- Open Access
Chronic oral administration of minocycline to sheep with ovine CLN6 neuronal ceroid lipofuscinosis maintains pharmacological concentrations in the brain but does not suppress neuroinflammation or disease progression
Journal of Neuroinflammation volume 10, Article number: 900 (2013)
The neuronal ceroid lipofuscinoses (NCLs; or Batten disease) are fatal inherited human neurodegenerative diseases affecting an estimated 1:12,500 live births worldwide. They are caused by mutations in at least 11 different genes. Currently, there are no effective treatments. Progress into understanding pathogenesis and possible therapies depends on studying animal models. The most studied animals are the CLN6 South Hampshire sheep, in which the course of neuropathology closely follows that in affected children. Neurodegeneration, a hallmark of the disease, has been linked to neuroinflammation and is consequent to it. Activation of astrocytes and microglia begins prenatally, starting from specific foci associated with the later development of progressive cortical atrophy and the development of clinical symptoms, including the occipital cortex and blindness. Both neurodegeneration and neuroinflammation generalize and become more severe with increasing age and increasing clinical severity. The purpose of this study was to determine if chronic administration of an anti-inflammatory drug, minocycline, from an early age would halt or reverse the development of disease.
Minocycline, a tetracycline family antibiotic with activity against neuroinflammation, was tested by chronic oral administration of 25 mg minocycline/kg/day to presymptomatic lambs affected with CLN6 NCL at 3 months of age to 14 months of age, when clinical symptoms are obvious, to determine if this would suppress neuroinflammation or disease progression.
Minocycline was absorbed without significant rumen biotransformation to maintain pharmacological concentrations of 1 μM in plasma and 400 nM in cerebrospinal fluid, but these did not result in inhibition of microglial activation or astrocytosis and did not change the neuronal loss or clinical course of the disease.
Oral administration is an effective route for drug delivery to the central nervous system in large animals, and model studies in these animals should precede highly speculative procedures in humans. Minocycline does not inhibit a critical step in the neuroinflammatory cascade in this form of Batten disease. Identification of the critical steps in the neuroinflammatory cascade in neurodegenerative diseases, and targeting of specific drugs to them, will greatly increase the likelihood of success.
The neuronal ceroid lipofuscinoses (NCLs; or Batten disease) are a group of fatal inherited human neurodegenerative diseases affecting about 1:12,500 live births worldwide . NCLs are caused by over 360 mutations in at least 8 different genes responsible for childhood forms  and another 3 recently suggested to be associated with adult forms [3–5] (see http://www.ucl.ac.uk/ncl/). Affected children become blind, subject to fits and seizures and bed-ridden, and they die prematurely. Currently, there are no effective treatments for any form of the disease. Various naturally occurring or engineered animal models of the human diseases exist, the most studied large animal model being the well-characterized CLN6 South Hampshire sheep model . As in most forms of NCL, subunit c of mitochondrial ATP synthase accumulates in lysosome-derived organelles in most cells, but the biochemical mechanism of this storage is unknown [7–10].
The strength of this model is that the disease progression and course of neuropathology in affected lambs is similar to that in affected children. Affected lambs are apparently normal at birth but become blind from 10 to 14 months of age and decline until mature disease when aged about 2 years. Neurodegeneration, a hallmark of the disease, has been linked to neuroinflammation and is consequent to it. Activation of astrocytes and microglia precedes the loss of cortical neurons and progressive cortical atrophy, starting from particular neocortical foci and becoming widespread in more advanced disease [11, 12]. This results in the collapse of layers, particularly layers II to IV. Glial activation is observed perinatally in affected sheep, with reactive perivascular astrocytes being observable in the first trimester, reactive astrocytes observable in the gray matter in the third trimester and activated microglia become apparent shortly after birth . Brain atrophy is not apparent until 4 to 6 months after birth, and clinical symptoms do not develop until some months later, suggesting a potential window for anti-inflammatory therapy after birth and before neurodegeneration sets in.
Chronic inflammation is thought to be detrimental to neurons [14–16], and neuroinflammation has also been indicated as a contributing factor to various other neurodegenerative conditions , including multiple sclerosis, Alzheimer disease , Parkinson disease , HIV-associated dementia, scrapie, trauma and ischemia. A possible therapeutic option is treatment with minocycline, a second-generation antibiotic belonging to the tetracycline family, which also has anti-inflammatory activity, including activity against neuroinflammation [20, 21], and targets microglia .
Minocycline is easily absorbed when administered orally and crosses the blood–brain barrier readily. Treatment trials in both animal models and human patients have been carried out for a number of neurodegenerative diseases, including multiple sclerosis, spinal cord injury, amyotrophic lateral sclerosis, Huntington disease, Parkinson disease and Alzheimer disease, with encouraging results in a number of cases. For example, recent rodent model trials have indicated efficacy against hypoxic-ischemic brain injury , blast-induced traumatic brain injury , Alzheimer disease-like amyloid pathology  and Huntington disease-like symptoms . However, results from rodent model studies have not been very good indicators of human studies, indicating that larger animal models would be preferred, and there have also been some concerns about chronic treatment in some cases [20, 21]. Given the interaction of glial activation and neurodegeneration in the NCLs outlined above, minocycline is an obvious therapeutic candidate to be explored for treatment of the NCLs. The sheep affected by CLN6 provide a good model for this investigation, but as they are ruminants with a very active microbial rumen flora, two additional factors need to be considered, namely, the effect of the antibacterial activity on rumen function and possible rumen biotransformation of minocycline that might affect the penetration of the drug into the sheep plasma and cerebrospinal fluid (CSF).
The aims of this investigation were to determine conditions that allowed chronic administration of minocycline to a ruminant, find out if pharmacologically effective plasma and CSF concentrations of minocycline could be obtained and ascertain whether these would affect glial inflammation and the course of neurodegeneration in CLN6 Batten disease.
Materials and methods
South Hampshire heterozygous carrier ewes were mated to homozygous affected rams and lambs genotyped as carrier or affected using the disease-associated A/G polymorphism . All animals used were healthy and apparently clinically normal at the commencement of the trials. They were housed indoors in individual pens and fed a balanced commercial pelleted ration (800 g/day) and lucerne chaff (400 g/day). Age-matched heterozygous sheep were used as controls. All procedures were approved by the Lincoln University Animal Ethics Committee in compliance with the New Zealand Animal Welfare Act (1999) and in accordance with US National Institutes of Health guidelines.
Minocycline administration and animal monitoring
Minocycline hydrochloride (100 to 150 g; Archimica S.r.L., Origgio, Italy) was dissolved in 100 ml of dimethyl sulfoxide, then diluted in 30% animal feed grade molasses to 200 mg/ml. Aliquots were stored at −20°C. This solution was sprayed onto daily rations to deliver the required dose.
In the therapy trial, three 3-month-old affected rams began receiving minocycline in molasses at 2 mg/kg/day and two controls received molasses only. The minocycline dosage was increased stepwise to 25 mg/kg/day over 6 weeks, which was maintained for a further 5 months, then lowered to 16 mg/kg/day for a further 4 months, after which the animals were killed.
Animals were weighed weekly during their growth phase and then at 2- to 3-week intervals, and minocycline dosages adjusted accordingly. Every 6 to 8 weeks, sheep were anesthetized with intravenously administered 1:1 ketamine:diazepam (ketamine, Phoenix Ketamine, Auckland, NZ; and diazepam, Pamlin, Parnell Laboratories, East Tamaki, NZ) before taking cerebrospinal fluid (CSF) samples from the cisterna magnum, jugular blood samples and computed tomography (CT) scans for brain volume determinations. After 3 months of drug administration, possible liver damage was assessed from the serum activities of γ-glutamyltransferase and glutamate dehydrogenase, determined by Gribbles Veterinary Pathology, Auckland, NZ.
Minocycline high-performance liquid chromatography
Minocycline extracted from plasma and CSF was analyzed by high-performance liquid chromatography (HPLC) . Aliquots (500 μl) of plasma, CSF and standards (0.08 to 10.12 μM minocycline in plasma or CSF) were diluted with 750 μl of sodium phosphate sulfite buffer (2.4 M disodium hydrogen phosphate, 4.0 M sodium sulfite, pH 6.5) and thoroughly mixed with 4 ml of ethyl acetate. After centrifugation to separate the phases, the aqueous phase was frozen and the organic phase was poured off into 50 μl of 0.2% ascorbic acid and 0.1% cysteine in methanol. Samples were dried at 39°C under nitrogen, and the residue was dissolved in 250 μl of running buffer, an 85:12:3 mixture of a solution of 0.1 M potassium nitrite, 0.05 M citric acid and 0.033 M sodium citrate:dimethylformamide:ethyl acetate. After centrifugation, 10,000 rpm, 2 min, 50-μl aliquots were injected onto a Brava BDS C8 column W 100 (4.6 mm × 3 μm; Grace Davison Discovery Sciences, Deerfield, IL, USA) in an Agilent HPLC fitted with a diode display array detector (Agilent 1100 Series; Agilent Technologies, Walbronn, Germany) and eluted with running buffer at 0.5 ml/min. Minocycline, retention time 8.2 to 8.4 min, was detected at 350 nm (Figure 1). The mean ± SD extraction efficiency for minocycline was 64.2 ± 4.5%. All elution peaks with a retention time of 6 min or more were scanned from 250 to 450 nm, and the spectra were compared to plasma and CSF standards to detect any minocycline metabolites.
Clinical assessment of vision
Vision was scored weekly by awareness of hand movement on a scale of apparent normal awareness = 15, subnormal awareness = 10, marginal awareness = 5 and no awareness = 0.
Assessment of brain atrophy
CT scans were performed under anesthesia in a GE ProSpeed CT Scanner (GE Healthcare, Hyogo, Japan). Coronal slices 1 mm thick were scanned at 5-mm intervals, 120 kV, 160 mA, 2 s, and brain volumes were determined by using the Cavalieri method from the areas of each slice. Volumes from the experimental animals, determined every 6 to 8 weeks, were compared with those of a cohort of normal, unaffected sheep.
Assessment of brain pathology
Brains were perfusion fixed in 10% formalin immediately post-mortem, divided down the midline, equilibrated in cryoprotectant solution (10% ethylene glycol and 30% sucrose in saline) at 4°C and stored frozen. Serial sagittal sections 50 μm thick were cut on a sliding freezing microtome (Microm GmbH, Walldorf, Germany) and stored individually at –20°C in 100 μl of cryoprotectant in 96-well plates as described previously [12, 13]. Nissl staining and immunostaining were done on floating sections. Microglia and astrocytes were detected using biotinylated α-D-galactose-specific isolectin I-B4 from Griffonia simplicifolia (GSB4; Vector Laboratories, Peterborough, UK) and anti-glial fibrillary acidic protein (anti-GFAP; Dako, Carpinteria, CA, USA), respectively, and diluted in 0.2% Triton X-100 in phosphate-buffered saline (PBST) containing 1% normal goat serum. Biotinylated anti-rabbit secondary antibody (Sigma-Aldrich, St Louis, MO, USA) was diluted 1:1,000 in the same buffer. Sections were washed three times with PBST solution containing 1% normal goat serum for 3 h, and antibody and lectin binding were detected using horseradish peroxidase (ExtrAvidin; Sigma-Aldrich) and diaminobenzidine tetrahydrochloride in 0.1 M acetate buffer at pH 6.0.
Layer thickness measurements on the brain sections were determined using SPOT software (SPOT Imaging Solutions, Sterling Heights, MI, USA). All analyses and images were of the visual cortex and occipital lobe, the regions first and most affected by neurodegeneration . Measurements were made from the pial surface of the cortex to the layer V–VI boundary since sheep layer VI is difficult to define in affected brains and measurements from layers I to V cover the entire gray matter apart from this difficult-to-see layer. The distances from layers II to V were also measured since layer I is the least affected by neurodegeneration  so comparisons of layers II to V offer the most sensitive measure of any protective effect of minocycline on neuronal layers.
GSB4 and GFAP immunoreactivities in the cortical region encompassing neuronal layers II to V in sections of the visual cortex of affected treated and untreated animals were captured for image analysis by using a Nikon Digital Sight DSFi1 camera attached to a Nikon Eclipse 50i microscope (Nikon Instruments, Tokyo, Japan). Data were analyzed after threshold analysis using NIS-Elements Advanced Research version 3.0 software (Nikon Instruments). Three different fields per section per animal were analyzed (pixel classifier), and the results are expressed as percentage per unit area.
An effective dosing regimen was developed that gave the rumen flora time to adjust to the antibiotic activity of minocycline and resulted in pharmacologically sensible plasma and CSF concentrations of untransformed minocycline. This regimen involved increasing dietary minocycline from an initial dose of only 2 mg/kg/day. A higher initial dosing of 4 mg/kg/day caused a sharp drop in feed intake and was halted. For the therapy trial, three 3.4-month-old affected ram lambs accustomed to molasses began receiving minocycline at 2 mg/kg/day. The dosage was then increased stepwise to 25 mg minocycline/kg/day at 4.5 months of age, which was maintained for 5 months and then lowered to 16 mg/kg/day for a further 5 months, at the end of which time the brains were perfusion-fixed for sectioning and microscopy.
This treatment did not affect liver function, with the serum activities of the liver enzymes γ-glutamyltransferase and glutamate dehydrogenase of both the treated and control affected sheep being within the normal ranges for healthy sheep after 3 months of chronic treatment. Drug treatment did not alter feed consumption, and the increase in body weight of the treated animals of 1.7 kg/mo was not significantly different from 2.1 kg/mo for untreated animals.
Easily measurable plasma and CSF concentrations of the drug resulted, with the 8.2- to 8.3-minute retention time HPLC elution peak being separated from other absorbing components. It had the 250- to 450-nm absorption spectrum of minocycline and was identical in both plasma and CSF samples from the experimental sheep and plasma and CSF spiked with unmodified minocycline (Figure 1), indicating that pharmacologic amounts of the untransformed drug passed through the rumen, were absorbed into serum and were partitioned into the CSF. Rises in plasma and CSF concentrations of minocycline lagged behind the dosing program, and plateau concentrations were not reached until week 25 of treatment while the dose was 25 mg/kg/day. The highest concentrations detected, 2,563 nM and 700 nM, respectively, dropped subsequent to the daily dietary dose being lowered from 25 to 16 mg/kg/day. Mean ± SEM minocycline concentrations over the entire treatment period were 1,000 ± 223 nM in plasma and 390 ± 61 nM in CSF.
CSF concentrations of minocycline were always lower than those of matching plasma samples, suggesting that the minocycline entered the brain via the plasma and left via the CSF, but the relationship between them was not linear and a logarithmic function best fitted the data (Figure 2). The CSF-to-plasma concentration ratio was high, up to 0.78, at low plasma concentrations (less than 500 nM) and low, 0.2 to 0.3, at plasma concentrations greater than 1,500 nM. Minocycline distribution was widespread throughout the animals, with the bones, particularly the skull and ribs, being noticeably yellow post-mortem.
Clinical and pathological effects
Year-long treatment at these pharmacologically relevant concentrations of minocycline in plasma and CSF had no observable effect on the development of symptoms or pathology in the affected sheep. Treatment did not alter the development of blindness. Both the treated and untreated affected sheep scored maximum points for visual awareness up to the age of 9 months, then visual awareness declined to zero in both groups by 15 months of age. The rate of gross brain atrophy was not altered by minocycline treatment either. Brain volumes of both the treated and untreated affected sheep, determined by regular CT scanning, were almost static. At the beginning of the experiments, the brain volume for the treated group was 90.7 ± 6 ml (mean ± SD) compared with 88.5 ± 3 ml for the untreated animals, and these volumes remained virtually unchanged, being 89.6 ± 2 ml and 88.6 ± 2 ml respectively after 15 months. These data are in contrast to the increase in normal sheep brain volumes, from 90 ml to 104 ml, over the same age span.
Neurodegeneration was also assessed by measurements on Nissl-stained sections of the thickness from the pia and the neuron-rich boundary of layers I and II to the easily identifiable boundary between layer V pyramidal neurons and layer VI multiform neurons. These distances were chosen because the layer V–VI is easy to locate, whereas the bottom of layer VI is difficult to identify. Because layer I is the least affected , a second measurement, of layers II to V, was also made. These distances were similar in both treated and untreated affected animals and were about 20% less than in normal control brains (Table 1).
There was also no indication that the chronic minocycline treatment reduced neuroinflammation. Numerous activated amoeboid single microglial cells or clusters of microglia were densely concentrated in bands incorporating cortical layers II and III and layers V and VI of both treated and untreated affected brains (Figure 3). Similar neurodegeneration was also indicated by the similar widths of the GBS4 immunopositive band of cells in the cortex (Table 1). Normal control brains contained no GSB4-reactive microglia. GFAP-positive activated astrocytes bearing thickened and intensely immunostained processes were distributed fairly evenly across the six cortical layers in both the treated and untreated affected brains, but not in unaffected control brains. Quantitative threshold analyses of GSB4 and GFAP confirmed that the treatment had no effect on microglial activation or astrocytosis. Immunoreactivities in the cortical region encompassing neuronal layers II to V in the visual cortex of minocycline-treated and untreated affected animals (± SD, n = 3) were 38.0 ± 8.7% and 36.6 ± 6.9%, respectively, for GSB4, and 67.9 ± 12.7% and 63.7 ± 5.4%, respectively, for GFAP.
Sheep became readily accustomed to chronic incremental oral administration of minocycline without any indication of intolerance or ill effects, and, once established, oral administration was simpler and caused fewer concerns than either intraperitoneal or intravenous injection . Any disturbance to the rumen flora, possibly caused by the antibiotic activity of this drug, was transient, and accustomed sheep ate readily and grew at the same rate as controls. The HPLC elution profile and ultraviolet-visible spectra of peaks (Figure 1) gave no indication of minocycline metabolites in either the CSF or sera, including no evidence of the most likely ones, 9-hydroxyminocycline and N-demethylated minocycline . Furthermore, sufficient amounts of the drug were circulating to establish concentrations of about 380 nM and 1 μM in the CSF and serum, respectively, a ratio seen in other species [30, 31]. On the basis of the brain-to-unbound plasma minocycline ratios of 2.6 to 2.8 reported previously [32, 33], the brain concentrations of minocycline in treated sheep were likely to be about 670 nM for the year-long treatment.
Prolonged treatment at this dose did not change the course of the disease, however, despite beginning at an early preclinical age before neurodegeneration had begun. Glial activation commences in utero and continues into adulthood in these sheep , but loss of cortical neurons does not commence until a little later, at about 5 months of age. The experiments were designed to take advantage of this possible window of opportunity in which suppression of microglial activation might slow or halt the onset of the neurodegeneration and associated disease processes. Treatment started after the animals were weaned at about 3 months of age, but all markers of progress of the disease were unchanged by it. The loss of visual awareness was similar in the treated and affected control animals, as was brain atrophy, with treated and untreated animals losing about 0.4 ml of brain volume per month compared to a gain of 1 ml per month in normal animals. Minocycline did not influence progressive microglial activation or progressive cortical gray matter loss either (Table 1 and Figure 3). This is unlikely to be due to a lack of penetration of minocycline into the brain. It was evident from the yellowing of the bones that the drug was widely distributed in the sheep, and, judging from in vitro studies, concentrations of 60 μM to 200 nM should be sufficient [33–35]; thus the CSF concentrations of 380 nM achieved in the current study were expected to be sufficient.
It may be that chronic neuroinflammation does not respond to minocycline inhibition. Normally, reactive gliosis in response to an insult is acute and associated with a cascade of proinflammatory cytokines. Microglia numbers increase and then return to pre-insult numbers [36, 37]. A number of studies have shown that induced pro-inflammatory cytokines IL-lα and TNF-α [38–41] decline with minocycline treatment in these situations, but the timing of treatment relative to the initial brain insult may be important. In most instances described, minocycline treatment was commenced prior to experimental insults, [22, 38–40, 42–44]. Neuroinflammation commences in the second half of gestational life in these sheep ; thus, although minocycline treatment began relatively early at weaning, it may have been too late to be effective.
Neuroinflammation in the CLN6 affected sheep is widespread and sustained, and there are mixed reports of anti-inflammatory drugs being effective in these situations [18, 45, 46], suggesting that the chronic inflammatory process is difficult to subdue or that drugs targeted to the critical steps are required. For instance, high-dose intraperitoneal administration of minocycline resulted in an 80% to 90% decline of pro-inflammatory cytokines after a Staphylococcus aureus insult, but no reduction of microglial activation .
These data highlight the complexity of the neuroinflammatory cascade and of targeting suppression of it. Apart from the observation of microglial activation and astrocytosis, little is known of the inflammatory pathway in Batten disease, and it is unclear what triggers neuroinflammation in these sheep. It is unlikely that dead and dying neurons are the trigger, as neuronal loss only starts at 5 months of age , some 6 months after the first observation of activated cortical glia , and the abnormal accumulation of storage bodies containing subunit c is also unlikely to be the trigger. These accumulate ubiquitously throughout the brain, whereas the neuroinflammation is highly regional. Some areas of the brain, such as the hypothalamus, have extensive storage body accumulation but exhibit no neuroinflammation, even at advanced disease stages . It is also now clear from work in other animal models of different forms of Batten disease that neuron loss is invariably preceded by localized glial activation , also noted in two canine NCL models  and a mouse model of neuronopathic Gaucher disease . By extension, it is unlikely that minocycline treatment alone will be effective for the treatment of these other forms of Batten disease.
It is clear from the above discussion that more needs to be known of the mechanism of the glial activation in the NCLs and which particular parts of the inflammation pathways are critically involved. Studies are underway to address this by determining the regional distribution and activities of cytokines and other inflammation-linked processes in the brains of affected sheep over time. Greater knowledge of the mechanism of action of anti-inflammatory agents would also enhance targeting of therapies by indicating which drugs might be effective. Presently, it is not clear where minocycline acts. A number of studies in mice have shown that induced proinflammatory cytokines such as TNF-α decline with minocycline treatment [38, 41], perhaps by inhibition of the p38 mitogen-activated protein kinase (p38 MAPK) pathway. Among other possibilities suggested for minocycline action are down-regulation of major histocompatibility complex II expression through interferon regulatory factor 1 (IRF-1) and protein kinase C α/βII (PKCα/βII) inhibition , inhibition of secretory phospholipase A2 indicated by structural studies , neuroprotection by direct scavenging of peroxynitrite  and reduction of several other inflammatory factors .
This study has established that oral administration is an effective route for drug delivery to the CNS in ruminants as well as the utility of large animal model studies, which should precede highly speculative procedures in already compromised humans. A case in point is the recent abandonment of minocycline treatment of human Huntington’s disease that had been encouraged by positive results of murine studies . However, this does not preclude a role for anti-inflammatory neuroprotection in the treatment of the NCLs with correctly targeted drugs alone or in combination with other treatments, such as gene therapy. More precise knowledge of the critical steps in the neuroinflammatory cascade and targeting of specific drugs to inhibit them will greatly increase the likelihood of success.
α-D-galactose-specific isolectin I-B4 from Griffonia simplicifolia
Glial fibrillary acidic protein
High-performance liquid chromatography
- p38 MAPK:
p38 mitogen-activated protein kinase
Tumor necrosis factor α.
Rider JA, Rider DL: Batten disease: past, present, and future. Am J Med Genet 1988, Suppl 5:21–26.
Kousi M, Lehesjoki AE, Mole SE: Update of the mutation spectrum and clinical correlations of over 360 mutations in eight genes that underlie the neuronal ceroid lipofuscinoses. Hum Mutat 2012, 33:42–63.
Bras J, Verloes A, Schneider SA, Mole SE, Guerreiro RJ: Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosis. Hum Mol Genet 2012, 21:2646–2650.
Nosková L, Stránecký V, Hartmannová H, Přistoupilová A, Barešová V, Ivánek R, Hůlková H, Jahnová H, van der Zee J, Staropoli JF, Sims KB, Tyynelä J, Van Broeckhoven C, Nijssen PC, Mole SE, Elleder M, Kmoch S: Mutations in DNAJC5 , encoding cysteine-string protein alpha, cause autosomal-dominant adult-onset neuronal ceroid lipofuscinosis. Am J Hum Genet 2011, 89:241–252.
Smith KR, Dah HHM, Canafoglia L, Andermann E, Damiano J, Morbin M, Bruni AC, Giaccone G, Cossette P, Saftig P, Grötzinger J, Schwake M, Andermann F, Staropoli JF, Sims KB, Mole SE, Franceschetti S, Alexander NA, Cooper JD, Chapman HA, Carpenter S, Berkovic SF, Bahlo M: Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis. Hum Mol Genet 2013, 22:1417–1423.
Tammen I, Houweling PJ, Frugier T, Mitchell NL, Kay GW, Cavanagh JAL, Cook RW, Raadsma HW, Palmer DN: A missense mutation (c.184C > T) in ovine CLN6 causes neuronal ceroid lipofuscinosis in Merino sheep whereas affected South Hampshire sheep have reduced levels of CLN6 mRNA. Biochim Biophys Acta 2006, 1762:898–905.
Palmer DN, Martinus RD, Cooper SM, Midwinter GG, Reid JC, Jolly RD: Ovine ceroid-lipofuscinosis. The major lipopigment protein and the lipid-binding subunit of mitochondrial ATP synthase have the same NH 2 -terminal sequence. J Biol Chem 1989, 264:5736–5740.
Palmer DN, Fearnley IM, Walker JE, Hall NA, Lake BD, Wolfe LS, Haltia M, Martinus RD, Jolly RD: Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease). Am J Med Genet 1992, 42:561–567.
Chen R, Fearnley IM, Palmer DN, Walker JE: Lysine 43 is trimethylated in subunit c from bovine mitochondrial ATP synthase and in storage bodies associated with Batten disease. J Biol Chem 2004, 279:21883–21887.
Palmer DN, Tammen I, Drögemüller C, Johnson GS, Katz ML, Lingaas F: Large animal models. In The neuronal ceroid lipofuscinoses (Batten disease). 2nd edition. Edited by: Mole SE, Williams RE, Goebel HH. New York: Oxford University Press; 2011:284–320.
Oswald MJ, Palmer DN, Kay GW, Barwell KJ, Cooper JD: Location and connectivity determine GABAergic interneuron survival in the brains of South Hampshire sheep with CLN6 neuronal ceroid lipofuscinosis. Neurobiol Dis 2008, 32:50–65.
Oswald MJ, Palmer DN, Kay GW, Shemilt SJA, Rezaie P, Cooper JD: Glial activation spreads from specific cerebral foci and precedes neurodegeneration in presymptomatic ovine neuronal ceroid lipofuscinosis (CLN6). Neurobiol Dis 2005, 20:49–63.
Kay GW, Palmer DN, Rezaie P, Cooper JD: Activation of non-neuronal cells within the prenatal developing brain of sheep with neuronal ceroid lipofuscinosis. Brain Pathol 2006, 16:110–116.
Raivich G, Bohatschek M, Kloss CUA, Werner A, Jones LL, Kreutzberg GW: Neuroglial activation repertoire in the injured brain: graded response, molecular mechanisms and cues to physiological function. Brain Res Rev 1999, 30:77–105.
Stoll G, Jander S: The role of microglia and macrophages in the pathophysiology of the CNS. Prog Neurobiol 1999, 58:233–247.
Streit WJ, Mrak RE, Griffin WST: Microglia and neuroinflammation: a pathological perspective. J Neuroinflammation 2004, 1:14.
Neumann H: Control of glial immune function by neurons. Glia 2001, 36:191–199.
Eikelenboom P, Veerhuis R, Scheper W, Rozemuller AJM, van Gool WA, Hoozemans JJM: The significance of neuroinflammation in understanding Alzheimer’s disease. J Neural Transm 2006, 113:1685–1695.
Kim YS, Joh TH: Microglia, major player in the brain inflammation: their roles in the pathogenesis of Parkinson’s disease. Exp Mol Med 2006, 38:333–347.
Blum D, Chtarto A, Tenenbaum L, Brotchi J, Levivier M: Clinical potential of minocycline for neurodegenerative disorders. Neurobiol Dis 2004, 17:359–366.
Kim HS, Suh YH: Minocycline and neurodegenerative diseases. Behav Brain Res 2009, 196:168–179.
Yrjänheikki J, Keinänen R, Pellikka M, Hökfelt T, Koistinaho J: Tetracyclines inhibit microglial activation and are neuroprotective in global brain ischemia. Proc Natl Acad Sci (USA) 1998, 95:15769–15774.
Reinebrant HE, Wixey JA, Buller KM: Disruption of raphé serotonergic neural projections to the cortex: a potential pathway contributing to remote loss of brainstem neurons following neonatal hypoxic-ischemic brain injury. Eur J Neurosci 2012, 36:3483–3491.
Kovesdi E, Kamnaksh A, Wingo D, Ahmed F, Grunberg NE, Long JB, Kasper CE, Agoston DV: Acute minocycline treatment mitigates the symptoms of mild blast-induced traumatic brain injury. Front Neurol 2012, 3:111.
Ferretti MT, Allard S, Partridge V, Ducatenzeiler A, Cuello AC: Minocycline corrects early, pre-plaque neuroinflammation and inhibits BACE-1 in a transgenic model of Alzheimer’s disease-like amyloid pathology. J Neuroinflammation 2012, 9:62.
Kalonia H, Mishra J, Kumar A: Targeting neuro-inflammatory cytokines and oxidative stress by minocycline attenuates quinolinic-acid-induced Huntington’s disease-like symptoms in rats. Neurotox Res 2012, 22:310–320.
Pijpers A, Schoevers EJ, Haagsma N, Verheijden JH: Plasma levels of oxytetracycline, doxycycline, and minocycline in pigs after oral administration in feed. J Anim Sci 1991, 69:4512–4522.
Fagan SC, Edwards DJ, Borlongan CV, Xu L, Arora A, Feuerstein G, Hess DC: Optimal delivery of minocycline to the brain: implication for human studies of acute neuroprotection. Expt Neurol 2004, 186:248–251.
Böcker RH, Peter R, Machbert G, Bauer W: Identification and determination of the two principal metabolites of minocycline in humans. J Chromatogr 1991, 568:363–374.
Agwuh KN, MacGowan A: Pharmacokinetics and pharmacodynamics of the tetracyclines including glycylcyclines. J Antimicrob Chemother 2006, 58:256–265.
Barza M, Brown RB, Shanks C, Gamble C, Weinstein L: Relation between lipophilicity and pharmacological behaviour of minocycline, doxycycline, tetracycline, and oxytetracycline in dogs. Antimicrob Agents Chemother 1975, 8:713–720.
Aronson AL: Pharmacotherapeutics of the newer tetracyclines. J Am Vet Med Assoc 1980, 176:1061–1068.
Kremlev SG, Roberts RL, Palmer C: Differential expression of cytokines and chemokine receptors during microglial activation and inhibition. J Neuroimmunol 2004, 149:1–9.
Tikka TM, Koistinaho JE: Minocycline provides neuroprotection against N -methyl-D-aspartate neurotoxicity by inhibiting microglia. J Immunol 2001, 166:7527–7533.
Wang AL, Yu ACH, Lau LT, Lee C, Wu LM, Zhu XA, Tso MOM: Minocycline inhibits LPS-induced retinal microglia activation. Neurochem Internat 2005, 47:152–158.
Graeber MB, Streit WJ: Microglia: biology and pathology. Acta Neuropathol 2010, 119:89–105.
Streit WJ, Xue QS: Life and death of microglia. J Neuroimmune Pharmacol 2009, 4:371–379.
Sriram K, Miller DB, O’Callaghan JP: Minocycline attenuates microglial activation but fails to mitigate striatal dopaminergic neurotoxicity: role of tumor necrosis factor-α. J Neurochem 2006, 96:706–718.
Tomás-Camardiel M, Rite I, Herrera AJ, de Pablos RM, Cano J, Machado A, Venero JL: Minocycline reduces the lipopolysaccharide-induced inflammatory reaction, peroxynitrite-mediated nitration of proteins, disruption of the blood–brain barrier, and damage in the nigral dopaminergic system. Neurobiol Dis 2004, 16:190–201.
Yrjänheikki J, Tikka T, Keinänen R, Goldsteins G, Chan PH, Koistinaho J: A tetracycline derivative, minocycline, reduces inflammation and protects against focal cerebral ischemia with a wide therapeutic window. Proc Natl Acad Sci (USA) 1999, 96:13496–13500.
Zhao C, Ling Z, Newman MB, Bhatia A, Carvey PM: TNF-α knockout and minocycline treatment attenuates blood–brain barrier leakage in MPTP-treated mice. Neurobiol Dis 2007, 26:36–46.
Henry CJ, Huang Y, Wynne A, Hanke M, Himler J, Bailey MT, Sheridan JF, Godbout JP: Minocycline attenuates lipopolysaccharide (LPS)-induced neuroinflammation, sickness behaviour and anhedonia. J Neuroinflammation 2008, 5:15.
Wu DC, Jackson-Lewis V, Vila M, Tieu K, Teismann P, Vadseth C, Choi DK, Ischiropoulos H, Przedborski S: Blockade of microglial activation is neuroprotective in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine mouse model of Parkinson disease. J Neurosci 2002, 22:1763–1771.
Boger HA, Middaugh LD, Granholm AC, McGinty JF: Minocycline restores striatal tyrosine hydroxylase in GDNF heterozygous mice but not in methamphetamine-treated mice. Neurobiol Dis 2009, 33:459–466.
McGeer PL, McGeer EG: NSAIDs and Alzheimer disease: epidemiological, animal model and clinical studies. Neurobiol Aging 2006, 28:639–647.
Tuppo EE, Arias HR: The role of inflammation in Alzheimer’s disease. Internat J Biochem Cell Biol 2005, 37:289–305.
Kielian T, Esen N, Lui S, Phulwani NK, Syed MM, Phillips N, Nishina K, Cheung AL, Schwartzman JD, Ruhe JJ: Minocycline modulates neuroinflammation independently of its antimicrobial activity in Staphylococcus aureus -induced brain abscess. Am J Pathol 2007, 171:1199–1214.
Kay GW, Jay NP, Palmer DN: The specific loss of GnRH-positive neurons from the hypothalamus of sheep with CLN6 neuronal ceroid lipofuscinosis occurs without glial activation and has only minor effects on reproduction. Neurobiol Dis 2011, 41:614–623.
Cooper JD: The neuronal ceroid lipofuscinoses: the same, but different? Biochem Soc Trans 2010, 38:1448–1452.
Nibe K, Nakayama H, Uchida K: Comparative study of cerebellar degeneration in canine neuroaxonal dystrophy, cerebellar cortical abiotrophy, and neuronal ceroid-lipofuscinosis. J Vet Med Sci 2010, 72:1495–1499.
Farfel-Becker T, Vitner EB, Pressey SNR, Eilam R, Cooper JD, Futerman AH: Spatial and temporal correlation between neuron loss and neuroinflammation in a mouse model of neuronopathic Gaucher disease. Hum Mol Genet 2011, 20:1375–1386.
Nikodemova M, Watters JJ, Jackson SJ, Yang SK, Duncan ID: Minocycline down-regulates MHC II expression in microglia and macrophages through inhibition of IRF-1 and protein kinase C (PKC) α/βII . J Biol Chem 2007, 282:15208–15216.
Dalm D, Palm GJ, Aleksandrov A, Simonson T, Hinrichs W: Nonantibiotic properties of tetracyclines: structural basis for inhibition of secretory phopholipase A 2 . J Mol Biol 2010, 398:83–96.
Schildknecht S, Pape R, Müller N, Robotta M, Marquardt A, Bürkle A, Drescher M, Leist M: Neuroprotection by minocycline caused by direct and specific scavenging of peroxynitrite. J Biol Chem 2011, 286:4991–5002.
Garwood CJ, Cooper JD, Hanger DP, Noble W: Anti-inflammatory impact of minocycline in a mouse model of tauopathy. Front Psychiatry 2010,1(136):1–8.
Schwarz H, Hickey C, Zimmerman C, Mazzoni P, Moskowitz C, Rosas D, McCall M, Sanchez-Ramos J, Perlmutter J, Wernle A, Higgins D, Nickerson C, Evans S, Kumar R, Miracle D, Dure L, Pendley D, Anderson K, Cines M, Ashizawa T, Stanton P, Fernandez H, Suelter M, Leavitt B, Decolongon J, Cudkowicz M, McDermott MP, Kieburtz K, Marshall F, Cha JH, Huntington Study Group DOMINO Investigators, et al.: A futility study of minocycline in Huntington’s disease. Mov Disord 2010, 25:2219–2224.
This work was supported by US National Institutes of Health grant NS053559 as well as grants from the Batten Disease Support and Research Association and the Neurological Foundation of New Zealand. We thank Nigel Jay, Nadia Mitchell, Rosie Tung and Jenny Zhao for their technical assistance and Abheek Chakraborty for preliminary minocycline HPLC analyses.
The authors declare that they have no competing interests.
GWK carried out or supervised the experimental work and provided draft material for the MS. DNP organized the funding and resources, managed the project, and wrote and produced the MS. Both authors read and approved the final manuscript.
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Kay, G.W., Palmer, D.N. Chronic oral administration of minocycline to sheep with ovine CLN6 neuronal ceroid lipofuscinosis maintains pharmacological concentrations in the brain but does not suppress neuroinflammation or disease progression. J Neuroinflammation 10, 900 (2013). https://doi.org/10.1186/1742-2094-10-97
- Anti-inflammatory drugs
- Batten disease
- Cerebrospinal fluid
- Cortical atrophy
- Ovine model