR (1963) Studies on the diabetogenic action of streptozotocin (NSC-37917). Cancer Chemother Rep 29:91–98
33.
go back to reference Haffner SM, Stern MP, Hazuda HP, Mitchell BD, Patterson JK (1990) Cardiovascular risk factors in confirmed prediabetic individuals. Does the clock for coronary heart disease start ticking before the onset of clinical diabetes? JAMA 263:2893–2898PubMedCrossRef Haffner SM, Stern MP, Hazuda HP, Mitchell BD, Patterson JK (1990) Cardiovascular risk factors in confirmed prediabetic individuals. Does the clock for coronary heart disease start ticking before the onset of clinical diabetes? JAMA 263:2893–2898PubMedCrossRef
34.
35.
go back to reference Preston JE, al-Sarraf H, Segal MB (1995) Permeability of the developing blood–brain barrier to 14C-mannitol using the rat in situ brain perfusion technique. Brain Res Dev Brain Res 87:69–76PubMedCrossRef Preston JE, al-Sarraf H, Segal MB (1995) Permeability of the developing blood–brain barrier to 14C-mannitol using the rat in situ brain perfusion technique. Brain Res Dev Brain Res 87:69–76PubMedCrossRef
36.
go back to reference Witt KA, Mark KS, Hom S, Davis TP (2003) Effects of hypoxia-reoxygenation on rat blood–brain barrier permeability and tight junctional protein expression. Am J Physiol, Heart Circ Physiol 285:H2820–H2831 Witt KA, Mark KS, Hom S, Davis TP (2003) Effects of hypoxia-reoxygenation on rat blood–brain barrier permeability and tight junctional protein expression. Am J Physiol, Heart Circ Physiol 285:H2820–H2831
37.
go back to reference Maepea O, Karlsson C, Alm A (1984) Blood–ocular and blood–brain barrier function in streptozocin-induced diabetes in rats. Arch Ophthalmol 102:1366–1369PubMed Maepea O, Karlsson C, Alm A (1984) Blood–ocular and blood–brain barrier function in streptozocin-induced diabetes in rats. Arch Ophthalmol 102:1366–1369PubMed
38.
go back to reference Lorenzi M, Healy DP, Hawkins R, Printz JM, Printz MP (1986) Studies on the permeability of the blood–brain barrier in experimental diabetes. Diabetologia 29:58–62PubMedCrossRef Lorenzi M, Healy DP, Hawkins R, Printz JM, Printz MP (1986) Studies on the permeability of the blood–brain barrier in experimental diabetes. Diabetologia 29:58–62PubMedCrossRef
39.
go back to reference Hawkins BT, Fleegal MA, McCaffery G, Egleton RD (2006) Contributions of hyperglycaemia and gelatinase activity to increased blood–brain barrier permeability in experimental diabetes. Society for Neuroscience, Annual Meeting (Abstract) Hawkins BT, Fleegal MA, McCaffery G, Egleton RD (2006) Contributions of hyperglycaemia and gelatinase activity to increased blood–brain barrier permeability in experimental diabetes. Society for Neuroscience, Annual Meeting (Abstract)
40.
go back to reference Bazzoni G, Dejana E (2004) Endothelial cell-to-cell junctions: molecular organization and role in vascular homeostasis. Physiol Rev 84:869–901PubMedCrossRef Bazzoni G, Dejana E (2004) Endothelial cell-to-cell junctions: molecular organization and role in vascular homeostasis. Physiol Rev 84:869–901PubMedCrossRef
41.
go back to reference Penes MC, Li X, Nagy JI (2005) Expression of zonula occludens-1 (ZO-1) and the transcription factor ZO-1-associated nucleic acid-binding protein (ZONAB)-MsY3 in glial cells and colocalization at oligodendrocyte and astrocyte gap junctions in mouse brain. Eur J Neurosci 22:404–418PubMedCrossRef Penes MC, Li X, Nagy JI (2005) Expression of zonula occludens-1 (ZO-1) and the transcription factor ZO-1-associated nucleic acid-binding protein (ZONAB)-MsY3 in glial cells and colocalization at oligodendrocyte and astrocyte gap junctions in mouse brain. Eur J Neurosci 22:404–418PubMedCrossRef
42.
go back to reference Harkness KA, Adamson P, Sussman JD, Davies-Jones GA, Greenwood J, Woodroofe MN (2000) Dexamethasone regulation of matrix metalloproteinase expression in CNS vascular endothelium. Brain 123:698–709PubMedCrossRef Harkness KA, Adamson P, Sussman JD, Davies-Jones GA, Greenwood J, Woodroofe MN (2000) Dexamethasone regulation of matrix metalloproteinase expression in CNS vascular endothelium. Brain 123:698–709PubMedCrossRef
43.
go back to reference Jacqueminet S, Ben Abdesselam O, Chapman MJ et al (2006) Elevated circulating levels of matrix metalloproteinase-9 in type 1 diabetic patients with and without retinopathy. Clin Chim Acta 367:103–107PubMedCrossRef Jacqueminet S, Ben Abdesselam O, Chapman MJ et al (2006) Elevated circulating levels of matrix metalloproteinase-9 in type 1 diabetic patients with and without retinopathy. Clin Chim Acta 367:103–107PubMedCrossRef
44.
go back to reference Nguyen JH, Yamamoto S, Steers J et al (2005) Matrix metalloproteinase-9 contributes to brain extravasation and edema in fulminant hepatic failure mice. J Hepatol 44:1105–1114PubMedCrossRef Nguyen JH, Yamamoto S, Steers J et al (2005) Matrix metalloproteinase-9 contributes to brain extravasation and edema in fulminant hepatic failure mice. J Hepatol 44:1105–1114PubMedCrossRef
45.
go back to reference Nakaya R, Uzui H, Shimizu H et al (2005) Pravastatin suppresses the increase in matrix metalloproteinase-2 levels after acute myocardial infarction. Int J Cardiol 105:67–73PubMedCrossRef Nakaya R, Uzui H, Shimizu H et al (2005) Pravastatin suppresses the increase in matrix metalloproteinase-2 levels after acute myocardial infarction. Int J Cardiol 105:67–73PubMedCrossRef
46.
go back to reference Nomura S, Yoshimura K, Akiyama N et al (2005) HMG-CoA reductase inhibitors reduce matrix metalloproteinase-9 activity in human varicose veins. Eur Surg Res 37:370–378PubMedCrossRef Nomura S, Yoshimura K, Akiyama N et al (2005) HMG-CoA reductase inhibitors reduce matrix metalloproteinase-9 activity in human varicose veins. Eur Surg Res 37:370–378PubMedCrossRef
47.
go back to reference Couture R, Harrisson M, Vianna RM, Cloutier F (2001) Kinin receptors in pain and inflammation. Eur J Pharmacol 429:161–176PubMedCrossRef Couture R, Harrisson M, Vianna RM, Cloutier F (2001) Kinin receptors in pain and inflammation. Eur J Pharmacol 429:161–176PubMedCrossRef
48.
go back to reference Huber JD, Hau VS, Borg L, Campos CR, Egleton RD, Davis TP (2002) Blood–brain barrier tight junctions are altered during a 72-h exposure to lambda-carrageenan-induced inflammatory pain. Am J Physiol, Heart Circ Physiol 283:H1531–H1537 Huber JD, Hau VS, Borg L, Campos CR, Egleton RD, Davis TP (2002) Blood–brain barrier tight junctions are altered during a 72-h exposure to lambda-carrageenan-induced inflammatory pain. Am J Physiol, Heart Circ Physiol 283:H1531–H1537
49.
go back to reference Banks WA, Jaspan JB, Kastin AJ (1997) Effect of diabetes mellitus on the permeability of the blood–brain barrier to insulin. Peptides 18:1577–1584PubMedCrossRef Banks WA, Jaspan JB, Kastin AJ (1997) Effect of diabetes mellitus on the permeability of the blood–brain barrier to insulin. Peptides 18:1577–1584PubMedCrossRef
50.
go back to reference Mooradian AD (1987) Blood–brain barrier choline transport is reduced in diabetic rats. Diabetes 36:1094–1097PubMed Mooradian AD (1987) Blood–brain barrier choline transport is reduced in diabetic rats. Diabetes 36:1094–1097PubMed
Metadata
Title
Increased blood–brain barrier permeability and altered tight junctions in experimental diabetes in the rat: contribution of hyperglycaemia and matrix metalloproteinases
Authors
B. T. Hawkins
T. F. Lundeen
K. M. Norwood
H. L. Brooks
R. D. Egleton
Publication date
01-01-2007
Publisher
Springer-Verlag
Published in
Diabetologia / Issue 1/2007
Print ISSN: 0012-186X
Electronic ISSN: 1432-0428
DOI
https://doi.org/10.1007/s00125-006-0485-z

Other articles of this Issue 1/2007

Diabetologia 1/2007 Go to the issue