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Nimodipine treatment does not benefit juvenile ferrets with kaolin-induced hydrocephalus
Fluids and Barriers of the CNSvolume 15, Article number: 14 (2018)
Prior research on 3-week hydrocephalic rats showed that behavioral deficits and white matter damage could be reduced by treatment with Ca2+ channel blocker nimodipine. We hypothesized that treatment with nimodipine would be also beneficial to young ferrets with kaolin-induced hydrocephalus. Hydrocephalus was induced at 14 days of age and animals were treated either with vehicle, low dose nimodipine (3.2 mg/kg/day), or high dose nimodipine (16 mg/kg/day) for 2 weeks from 38 to 52 days age. Hydrocephalic ferrets developed progressive ventriculomegaly, behavioral changes, and in some cases cortical blindness. These changes were not ameliorated by nimodipine. Histological examination showed damage in periventricular white matter, corpus callosum thinning, axonal damage, reactive astroglial changes, and suppressed cell proliferation compared to non-hydrocephalic controls. Treatment with nimodipine was not beneficial for any of the pathological changes mentioned above; only low dose nimodipine treatment was associated with normalized content of glial fibrillary acidic protein, despite larger ventricles. We conclude that young hydrocephalic ferrets experience behavioral impairments and structural brain damage that are not consistently improved by intermittent nimodipine treatment. Continuous delivery should be considered in further preclinical studies.
Brain damage induced by hydrocephalus is multifactorial commencing with mechanical factors and local ischemia that result in destruction of periventricular axons . The gradual nature of damage means that there might be an opportunity for an early pharmacologic intervention to reduce the damage prior to definitive treatment such as cerebrospinal fluid (CSF) shunting . Nimodipine is a lipophilic antagonist of voltage-dependent selective dihydropyridine type (L-type) calcium (Ca2+) channels . It can cross the blood–brain-barrier  and in animals has been shown to cause cerebral vasodilatation . However, one small clinical study on eight adults with normal pressure hydrocephalus showed that nimodipine treatment reduced the arterial blood pressure, had no effect calculated on cerebral blood flow, and was associated with a slight increase in intracranial pressure during a 4 h monitoring period . We previously showed that 3-week old rats with kaolin-induced hydrocephalus benefited behaviorally and structurally by treatment with continuous parenteral administration of nimodipine for 2 weeks . In preclinical trials it is necessary to demonstrate the utility and safety of this treatment in a larger species with gyrencephalic brain . Therefore, this study was aimed to determine if nimodipine would benefit juvenile ferrets .
Thirty-five pigmented sable ferret kits (n = 26 males and n = 9 females) were obtained from Marshall Farms (North Rose, NY) at postnatal age 7–9 days (P7–P9) among 6 l along with their mothers. All animals were treated humanely based on the Canadian Council on Animal Care guidelines. The University of Manitoba animal ethics committee approved the experiment (protocol #15-076). The methods of animal handling, anesthesia, induction of hydrocephalus, magnetic resonance (MR) imaging, behavioral testing, euthanasia, biochemical analyses, and histological analyses were all as previously described in detail [8, 9]. Below we highlight the experimental timing, drug utilization, and any additions to prior work.
Hydrocephalus was induced in anesthetized (3.0% isoflurane) ferrets with percutaneous intracisternal injection of kaolin or sham (saline) at P14 (weight 44–81 g; 5–6 kits/l; total n = 35). Subcutaneous (sc) injections of buprenorphine (0.03 mg/kg) and sterile 0.45% saline were given every 8–12 h over 2 days to reduce pain and dehydration. T2-weighted MR images of brain were obtained using a 7 T Bruker Biospec/3 MR scanner (Karlsruhe, Germany). MR imaging at 2 days post kaolin (P16) ensured that hydrocephalus had been successfully induced; in the case of failures, an additional dose of kaolin was administered. Nine kits died after kaolin injections leaving 26 that underwent MR imaging 15 days after kaolin (at P29). Using the lateral ventricle to brain size ratios, ferrets were stratified and assigned list wise to vehicle (0 mg/kg/day), low dose nimodipine (3.2 mg/kg/day), and high dose nimodipine (16 mg/kg/day) treatment groups. The final set of MR images was obtained on P52, after 2 weeks drug therapy, no more than 24 h before sacrifice.
Stock solutions of nimodipine (Sigma, St. Louis, MO) were prepared in 40% dimethyl sulfoxide (DMSO; Fisher Scientific, Nepean ON), 10% ethanol, 50% 0.9% NaCl in distilled water and stored at 4 °C. The solutions of various nimodipine concentrations along with a sham vehicle were labeled A, B, and C. Treatments were administered blindly based upon a subcutaneous injection volume to body weight formula of 1 ml/100 g twice per day (approximately at 08.00 and 18.00 h). The nimodipine dose was either 3.2 mg/kg/day (low) or 16 mg/kg/day (high). These doses were based on the previous rodent experiment wherein nimodipine 8–13 mg/kg/day was found to be protective and 20 mg/kg/day exhibited mild toxicity . Note that the doses are not entirely comparable owing to differences in administration routes (osmotic minipumps in rats). Treatments were started 15–17 days post-kaolin at P29–P31 (n = 9 vehicle; n = 9 low dose; n = 8 high dose). Treatments were temporarily halted after 2 days because several ferrets suffered lethargy and rapid weight loss. We suspected an adverse reaction to the vehicle; therefore, the drug solutions were reformulated in half the volume of vehicle. Drug administration resumed at P38, which allowed a 14-day treatment period.
Behavioral testing commenced at P9–P11 and continued three times weekly until P48–P50. Activity was measured in an enclosed square container (44 × 43 × 29 cm) with infrared light beam sensors to record vertical, ambulatory, and total movements (Opto-Varimex 3; Columbus Instruments International Corp., Columbus, OH, USA). Open field activity was video recorded in a transparent enclosure (75 × 75 × 45 cm) for quantitative assessment of ambulation. Vision was tested when the ferrets started to open their eyes (P36) using a foam ball (5 cm diameter, painted red) attached to the end of a metal stick. The ball was introduced in two different manners. First, it was held at the side of the ferret and waved (approximately 2 cm amplitude) until the animal turned its head toward the ball. Second, the ball was placed in front of the kit then moved slowly to see if the ferrets would track the ball. Outcomes were reported semi-quantitatively with three categories: normal visual response (0), abnormal visual response (1), and no visual response (2).
Ferrets were euthanized at P52, within 24 h of the final MR imaging, using isoflurane anesthesia (5%) followed by exsanguination by transcardiac perfusion with 0.1 M phosphate buffered saline. The brains were excised, weighed, and cut in the parasagittal plane. Samples of dorsal frontal cerebrum and dorsal parietal cerebrum were frozen. The left hemisphere was immersion fixed in cold 10% buffered formalin for 2–3 weeks, sliced in the coronal plane, dehydrated, and embedded in paraffin. Paraffin blocks were sectioned (6 μm thickness) for staining with hematoxylin + eosin and with solochrome cyanin + eosin for examination of myelin. Corpus callosum thickness was measured at the midline and above the lateral angle of the lateral ventricle. Immunostains included: rabbit polyclonal anti-glial fibrillary acidic protein (GFAP; 1:10,000 dilution; DAKO Z0334; Glostrup, Denmark) to label astrocytes; rabbit polyclonal anti-Ki67 (1:250 dilution; Novocastra NCL-Ki67p; Newcastle upon Tyne, UK) to label proliferating cells in the subventricular zone (SVZ); and rabbit polyclonal anti-amyloid-β precursor protein (APP; 1:3000 dilution; Invitrogen 36-6900; Camarillo, CA, USA) to identify damaged axons. GFAP content was measured in frozen frontal lobe samples using ELISA as previously described in detail .
Quantitative data (mean ± standard error of the mean) were analyzed to ensure a normal distribution, and p values ≤ 0.05 were deemed statistically significant. Statistical analyses were performed for the weight, ventricle size, and behavioral tests at multiple time points. Weights, behavioral test, ventricle size, histological, and ELISA data were analyzed using analysis of variance (ANOVA) and two-tailed t-tests (SPSS 19.0 software program). Vision data were analyzed using Chi square. Histological cell counts, corpus callosum thickness, and GFAP ELISA analyses were conducted only on ferrets that completed the 2-week drug trial (n = 17).
Thirty-three ferrets were injected with kaolin and two with saline. Nine died within 2 days of kaolin injection and nine more died as a complication of the initial vehicle solvent formulation. Table 1 shows the initial sample size (“Intent to treat”) and the final sample size after accounting for all mortality. Kaplan–Meier survival analysis performed on hydrocephalic ferrets during the 2-week treatment period showed no significant difference in survival between sham, low dose, and high dose nimodipine-treated groups (p = 0.443 to p = 0.532). On MR images, mild ventriculomegaly was apparent by 2 days after kaolin injections, particularly involving the lateral ventricles. At 14 days post-kaolin, ventricular expansion was mild to severe (Fig. 1; p < 0.005, t tests). All three hydrocephalic treatment groups showed further ventricular enlargement of the lateral and fourth ventricles during the treatment period (to P52). However, the enlargement did not differ between groups (p > 0.05, ANOVA; Table 1).
Hydrocephalic and non-hydrocephalic ferrets reached motor and behavioral developmental milestones at approximately the same time. All were crawling by P27–P29 and started walking between P34 and 37 . Hydrocephalic ferrets tended to display higher activity scores during the first week after kaolin injections. During the second week after kaolin (P24–26), non-hydrocephalic ferrets showed more ambulation and activity than hydrocephalic ferrets (p < 0.010). There were no consistent behavioral differences between the three hydrocephalic groups during the drug trial phase (Table 1). Four hydrocephalic ferrets exhibited severe visual impairments during the last week of the study (Table 1); they tended to circle continuously in their enclosures.
Histologic evaluation of the hydrocephalic ferrets showed that ventriculomegaly was accompanied by compression of periventricular white matter (Fig. 2), focal fraying of the corpus callosum, and reduced cellularity at the dorsolateral angle of the frontal horn. Where white matter was intact, the intensity of myelin staining was similar in hydrocephalic and non-hydrocephalic ferrets. However, damaged periventricular white matter regions displayed reduced myelin staining (Fig. 2). The corpus callosum was thinner in hydrocephalic animals than in non-hydrocephalic animals (p = 0.005, t test), but there were no statistically significant differences between the hydrocephalic treatment groups (Table 1). In the severely hydrocephalic ferrets, particularly those with visual impairment, damaged axons with APP immunoreactivity were abundant in the parietal-occipital white matter (not shown).
Non-hydrocephalic ferrets have proliferating cells demonstrable by Ki67 immunoreactivity in the residual SVZ at the dorsolateral angle of the frontal horn (Fig. 3). Untreated and high dose nimodipine-treated hydrocephalic ferrets had a thinner SVZ and fewer Ki67 positive cells compared to controls (Table 1). Hydrocephalic ferrets had GFAP-immunoreactive hypertrophic reactive astrocytes in the white matter; there were no obvious differences between the hydrocephalic drug treatment groups (Fig. 3). ELISA of frontal lobe homogenates showed elevated GFAP content in untreated and high dose nimodipine hydrocephalic ferrets compared to non-hydrocephalic controls, but the difference was not significant (Table 1; p = 0.676, t test).
Nimodipine was previously shown to have mild neuroprotective effects when administered for 2 weeks to juvenile rats with kaolin induced experimental hydrocephalus . However, this study revealed that comparable doses in young hydrocephalic ferrets did not offer any consistent behavioral, histological, or biochemical improvements. Although there was normalization of GFAP content and Ki67 counts in ferrets treated with low dose nimodipine, that group had the greatest expansion of the ventricles during the drug administration phase.
Why did the nimodipine treatment, as well as a magnesium sulfate treatment , fail in ferrets when they had been modestly protective in hydrocephalic rats? It could be a species-specific matter or possibly related to the degree of brain maturation. Hydrocephalic rats were treated from 5 to 7 weeks age, which in relative terms of cerebral myelination is slightly more mature than the ferrets studied here (http://translatingtime.org/ ) [8, 11]. There is also a possibility that the treatment was applied late to mitigate severe damage; we had too few cases to correlate ventricle size with magnitude of treatment effect.
It is also possible that the mode of drug delivery played a role. Hydrocephalic rats received a continuous infusion of nimodipine via osmotic minipumps. In this case there was a concern about maternal rejection , therefore we applied the drug by subcutaneous injections. In dogs (which along with ferrets are of the Caniformia suborder within the order Carnivora) the elimination half-life of nimodipine after intravenous injection and after ~ 5 mg/kg oral dose is ~ 1.8 h . Therefore, it is likely that the ferrets’ brains were not exposed continuously to nimodipine. An implantable delivery system for nimodipine treatment of subarachnoid hemorrhage has been developed , but it is prohibitively expensive. Sustained release oral preparations are also under development .
The most surprising complication in this experiment was initial mortality attributable to the vehicle mixture of DMSO and ethanol, which was identical to that used in our rat experiment . DMSO is generally considered to be safe . However, chronic ocular toxicity is greater in dogs than in rats  and it is likely that metabolism of DMSO differs between very young ferrets and adults .
In summary, 2-week intermittent subcutaneous dosing of nimodipine to hydrocephalic ferrets from age 38 to 52 days was not shown to be beneficial. Timing, administration route, and dosage may have all contributed to the ineffective therapeutic outcome. While we do not absolutely reject the proposal that nimodipine can modulate damage in immature brains with hydrocephalus, this experiment shows that the window of opportunity might be narrow. More robust preclinical studies with continuous delivery or administration of long-acting nimodipine are required before considering a clinical trial in humans.
analysis of variance
cerebral blood flow
enzyme linked immunosorbent assay
glial fibrillary acidic protein
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DDC carried out the drug administration, behavioral tests, tissue dissections, histology, ELISAs, statistical analyses, and drafted the manuscript. AB assisted in the drug administration, behavioral tests, and MR imaging. XM assisted in the induction of hydrocephalus, drug administration, behavioral tasks, MR imaging, and performed the ELISAs. MRD conceived the study including its design and coordination, carried out the hydrocephalus induction, and guided writing of the manuscript. All authors read and approved the final manuscript.
The authors thank Dr. Richard Buist for conducting the MR imaging.
The authors declare that they have no competing interests.
Availability of data
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Consent for publication
Ethics approval and consent to participate
University of Manitoba animal ethics committee protocol #15-076.
This work was funded by a grant from the Hydrocephalus Association to Dr. Del Bigio. Dr. Del Bigio holds the Canada Research Chair in Developmental Neuropathology. Mr. Baker received a stipend from the B.Sc. (Med.) program of the University of Manitoba.
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