- Open Access
Minocycline ameliorates cognitive impairment induced by whole-brain irradiation: an animal study
© Zhang et al.; licensee BioMed Central Ltd. 2014
Received: 19 September 2014
Accepted: 28 November 2014
Published: 12 December 2014
It has been long recognized that cranial irradiation used for the treatment of primary and metastatic brain tumor often causes neurological side-effects such as intellectual impairment, memory loss and dementia, especially in children patients. Our previous study has demonstrated that whole-brain irradiation (WBI) can cause cognitive decline in rats. Minocycline is an antibiotic that has shown neuroprotective properties in a variety of experimental models of neurological diseases. However, whether minocycline can ameliorate cognitive impairment induced by ionizing radiation (IR) has not been tested. Thus this study aimed to demonstrate the potential implication of minocycline in the treatment of WBI-induced cognitive deficits by using a rat model.
Sprague Dawley rats were cranial irradiated with electron beams delivered by a linear accelerator with a single dose of 20 Gy. Minocycline was administered via oral gavages directly into the stomach before and after irradiation. The open field test was used to assess the anxiety level of rats. The Morris water maze (MWM) was used to assess the spatial learning and memory of rats. The level of apoptosis in hippocampal neurons was measured using immunohistochemistry for caspase-3 and relative markers for mature neurons (NeuN) or for newborn neurons (Doublecortin (DCX)). Neurogenesis was determined by BrdU incorporation method.
Neither WBI nor minocycline affected the locomotor activity and anxiety level of rats. However, compared with the sham-irradiated controls, WBI caused a significant loss of learning and memory manifest as longer latency to reach the hidden platform in the MWM task. Minocycline intervention significantly improved the memory retention of irradiated rats. Although minocycline did not rescue neurogenesis deficit caused by WBI 2 months post-IR, it did significantly decreased WBI-induced apoptosis in the DCX positive neurons, thereby resulting in less newborn neuron depletion 12 h after irradiation.
Minocycline significantly inhibits WBI-induced neuron apoptosis, leading to less newborn neurons loss shortly after irradiation. In the long run, minocycline improves the cognitive performance of rats post WBI. The results indicate a potential clinical implication of minocycline as an effective adjunct in radiotherapy for brain tumor patients.
As an important treatment modality for primary and metastatic brain tumors, cranial irradiation often causes neurological side-effects such as intellectual impairment, memory loss and dementia, especially in children patients -. The cognitive decline has been suggested to be due to radiation-induced deficits in the hippocampal-dependent functions of learning, memory and spatial information processing -. Although the mechanisms underlying radiation-induced cognitive impairment remain to be elucidated, the studies using radiation-induced learning and memory deficit animal models have shown that the decline of hippocampal-dependent functions is generally accompanied by hippocampal apoptosis ,, decreased hippocampal proliferation ,, reduced neurogenesis ,, and marked alteration in neurogenic microenvironment ,.
In attempt to alleviate the neurotoxicity of radiotherapy for brain tumor patients and improve the quality of their life after treatment, intense effort is being made to develop the methods that can attenuate radiation-induced cognitive impairment. For example, exercise ,, transplantation of human fetal-derived neural stem cells , and some pharmacological agents such as Lithium compound ,, have been shown to improve cognitive function post irradiation.
Minocycline, a clinical available antibiotic, has been demonstrated to be neuro-protective in animal models of several acute central neural system (CNS) injuries and neurodegenerative diseases ,. In the present study, we tested whether minocycline could inhibit radiation-induced cognitive decline. We found that minocycline intervention significantly attenuated the learning and memory loss caused by whole-brain irradiation (WBI) 2 months post-irradiation. Our short-term study showed that minocycline significantly prevented hippocampal neurons, especially DCX+ neurons from WBI-induced apoptosis 6 hours post-irradiation, thus leading to less newborn neurons loss. However, minocycline had no effect on neurogenesis deficit 2 months after WBI. The results indicate a potential implication for minocycline in ameliorating radiation-induced cognitive dysfunction.
Animals and experimental groups
All animal procedures were carried out in accordance with Soochow University Medical Experimental Animal Care Guidelines based on the National Animal Ethical Policies. One-month-old male Sprague Dawley rats weighing 90-110 g (obtained from the Experimental Animal Center of Soochow University) were used as described previously . The animals were housed in cages at an ambient temperature of 22 ± 1°C with a 12-h light-dark cycle. Pelleted rat chow and tap water were available ad libitum.
Rats were randomly allocated into six groups: untreated control (CN), minocycline (CM), sham control (SCN), sham minocycline (SCM), radiation (RN) and minocycline plus radiation (RM) (n = 18/group except the SCN and SCM groups which had n = 12/group). The CN group or the CM group received only saline or minocycline, respectively; The SCN group or the SCM group were subjected to the radiation procedure with 0 Gy in addition to receiving saline or minocycline. The CN, CM, SCN and SCM groups are referred as the control groups in the text. The RN group or the RM group were subjected to WBI in addition to the treatment with either saline or minocycline.
One day before radiation, rats received either a total dose of 90 mg/kg of clinical grade minocycline (100 mg/capsule, Huishi Pharmaceutical Ltd. Co., P. R. China) dissolved in saline in 2 divided doses or the same volume of physiological saline alone (vehicle, 4.5 ml/kg) via oral gavages directly into the stomach. After irradiation, animals were administered with either saline or minocycline twice daily (45 mg/kg/d) for 2 months .
Prior to irradiation, animals were anesthetized with 3.6% chloral hydrate (360 mg/kg, i.p.). Then the WBI was performed using 4-MeV electron beams delivered by a linear accelerator (Philips SL − 18, Philips, UK) at room temperature (RT), as described previously . Briefly, a 20 × 20 cm lead shielding block with 10 holes specifically cut for WBI was used. The size of each hole was ~ 3.5 × 2.0 cm (length × width). One hole was for one rat brain. The other parts of rat’s body were shielded with the lead block. For irradiated rats, a single WBI dose of 20 Gy was given at a dose rate of 210-220 cGy/min.
General observation and body weight gain
After irradiation, rats were monitored for their motor activity, feeding and drinking behavior, as well as the side effects such as nausea, ataxia, and topical skin reaction. Their body weights were recorded biweekly. All these observations were recorded and used as parameters of general changes after treatment.
Open field test
Since the level of anxiety could affect the performance of learning and memory test, open field test was used to assess the anxiety level of all groups as described previously . Briefly, three days after 2-month minocycline intervention, open field test was performed in a silent dimly lit room. The open field used in this study, which was a square sound proof chamber (410 × 410 × 505 mm), was made of Plexiglas so that rats were visible from outside of the chamber. The floor of the chamber was divided into 25 8 × 8 cm squares, and the area that contained 9 squares in the middle was called the central region. A video camera was placed above the center of the open field. The rats were placed in the central region and allowed to move freely and to explore the environment for 10 min. The movements were recorded by computer-aided video-tracking system (Jiliang, Shanghai, China). The total distance rats traveled around the open field area and the time they spent in the central region of the open field were analyzed. After each individual test, the apparatus was cleaned with 10% ethanol thoroughly to remove any olfactory cues.
Morris water maze (MWM)
The MWM is generally used to assess the spatial learning and memory of rats . The experimental apparatus, which is a circular water tank (160 cm diameter, Jiliang, Shanghai, China) filled with opaque water (22 ± 1°C), and has a hidden submerged platform (9 cm diameter) in the center of the target quadrant , was used to assess the ability of a rat to locate the platform. The rats were placed into each of the 4 quadrants of the pool for 60 s, and were trained to locate the submerged hidden platform. They had to find the platform using only the distal spatial cues available in the testing room. When failed, the rats were gently placed on the platform for 10 s. The time rats spent on searching and mounting the platform (i.e. latency) and their swim speeds were recorded by video-tracking system (Jiliang, Shanghai, China). After 4 days of place navigation tests, a 30-s spatial probe test (the submerged platform removed) was performed on day 5. The time rats spent on crossing the target quadrant and all four quadrants were recorded for 30 s by the tracking system.
Assessment of neurogenesis by BrdU incorporation
Four weeks after sham or WBI treatment, the rats were injected intraperitoneally with a dose of BrdU (50 mg/kg, Sigma, St Louis, MO, USA) daily for 6 consecutive days. Three weeks after the last dose of BrdU, rats were sacrificed and the brain tissues were harvested and processed using the method below for analysis of neurogenesis.
Tissue preparation and immunohistochemistry
Rats were sacrificed at 3, 6 or 12 h after irradiation for apoptosis measurement or 2 months post-irradiation for neurogenesis studies. To remove the brains, anesthetized rats were transcardially perfused with PBS followed by decapitation, then the brains were placed in 10% paraformaldehyde solution for 24 h. A single 5-mm-thick section containing the hippocampus was dissected and paraffin-embedded, and the brain levels were approximately 125 ± 150 μm apart as previously described . At least ten non-overlapping coronal sections (4 μm) were cut from three different brain levels by using a RM 2135 microtome (Leica, Germany) and mounted on poly-L-lysine-coated slides.
The tissue sections were processed as previously described  and double stained with mouse monoclonal anti-NeuN (specific to human, mouse, rat and chicken NeuN, 1:100, Millipore, USA) or goat anti-DCX antibodies (specific to mouse, rat and human DCX, 1:50, Santa Cruz, USA) and rabbit polyclonal anti-active caspase-3 antibodies (specific to mouse, rat, human and quail active caspase-3, 1:15, Abcam, UK). After incubation with primary antibodies, the sections were washed and incubated sequentially with their respective secondary antibodies for 1.5 hours at RT, which are Alexa Fluor® 594 donkey anti-mouse secondary antibodies (1:100, Invitrogen, USA) for NeuN or Cy3 donkey anti-goat secondary antibodies (1:250, Beyotime, China) for DCX and Alexa Fluor® 488 donkey anti-rabbit secondary antibodies (1:150, Invitrogen, USA) for activated caspase-3. Then the sections were washed in PBS, counter stained with 4′,6′-diamidimo-2-phenylindole (DAPI, Sigma-Aldrich, USA) and sealed with nail polish. The number of NeuN/active caspase-3 double positive cells in the granule cell layer (GCL) and DCX/active caspase-3 double positive cells within the subgranular zone (SGZ) of the suprapyrimidal and infrapyrimidal blades of the dentate gyrus were scored blindly using a histomorphometric approach  under a fluorescent microscope (DM 2000, Leica, Germany).
For analysis of neurogenesis in the SGZ, the sections were dual-immunostained with NeuN and BrdU (1:120, Abcam, UK) antibodies. Then the sections were washed and sequentially incubated with the secondary antibody for NeuN and Alexa Fluor® 488 donkey anti-rat secondary antibody (1:200, Invitrogen, USA) for BrdU for 1.5 hours at RT. After washing, the sections were also stained with DAPI. Cell counts were limited to the GCL and a 50-μm border along the hilar margin that included the SGZ. And all samples were scored blindly. For each animal, five to six sections from three regions of the hippocampus were analyzed. The total number of positively labeled cells was determined by adding up the numbers of positive cells in both dentate gyri from all analyzed sections in the same rat. And all immunofluorescent images were captured using a Nikon confocal fluorescent microscope (A1, Japan).
The results were expressed as mean ± SEM. The cognitive study data were analyzed via one-way ANOVA followed by a Tukey post hoc test for multiple comparison using OriginPro Software (v8.0). And the immunohistochemical study data were analyzed using two-sample t-test. A P < 0.05 between groups was considered significantly different.
General observation and body weight gain
Minocycline ameliorated radiation-induced cognition impairment
Minocycline did not improve hippocampal neurogenesis deficit 2 months post-irradiation
Minocycline decreased radiation-induced apoptosis in neurons shortly after WBI
DCX+ neurons existed in large numbers in the SGZ, averaging 1583 ± 63 DCX+ neurons in sham-irradiated animals. Irradiation significantly reduced the number of DCX+ neurons in the SGZ by 47%, 72% and 85% for 3, 6 and 12 h post-IR, respectively (P < 0.001), and minocycline treatment caused a recovery in the number of DCX-positive cells by 28.4% (P = 0.007) at 3 h after irradiation (Figure 6B). The recovery was not observed at 6 h post-irradiation. But by 12 h after radiation, the number of DCX+ neurons in the SGZ in the RM group was 91% greater than that in the RN group (P = 0.009) (Figure 6B), suggesting that minocycline intervention could facilitate preservation of DCX+ neurons in the SGZ post-irradiation.
Cranial radiation therapy often causes neurological side-effects including cognitive impairment. Our study has demonstrated for the first time that minocycline, a clinical available antibiotic, can significantly improve the learning and memory loss in rats caused by WBI. Further studies show that minocycline intervention does not have any protective effects on neurogenesis deficit 2 months post-irradiation. However, we found that minocycline can protect the newborn and immature neurons in the dentate SGZ from radiation-induced apoptosis, thus resulting in less newborn neuron depletion shortly after WBI.
The MWM has been used to reveal a severe spatial navigation deficit in the adult rats receiving a single high dose of X-rays (8-9 Gy) shortly after birth . Using the same assay, our previous study has also showed a significant cognition decline in rats exposed to X-irradiation at one-month old . In the present study, using MWM we found that minocycline intervention significantly attenuated cognitive decline in irradiated rats (Figure 2D). Since the learning and memory performance of rats could be affected by their anxiety and motor activity, we also measured their levels of anxiety and swimming speeds, and found that both irradiation and minocycline did not affect them. Thus we could rule out the contribution of anxiety and motor activity to WBI-induced cognitive decline and the protective effect of minocycline in rats.
The mechanisms underlying the decline of cognitive function is unclear, although accumulated evidence suggests that reduced hippocampal neurogenesis adversely affects memory formation -. Consistent with previous report ,, our results demonstrated that radiation-induced learning and memory deficit was accompanied with significant decline of neurogenesis. However, no protective effects of minocycline on neurogenesis was observed in spite of its recovery effect on the learning and memory performance in irradiated rats. The effect of minocycline on neurogenesis seems somewhat controversial. The study from Kohman et al.  showed that minocycline may recover some aspects of cognitive decline associated with aging, but the effect appears to be unrelated to adult hippocampal neurogenesis. Ng et al. found that despite the attenuation of activated microglia, minocycline do not support neurogenesis in the hippocampus . However, Mattei et al. recently reported that minocycline rescues decrease in neurogenesis in an animal model of schizophrenia .
Moreover, we found that WBI-induced cognitive impairment was accompanied with severe neuron apoptosis, especially apoptosis in the newborn and immature neurons in the dentate SGZ, which agrees with the previous studies ,. Minocycline did not have strong protective effects on radiation-induced apoptosis in mature neurons in the dentate GCL (Figure 4A). In contrast, minocycline protected the newborn and immature neurons in the dentate SGZ from radiation-induced apoptosis (Figures 5A and 6A), thereby resulting in less newborn neuron depletion 12 h after radiation (Figure 6B). This is similar to the previous report that pretreatment with minocycline mitigated isoflurane-induced cognitive deficits and suppressed the isoflurane-induced caspase-3 activation and apoptosis in the hippocampus 4 h after isoflurane exposure . The neuroprotective properties of minocycline have been suggested to be due to its direct antioxidant activity, which is as good as Vitamin E . It has been shown that ionizing radiation can induce caspase-3-dependent apoptosis through generation of reactive oxygen species (ROS) in Neural stem cells . Thus an antioxidant like minocycline could inhibit caspase-3-dependent apoptosis by scavenging ROS. Although Mizumatus et al. showed that acute dose-related changes in SGZ precursor cells qualitatively correlate with later decreases in new neuron production after radiation, and suggested that precursor cell radiation response may play a contributory if not causative role in radiation-induced cognitive impairment , linking radiation-induced acute damage in hippocampus at early times to the progressive cognitive impairment at late times after radiation is still difficult. Therefore, despite our results, at this time we are unlikely to be able to draw the conclusion that the recovery effect of minocycline on the decline of cognitive function of rats 2 months post-irradiation was due to its protective effect on neurons from radiation-induced apoptosis shortly after WBI.
It was suggested that the alleviating effect of minocycline on long-term spatial memory impairment in aged mice was associated with the inhibition of astrocytic activation . In addition, minocycline was found to reduce astrocytic reactivation and neuroinflammation in the hippocampus of a vascular cognitive impairment rat model . Therefore, whether the mechanisms underlying the protective effects of minocycline on radiation-induced cognitive impairment involves inhibition of astrocytic activation and neuroinflammation needs to be elucidated in the further studies.
In summary, we have found minocycline, a clinical available antibiotic, does not affect normal growth, and significantly attenuates irradiation-induced cognitive impairment and protects newborn neurons from radiation-induced apoptosis, leading to less new neuron loss. The results indicate a potential clinical implication of minocycline as an effective adjunct in radiotherapy for brain tumor patients.
This research was supported by the National Natural Science Foundation of China grants (81172128, 81102077, 81372411, 81472804), Jiangsu Provincial Special Program of Clinical Medical Science (BL2014040), Jiangsu Province’s Key Medical Department in 2011 and A Project Funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions (PARD).
- DeAngelis LM, Delattre JY, Posner JB: Radiation-induced dementia in patients cured of brain metastases. Neurology 1989, 39: 789-796. 10.1212/WNL.39.6.789View ArticlePubMedGoogle Scholar
- Jinguji S, Yoshimura J, Nishiyama K, Aoki H, Nagasaki K, Natsumeda M, Yoneoka Y, Fukuda M, Fujii Y: Factors affecting functional outcomes in long-term survivors of intracranial germinomas: a 20-year experience in a single institution. J Neurosurg Pediatr 2013, 11: 454-463. 10.3171/2012.12.PEDS12336View ArticlePubMedGoogle Scholar
- Kiehna EN, Mulhern RK, Li C, Xiong X, Merchant TE: Changes in attentional performance of children and young adults with localized primary brain tumors after conformal radiation therapy. J Clin Oncol 2006, 24: 5283-5290. 10.1200/JCO.2005.03.8547View ArticlePubMedGoogle Scholar
- Surma-aho O, Niemelä M, Vilkki J, Kouri M, Brander A, Salonen O, Paetau A, Kallio M, Pyykkönen J, Jääskeläinen J: Adverse long-term effects of brain radiotherapy in adult low-grade glioma patients. Neurology 2001, 56: 1285-1290. 10.1212/WNL.56.10.1285View ArticlePubMedGoogle Scholar
- Deweer B, Pillon B, Pochon JB, Dubois B: Is the HM story only a “remote memory”? Some facts about hippocampus and memory in humans. Behav Brain Res 2001, 127: 209-224. 10.1016/S0166-4328(01)00366-7View ArticlePubMedGoogle Scholar
- Abayomi OK: Pathogenesis of cognitive decline following therapeutic irradiation for head and neck tumors. Acta Oncol 2002, 41: 346-350. 10.1080/028418602760169389View ArticlePubMedGoogle Scholar
- Monje ML, Mizumatsu S, Fike JR, Palmer TD: Irradiation induces neural precursor-cell dysfunction. Nat Med 2002, 8: 955-962. 10.1038/nm749View ArticlePubMedGoogle Scholar
- Yazlovitskaya EM, Edwards E, Thotala D, Fu A, Osusky KL, Whetsell WO Jr, Boone B, Shinohara ET, Hallahan DE: Lithium treatment prevents neurocognitive deficit resulting from cranial irradiation. Cancer Res 2006, 66: 11179-11186. 10.1158/0008-5472.CAN-06-2740View ArticlePubMedGoogle Scholar
- Tada E, Parent JM, Lowenstein DH, Fike JR: X-irradiation causes a prolonged reduction in cell proliferation in the dentate gyrus of adult rats. Neuroscience 2000, 99: 33-41. 10.1016/S0306-4522(00)00151-2View ArticlePubMedGoogle Scholar
- Nagai R, Tsunoda S, Asada H, Urabe N: Proliferating cell nuclear antigen positive cells in the hippocampal subgranular zone decline after irradiation in a rodent model. Neurol Res 2002, 24: 517-520. 10.1179/016164102101200285View ArticlePubMedGoogle Scholar
- Mizumatsu S, Monje ML, Morhardt DR, Rola R, Palmer TD, Fike JR: Extreme sensitivity of adult neurogenesis to low doses of X-irradiation. Cancer Res 2003, 63: 4021-4027.PubMedGoogle Scholar
- Greene-Schloesser D, Moore E, Robbins ME: Molecular pathways: radiation- induced cognitive impairment. Clin Cancer Res 2013, 19: 2294-2300. 10.1158/1078-0432.CCR-11-2903PubMed CentralView ArticlePubMedGoogle Scholar
- Rola R, Zou Y, Huang TT, Fishman K, Baure J, Rosi S, Milliken H, Limoli CL, Fike JR: Lack of extracellular superoxide dismutase (EC-SOD) in the microenvironment impacts radiation-induced changes in neurogenesis. Free Radic Biol Med 2007, 42: 1133-1145. 10.1016/j.freeradbiomed.2007.01.020PubMed CentralView ArticlePubMedGoogle Scholar
- Rodgers SP, Trevino M, Zawaski JA: Neurogenesis, exercise, and cognitive late effects of pediatric radiotherapy. Neural Plast 2013, 2013: 698528.PubMed CentralPubMedGoogle Scholar
- Ji JF, Ji SJ, Sun R, Li K, Zhang Y, Zhang LY, Tian Y: Forced running exercise attenuates hippocampal neurogenesis impairment and the neurocognitive deficits induced by whole-brain irradiation via the BDNF-mediated pathway. Biochem Biophys Res Commun 2014,443(2):646-651. 10.1016/j.bbrc.2013.12.031View ArticlePubMedGoogle Scholar
- Acharya MM, Christie LA, Hazel TG, Johe KK, Limoli CL: Transplantation of human fetal-derived neural stem cells improves cognitive function following cranial irradiation. Cell Transplant 2014,23(10):1255-1266. 10.3727/096368913X670200PubMed CentralView ArticlePubMedGoogle Scholar
- Manji HK, Moore GJ, Chen G: Lithium at 50: have the neuroprotective effects of this unique cation been overlooked? Biol Psychiatry 1999,46(7):929-940. 10.1016/S0006-3223(99)00165-1View ArticlePubMedGoogle Scholar
- Yang ES, Wang H, Jiang G, Nowsheen S, Fu A, Hallahan DE, Xia F: Lithium-mediated protection of hippocampal cells involves enhancement of DNA-PK-dependent repair in mice. J Clin Invest 2009, 119: 1124-1135. 10.1172/JCI34051PubMed CentralView ArticlePubMedGoogle Scholar
- Kraus RL, Pasieczny R, Lariosa-Willingham K, Turner MS, Jiang A, Trauger JW: Antioxidant properties of minocycline: neuroprotection in an oxidative stress assay and direct radical-scavenging activity. J Neurochem 2005, 94: 819-827. 10.1111/j.1471-4159.2005.03219.xView ArticlePubMedGoogle Scholar
- Plane JM, Shen Y, Pleasure DE, Deng W: Prospects for minocycline neuroprotection. Arch Neurol 2010, 67: 1442-1448.PubMed CentralView ArticlePubMedGoogle Scholar
- Zhang LY, Chen LS, Sun R, Ji SJ, Ding YY, Wu J, Tian Y: Effects of expression level of DNA repair-related genes involved in the NHEJ pathway on radiation-induced cognitive impairment. J Radiat Res 2013, 54: 235-242. 10.1093/jrr/rrs095PubMed CentralView ArticlePubMedGoogle Scholar
- Tian Y, Shi Z, Yang S, Chen Y, Bao S: Changes in myelin basic protein and demyelination in the rat brain within 3 months of single 2-, 10-, or 30-Gy whole-brain radiation treatments. J Neurosurg 2008, 109: 881-888. 10.3171/JNS/2008/109/11/0881View ArticlePubMedGoogle Scholar
- Garthe A, Kempermann G: An old test for new neurons: refining the Morris water maze to study the functional relevance of adult hippocampal neurogenesis. Front Neurosci 2013, 7: 63. 10.3389/fnins.2013.00063PubMed CentralView ArticlePubMedGoogle Scholar
- Czurkó A, Czéh B, Seress L, Nadel L, Bures J: Severe spatial navigation deficit in the Morris water maze after single high dose of neonatal x-ray irradiation in the rat. Proc Natl Acad Sci U S A 1997, 94: 2766-2771. 10.1073/pnas.94.6.2766PubMed CentralView ArticlePubMedGoogle Scholar
- Shors TJ, Miesegaes G, Beylin A, Zhao M, Rydel T, Gould E: Neurogenesis in the adult is involved in the formation of trace memories. Nature 2001,410(6826):372-376. 10.1038/35066584View ArticlePubMedGoogle Scholar
- Winocur G, Wojtowicz JM, Sekeres M, Snyder JS, Wang S: Inhibition of neurogenesis interferes with hippocampus-dependent memory function. Hippocampus 2006,16(3):296-304. 10.1002/hipo.20163View ArticlePubMedGoogle Scholar
- Jessberger S, Clark RE, Broadbent NJ, Clemenson GD Jr, Consiglio A, Lie DC, Squire LR, Gage FH: Dentate gyrus-specific knockdown of adult neurogenesis impairs spatial and object recognition memory in adult rats. Learn Mem 2009,16(2):147-154. 10.1101/lm.1172609PubMed CentralView ArticlePubMedGoogle Scholar
- Saxe MD, Battaglia F, Wang JW, Malleret G, David DJ, Monckton JE, Garcia AD, Sofroniew MV, Kandel ER, Santarelli L, Hen R, Drew MR: Ablation of hippocampal neurogenesis impairs contextual fear conditioning and synaptic plasticity in the dentate gyrus. Proc Natl Acad Sci U S A 2006,103(46):17501-17506. 10.1073/pnas.0607207103PubMed CentralView ArticlePubMedGoogle Scholar
- Madsen TM, Kristjansen PE, Bolwig TG, Wörtwein G: Arrested neuronal proliferation and impaired hippocampal function following fractionated brain irradiation in the adult rat. Neuroscience 2003,119(3):635-642. 10.1016/S0306-4522(03)00199-4View ArticlePubMedGoogle Scholar
- Kohman RA, Bhattacharya TK, Kilby C, Bucko P, Rhodes JS: Effects of minocycline on spatial learning, hippocampal neurogenesis and microglia in aged and adult mice. Behav Brain Res 2013, 242: 17-24. 10.1016/j.bbr.2012.12.032PubMed CentralView ArticlePubMedGoogle Scholar
- Ng SY, Semple BD, Morganti-Kossmann MC, Bye N: Attenuation of microglial activation with minocycline is not associated with changes in neurogenesis after focal traumatic brain injury in adult mice. J Neurotrauma 2012,29(7):1410-1425. 10.1089/neu.2011.2188View ArticlePubMedGoogle Scholar
- Mattei D, Djodari-Irani A, Hadar R, Pelz A, de Cossío LF, Goetz T, Matyash M, Kettenmann H, Winter C, Wolf SA: Minocycline rescues decrease in neurogenesis, increase in microglia cytokines and deficits in sensorimotor gating in an animal model of schizophrenia. Brain Behav Immun 2014, 38: 175-184. 10.1016/j.bbi.2014.01.019View ArticlePubMedGoogle Scholar
- Kong F, Chen S, Cheng Y, Ma L, Lu H, Zhang H, Hu W: Minocycline attenuates cognitive impairment induced by isoflurane anesthesia in aged rats. PLoS One 2013,8(4):e61385. 10.1371/journal.pone.0061385PubMed CentralView ArticlePubMedGoogle Scholar
- Ivanov VN, Hei TK: A role for TRAIL/TRAIL-R2 in radiation-induced apoptosis and radiation-induced bystander response of human neural stem cells. Apoptosis 2014, 19: 399-413. 10.1007/s10495-013-0925-4PubMed CentralView ArticlePubMedGoogle Scholar
- Jin WJ, Feng SW, Feng Z, Lu SM, Qi T, Qian YN: Minocycline improves postoperative cognitive impairment in aged mice by inhibiting astrocytic activation. Neuroreport 2014,25(1):1-6.PubMedGoogle Scholar
- Cai ZY, Yan Y, Chen R: Minocycline reduces astrocytic reactivation and neuroinflammation in the hippocampus of a vascular cognitive impairment rat model. Neurosci Bull 2010,26(1):28-36. 10.1007/s12264-010-0818-2View ArticlePubMedGoogle Scholar
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