Heterozygous mice expressing the human SCN1A R1648H GEFS+ mutation (Scn1a^RH/+) and heterozygous Scn1a knock-out mice (Scn1a^+/−) were generated as previously described (Yu et al., 2006; Martin et al., 2010) and maintained by backcrossing to the C57BL/6J and FVB backgrounds, respectively. Experiments were conducted at the N13 generation for Scn1a^RH/+ mutants and on a mixed FVB X C57BL/6J background for Scn1a^+/− mutants. Scn1a mutants and their respective wild-type (WT) littermates at P21-23 were used in the febrile seizure (FS) induction paradigm. Scn1a^RH/+ (3–5 months old) and Scn1a^+/− (4–6 weeks old) mutants and their respective age-matched WT littermates, as well as 6–8-week-old male CF1 mice (Charles River), were used for all other experiments. WT littermates were used as controls for all experiments to minimize variation due to differences in genetic background and rearing conditions. All mice were housed on a 12-h light/dark cycle, with food and water available ad libitum. All experiments were conducted during the light cycle prior to 4:00 p.m. and were performed in accordance with the guidelines of the Institutional Animal Care and Use Committee of Emory University. In experiments where both mutants and WT littermates were used, the experimenter was blinded to genotype. However, since Hup A administration results in visible mild side effects, it was not possible for the experimenter to be blinded to treatment.

Huperzine A (Hup A; Biscayne Pharmaceuticals) was suspended in a 10% solution of cyclodextrin (CD, 2-hydroxypropyl-β-cyclodextrin, Sigma-Aldrich) dissolved in sterile saline (0.9%). Hup A was administered via intraperitoneal (i.p.) injection (10 ml/kg) 1 h prior to seizure induction, based on previous studies that demonstrated maximum brain AChE inhibition at 1 h following Hup A administration (Tang et al., 1989). Control mice were handled similarly but were only administered vehicle (Veh, 10% CD).

Male CF1 mice (N = 3–4/dose) were administered either Hup A (doses based on a ¼ logarithmic scale: 0.10, 0.18, 0.32, 0.56, 1, or 1.8 mg/kg) or vehicle 1 h prior to sacrifice. The right hemisphere of the brain was used for quantification of protein (Pierce BCA Protein Assay, Thermo Scientific) and AChE activity using the standard spectrophotometric method (Ellman et al., 1961; Padilla et al., 1999).

Seizures were induced by the 6 Hz paradigm as previously described (Barton et al., 2001; Gilchrist et al., 2014). Briefly, 1 h prior to seizure induction, mice were administered either Hup A or vehicle (i.p.), and a topical anesthetic (0.5% tetracaine hydrochloride) was applied to the cornea. Each mouse was manually restrained during corneal stimulation (6 Hz, 0.2-ms pulse, 3 s) using a constant current device (ECT Unit 57800; Ugo Basile, Comerio, Italy), and then immediately placed in a clean cage for behavioral observations. Seizures were scored based on a modified Racine Scale (RS; Gilchrist et al., 2014): RS0, no abnormal behavior; RS1, immobile ≥ 3 s; RS2, forelimb clonus, paw waving; RS3, rearing and falling.

To determine the relationship between Hup A dose and susceptibility to 6 Hz-induced seizures, a ¼ logarithmic dose-response curve was generated following Hup A (0.10, 0.18, 0.32, 0.56, 1 mg/kg) or vehicle administration in male CF1 mice (N = 12). The 6 Hz paradigm was performed at a current of 44 mA, which was previously found to be twice the convulsive current at which 97% of CF1 mice seize (2xCC97; Barton et al., 2001). Over a 6-week experimental period, seizure induction was performed once per week on each mouse following the randomized administration of either vehicle or one of the Hup A doses, ensuring that all mice received each Hup A dose.

The effect of Hup A (1 mg/kg) on 6 Hz-induced seizures was evaluated further in a separate cohort of male CF1 mice (44 mA, N = 15). We also examined the effect of Hup A (0.5 and 1 mg/kg) on 6 Hz-induced seizures in male Scn1a^RH/+ (N = 9–12) and male Scn1a^+/− (N = 8–11) mice and their respective WT littermates. CF1 mice and Scn1a mutants and their WT littermates were randomized into 2 groups (0.5 mg/kg Hup A or Veh) over 2 trials (1 week apart). Mice that received Hup A during the first trial subsequently received vehicle during the second trial, and vice versa. The same experimental design was applied to separate cohorts of CF1 mice, Scn1a mutants and WT littermates using 1 mg/kg Hup A and vehicle. Scn1a^RH/+ and Scn1a^+/− mice were first tested at currents of 24 and 20 mA, respectively. The experiment was subsequently repeated in separate groups of mice at twice the initial current intensity (Scn1a^RH/+ = 48 mA, Scn1a^+/− = 40 mA).

To determine the contribution of different classes of neurotransmitter receptors to Hup A-mediated seizure protection, male CF1 mice (N = 5–12/group) were co-administered Hup A (1 mg/kg) and either a muscarinic receptor antagonist (scopolamine hydrobromide (SH), 30 mg/kg, Sigma-Aldrich), a GABA_A receptor antagonist (pentylenetetrazole, 25 mg/kg, Sigma-Aldrich), or a nicotinic receptor antagonist (bupropion hydrochloride (BH), 5 mg/kg, Sigma-Aldrich) 1 h prior to assessing the body temperature of each mouse and 6 Hz seizure induction (44 mA). All compounds were dissolved in sterile saline (0.9%). Similarly handled mice administered vehicle (cyclodextrin) or saline were used as controls.

Maximal electroshock seizures were induced as previously described (Swinyard, 1972). One hour prior to seizure induction, a topical anesthetic (0.5% tetracaine hydrochloride) was applied to the cornea, and Hup A (0.5 or 1 mg/kg) or vehicle was administered (i.p.) to male CF1 mice (N = 10/treatment), and male and female Scn1a^+/− and Scn1a^RH/+ mutants and their respective age- and sex-matched WT littermates (N = 5–13/genotype/treatment). Each mouse was manually restrained, subjected to corneal stimulation (60 Hz, 50 mA, 0.2 s; ECT Unit 57800 Ugo Basile, Comerio, Italy), and observed for the presence or absence of a seizure.

In a separate cohort of male CF1 mice (N = 6), body temperature was maintained at 37.5°C during the 1-h period following the administration of Hup A (1 mg/kg) prior to MES induction. Body temperature was maintained by the use of a rectal temperature probe connected to a heat lamp, with a thermostat set at 37.5°C.

Pentylenetetrazole (PTZ) seizures were induced as previously described (Loscher et al., 1991). Hup A (1 mg/kg) or vehicle was administered (i.p.) to male CF1 mice (N = 6/group) 1 h prior to subcutaneous PTZ injection (85 mg/kg). PTZ (Sigma-Aldrich) was dissolved in sterile saline (0.9%). Latencies to the first myoclonic jerk (MJ) and generalized tonic-clonic seizure (GTCS) were recorded over a 30-min observation period.

The effect of Hup A (1 mg/kg) or vehicle on seizures induced by the chemiconvulsant flurothyl (Prichahd et al., 1969; Dutton et al., 2011) was evaluated in male CF1 mice (N = 13–15/treatment). One hour prior to seizure induction, Hup A or vehicle was administered (i.p.) to each mouse. Next, each mouse was placed in a clear acrylic chamber and flurothyl (2,2,2-trifluroethylether; Sigma-Aldrich) was introduced at a constant rate of 20 μL/min. Latencies to the first MJ and generalized tonic-clonic seizure with hindlimb extension (GTCS-HLE) were recorded.

Susceptibility to hyperthermia-induced seizures were evaluated in male and female Scn1a^RH/+ (N = 4–6) and Scn1a^+/− (N = 9) mutants and their respective WT littermates (N = 3–7) at P21-23 as previously described (Oakley et al., 2009; Dutton et al., 2013). One hour prior to seizure induction, mice were administered Hup A (1 mg/kg) or vehicle and body temperature was maintained at 37.5°C. Hyperthermia seizure induction was then conducted (Dutton et al., 2013). Briefly, the body temperature of each mouse was elevated by 0.5°C every 2 min until the first GTCS or 42.5°C is reached. The temperature at which the seizure occurred was recorded.

The effect of chronic Hup A (0.5 and 1 mg/kg) administration on susceptibility to 6 Hz-induced seizures was first examined in male CF1 mice (N = 10/dose). On Day 0, all mice were administered vehicle (i.p.) 1 h prior to 6 Hz seizure induction (44 mA) to establish baseline seizure susceptibility. The mice were then divided into 2 cohorts based on the dose of Hup A administered. Cohort 1 mice received one injection per day of Hup A (0.5 mg/kg, i.p.) for 7 consecutive days and were subjected to 6 Hz seizure induction 1 h after Hup A administration on Day 7. Cohort 2 mice received Hup A (1 mg/kg, i.p.) for 12 consecutive days and were subjected to 6 Hz seizure induction 1 h after Hup A administration on Days 7 and 12. Cohort 2 mice then received Hup A (1.8 mg/kg, i.p.) for the next 5 consecutive days (Days 13–17), and 6 Hz seizures were induced 1 h after Hup A administration on Day 17. To determine the effect of chronic Hup A administration on AChE activity, separate groups of mice (N = 3/group) were administered Hup A (0.5 or 1 mg/kg) as described above for Cohorts 1 and 2, and AChE activity was quantified on Day 7 (to correspond with Cohort 1 mice) and Days 7 and 12 (to correspond with Cohort 2 mice).

We next determined the effect of chronic Hup A (1 mg/kg) administration on susceptibility to 6 Hz-induced seizures in male Scn1a^RH/+ mutants (N = 9). On Day 0, all mice were administered vehicle (i.p.) 1 h prior to seizure induction (24 mA) to establish baseline seizure susceptibility. The mice were then administered Hup A (i.p.) daily for 21 consecutive days and subjected to 6 Hz seizure induction on Days 7, 14, and 21. The mice were also subjected to 6 Hz seizure induction on Day 22 to determine whether Hup A conferred lasting protection.

A one-way repeated measures ANOVA (rANOVA) followed by the Dunn's multiple comparisons test (for non-parametric data) was used to compare Racine scores (RS) following 6 Hz seizure induction in CF1 mice, Scn1a mutants, and their respective WT littermates administered Hup A (0.10–1 mg/kg) or vehicle. A one-way ANOVA followed by the Holm-Šídák's multiple comparisons test was used to compare latencies to flurothyl-induced MJ and GTCS-HLE, percent AChE activity, and temperature in CF1 mice administered vehicle or Hup A (0.1–1.8 mg/kg). The chi-squared test was used to compare the percent of deaths between vehicle- and Hup-A treated mice following flurothyl seizure induction. An unpaired student's t-test was used to compare latencies to the MJ and GTCS following PTZ administration. A two-way ANOVA was used to compare the average temperature at seizure occurrence between Hup A- and vehicle-treated Scn1a mutants and their respective WT littermates during hyperthermia. A one-way rANOVA followed by the Dunn's multiple comparisons test was used to compare RS following 6 Hz seizure induction in CF1 and Scn1a^RH/+ mice during chronic Hup A administration. All data are presented as the mean ± SEM; p < 0.05 was considered statistically significant.

We first examined the relationship between Hup A dose (0.0–1.0 mg/kg) and resistance to seizures induced by the 6 Hz paradigm at 44 mA. The administration of Hup A was randomized with respect to the order in which each mouse received each dose of Hup A and vehicle. Each mouse was subjected to 6 Hz seizure induction once per week during the 6-week experimental period. Behavioral seizure responses were consistent for each Hup A dose, indicating that repeated seizure induction over the 6-week period did not influence seizure susceptibility or severity. Seizures were observed in all 12 vehicle-treated mice (1 RS1, 10 RS2, 1 RS3; Figure 1A), with most mice exhibiting forelimb clonus and paw waving. However, seizure occurrence and severity were significantly reduced following the administration of 0.56 and 1 mg/kg Hup A, with seizures observed in only 4/12 and 1/12 mice, respectively (Figure 1A). This robust Hup A-mediated protection against 6 Hz seizures was reproduced in a separate group of CF1 mice that were administered Hup A (1 mg/kg) or vehicle (N = 15/treatment, Figure 1B). As shown in Figure 1B, RS2 and RS3 seizures were observed in all vehicle-treated mice; however, 11/15 (74%) Hup A-treated CF1 mice were completely protected (RS0).

We also evaluated the effect of Hup A (0.1–1.8 mg/kg) on brain AChE activity 1 h after administration (Figure 1C). The two lowest Hup A doses (0.1 and 0.18 mg/kg) resulted in ~25% reduction in AChE activity when compared to vehicle-injected mice (p < 0.01). Hup A doses of 0.32–1.8 mg/kg resulted in comparable reductions of AChE activity (63–78%; Figure 2). Hup A doses of 0.56 or 1.0 mg/kg were selected for subsequent analyses based on the magnitude of their effect on AChE activity and the robust increase in seizure resistance associated with these doses.

The ability of Hup A to protect against MES-induced seizures was also examined in male CF1 mice. As expected, all vehicle-treated mice experienced a maximal seizure. In contrast, all CF1 mice treated with either 0.5 mg/kg or 1 mg/kg Hup A were protected. We next determined whether Hup A (1 mg/kg) was capable of increasing resistance to PTZ-induced seizures in CF1 mice (Figures 1D,E). Average latencies to the first PTZ-induced myoclonic jerk were significantly higher in Hup A-treated mice compared to vehicle-treated mice (p < 0.01, Figure 1D). Furthermore, only 2/6 Hup A-treated mice exhibited a GTCS, whereas all (6/6) vehicle-treated mice had a GTCS (Figure 1E). Of the mice that exhibited a GTCS, the latency to the initial GTCS was significantly higher in the Hup A-treated mice compared to mice administered vehicle (p < 0.01).

Contrary to the robust Hup A-mediated protection against 6 Hz, MES, and PTZ-induced seizures, average latencies to the flurothyl-induced MJ was significantly lower in Hup A-treated CF1 mice compared to vehicle-treated mice (Figure 1F, p < 0.01). Hup A administration did not significantly change the average latency to the GTCS-HLE (Figure 1G); however, 11/13 Hup A-treated mice died after the GTCS-HLE while all vehicle-treated mice survived.

Transient dose-dependent side effects (e.g., hypothermia, lethargy, fasiculations) were observed following acute Hup A administration. Since hypothermia has been shown to be neuroprotective and increases seizure resistance (Essman and Sudak, 1964), we examined whether it might contribute to Hup A-mediated seizure protection. To prevent the Hup A-induced hypothermia, we maintained the body temperature of male CF1 mice at 37.5°C during the 1-h interval between Hup A administration and seizure induction. Complete protection against MES-induced seizures was still observed in these mice, indicating that hypothermia does not contribute to Hup A-conferred seizure protection (data not shown).

We next examined whether Hup A was capable of reducing the occurrence or severity of 6 Hz-induced seizures in Scn1a^RH/+ and Scn1a^+/− mutants and their respective WT littermates. As previously described, mice were administered vehicle or Hup A (0.5 and 1 mg/kg) 1 h prior to seizure induction.

The ability of Hup A to protect against MES-induced seizures was examined in both sexes of Scn1a mutants and their respective WT littermates (Table 1). As expected, all vehicle-treated mice experienced a maximal seizure. Following the administration of 0.5 mg/kg Hup A, protection was observed in 5/9 male and 1/6 female Scn1a^RH/+ mutants and 10/11 male and 2/6 female WT littermates. Similarly, 5/10 male and 5/11 female Scn1a^+/− mutants and 8/9 male and 8/9 female WT littermates were protected. More robust seizure protection was observed among the mutant mice following the administration of 1 mg/kg Hup A regardless of sex and genotype. Specifically, 6/7 male and 6/8 female Scn1a^RH/+ mutants and all sex-matched WT littermates were protected. Similarly, all Hup A-treated male Scn1a^+/− mutants and 6/7 male WT littermates were protected. Protection was also observed in 6/9 Hup A-treated female Scn1a^+/− mutants and 9/10 female WT littermates.

The ability of Hup A to protect against hyperthermia-induced seizures was evaluated in Scn1a mutant mice and their respective WT littermates. All vehicle-treated Scn1a mutants exhibited a seizure. In contrast, WT littermates administered vehicle did not exhibit a seizure in this paradigm. Hup A-treated WT littermates responded similarly to the vehicle-treated WT mice. Although all Hup A-treated Scn1a^RH/+ and Scn1a^+/− mutant mice exhibited a seizure, the average temperature at seizure occurrence was significantly higher than the temperature at which the vehicle-treated mutants seized (Scn1a^RH/+, p < 0.01; Scn1a^+/−, p < 0.001; Figure 3).

Having established that acute Hup A administration confers robust seizure protection, we next investigated whether protection would be maintained during chronic Hup A delivery. We first examined the effect of daily Hup A administration (0.5 or 1 mg/kg) on susceptibility to 6 Hz-induced seizures in CF1 mice (Figures 4A,B). As previously observed, all mice exhibited RS2 seizures prior to initiating Hup A treatment (Day 0). Seizure response was next examined after 7 days of Hup A administration. In contrast to observations following acute treatment, no protection was observed in the mice that received 0.5 mg/kg Hup A (Figure 4A). At the higher dose of Hup A (1 mg/kg), robust protection was still seen after 7 days; however, protection was not observed on Day 12 (Figure 4B). To determine whether seizure protection in these mice could be restored by increasing the daily dose of Hup A, 1.8 mg/kg Hup A was administered for the next 5 consecutive days (Days 13–17). On Day 13, we observed a statistically significant increase in seizure protection when compared to Day 0; however, protection was not observed on Day 17.

Chronic Hup A administration did not alter its effect on AChE activity, with approximately a 60% reduction observed after 7 days of 0.5 mg/kg and a 70% reduction after 7 and 12 days of 1 mg/kg (Figure 4C). Furthermore, the transient side effects, including fasiculations, hypothermia, and lethargy, diminished with continued administration. We also examined the effect of chronic Hup A administration (1 mg/kg) on susceptibility to 6 Hz-induced seizures in Scn1a^RH/+ mice. At baseline (Day 0), all vehicle-treated mutants (9/9) experienced a severe seizure (6 RS2, 3 RS3, Figure 4D). However, we observed complete protection against 6 Hz-induced seizures after 7, 14, and 21 consecutive days of Hup A administration (p < 0.01). To determine whether seizure protection would be maintained after cessation of Hup A administration, 6 Hz seizures were induced 24 h after the last Hup A injection (Day 22); however, we found no significant difference between the seizure responses on Days 0 and 22, indicating a lack of maintained seizure protection.

To gain further insight into the mechanism of action of Hup A, we examined the effect of blocking muscarinic receptors, nicotinic receptors, or GABA_A receptors on Hup A-conferred resistance to 6 Hz seizures in CF1 mice. Mice were co-administered Hup A (1 mg/kg) and each antagonist 1 h prior to seizure induction, and seizure response was compared to control mice that were injected with vehicle plus saline, vehicle plus antagonist, and Hup A plus saline (Figure 5). Seizure responses were comparable between control mice administered vehicle plus saline and vehicle plus each antagonist, confirming that the doses of the antagonists used did not alter seizure response (Figure 5).

Block of central muscarinic receptors was achieved by injection of the muscarinic receptor antagonist, scopolamine hydrobromide (SH; Figure 5A). All control mice that received vehicle and saline or vehicle and SH exhibited RS2 seizures. These results also demonstrate that SH alone does not worsen or ameliorate the behavioral seizure response. In contrast to the seizure protection observed in the Hup A plus saline group, all mice co-administered Hup A and SH exhibited RS2 seizures, demonstrating a role for muscarinic receptors in Hup A-mediated seizure protection. The seizure response of mice administered Hup A and the GABA_A receptor antagonist PTZ were comparable to control mice that received vehicle and saline or vehicle plus PTZ, indicating that GABA_A receptors also contribute to Hup A-mediated seizure protection (Figure 5C). However, 4/12 mice administered Hup A plus PTZ did not exhibit a seizure and 2/12 mice had mild seizures (RS1), raising the possibility that blocking GABA_A receptors only partially affects Hup A activity (Figure 5C). In contrast, the nicotinic receptor antagonist bupropion hydrochloride (BH) had no effect on Hup A activity, as demonstrated by the comparable seizure response of the Hup A plus saline and Hup A plus BH groups (Figure 5E).

To determine whether these receptors were involved in the Hup A-induced hypothermia, we also measured the body temperature of the mice 1 h after drug administration. The average body temperature of mice administered Hup A plus SH was comparable to the control mice and was significantly higher than the Hup A plus saline group (Figure 5B). Although the higher body temperature observed in mice co-administered Hup A and BH was statistically different from the Hup A plus saline group (p < 0.05), the average body temperature in the presence of BH was still significantly lower than the control mice (Figure 5F). Average body temperature of mice co-administered Hup A and PTZ was comparable to mice given Hup A and saline, suggesting that GABA_A receptors are not involved in the Hup A-mediated hypothermia (p < 0.0001, Figure 5D).

The 6 Hz seizure induction paradigm uses a 3-s, low-frequency (6 Hz) current to produce a seizure that is less intense and more focal compared to seizures generated by MES and PTZ (Brown et al., 1953). In conjunction with c-Fos immunohistochemistry, Barton et al. (2001) found that different regions of the brain could be activated by varying the intensity of the current used in the 6 Hz paradigm. Lower intensities (22 and 32 mA; CC97 and 1.5xCC97 for CF1 mice, respectively) activate the amygdala, cortices, and entorhinal cortex, while a higher current (44 mA; 2xCC97) activates the dentate gyrus of the hippocampus. Based on these findings, the 6 Hz seizure induction paradigm has been used as a model of therapy-resistant limbic seizures (Barton et al., 2001).

We found that 0.56 and 1 mg/kg of Hup A provided robust protection against 6 Hz-induced seizures (44 mA) in CF1 mice. Consistent with these results, we found that both Hup A doses also provided seizure protection in the Scn1a mutant mice. Interestingly, robust seizure protection was still achieved in Scn1a mutants when the current was doubled (48 mA for Scn1a^RH/+ and 40 mA for Scn1a^+/−), suggesting that Hup A might also provide protection against spontaneous seizures in DS that may initiate in the hippocampus (Liautard et al., 2013).

Daily administration of Hup A (1 mg/kg) provided protection against 6 Hz-induced seizures in CF1 mice for 7–12 days. More importantly, we demonstrated in the Scn1a^RH/+ mutants that Hup A could be provided daily for at least 21 days without loss of seizure protection. However, we did not observe protection 24 h after cessation of treatment. Two potential reasons for the observed differences in the effect of chronic Hup A administration between the CF1 mice and the Scn1a^RH/+ mutants are: (1) the different genetic backgrounds of each strain and (2) the predicted increase in neuronal inhibition attributable to Hup A might confer greater seizure protection in the mutants due to the effect of the Scn1a mutation on the excitability of inhibitory interneurons. These results make Hup A an attractive therapeutic option for epilepsy since chronic treatment is often necessary.

The MES paradigm uses a high-frequency current of short duration (60 Hz, 50 mA, 0.2 ms) to produce a seizure that can spread throughout the brain (Toman, 1951) as reflected in c-Fos expression in distal structures, such as the midbrain and brainstem (Barton et al., 2001). Drugs that can inhibit seizure propagation are highly effective in the MES paradigm (Woodbury and Esplin, 1959). Furthermore, compounds that are effective against MES-induced seizures are found to clinically block or mitigate generalized tonic-clonic seizures (GTCSs; White et al., 1995). Valproate and topiramate, two AEDs currently used in the treatment of DS (Shi et al., 2015), also protect against MES-induced seizures. Our findings that Hup A protects against MES-induced seizures in Scn1a mutants suggest that it may provide protection by blocking seizure propagation.

Similar to 6 Hz and MES, we observed robust protection against PTZ-induced seizures in CF1 mice. This was reflected by the absence of a GTCS in 4 of 6 Hup A-treated mice and an increase in average latencies to the MJ and GTCS (in the mice that did exhibit a GTCS). These results are consistent with the recent findings by Gersner et al. (2015), where Hup A (0.6 mg/kg) was found to protect against PTZ-induced seizures in rats. Similar to our results, a significantly lower number of Hup A-treated rats (only 30%) exhibited a GTCS compared to saline-treated rats (~75%). PTZ seizure induction is routinely used for screening potential anticonvulsants in part because protection against PTZ-induced seizures is predictive of efficacy in treating absence epilepsy (Krall et al., 1978).

In contrast, following flurothyl exposure, we observed a decrease in the average latency to the MJ and higher mortality following the GTCS-HLE in Hup A-treated mice. Seizure behavior and c-Fos immunoreactivity patterns have been found to be similar following flurothyl and PTZ seizure induction (Jensen et al., 1993), which are both mediated, at least in part, by inhibition of GABA_A receptors. The ability of Hup A to provide protection against PTZ but not flurothyl-induced seizures suggests the contribution of a non-GABAergic component to the mechanism of action of flurothyl. Finally, it is possible, since flurothyl is inhaled, there may be peripheral effects elicited by both flurothyl and Hup A that, when combined, worsens the seizure phenotype.

Infants with SCN1A mutations often experience severe and prolonged febrile seizures (FSs) that can have a negative impact on long-term prognosis (Wolff et al., 2006; Akiyama et al., 2010). Currently, there are no routine clinical interventions that can protect against early-life FSs. We and others have demonstrated increased susceptibility to hyperthermia-induced seizures in Scn1a mutant mice (Oakley et al., 2009; Dutton et al., 2013). Although the mechanism underlying febrile seizure generation is not fully understood, it has been demonstrated that febrile seizures originate from the limbic region of the brain, notably the amygdala and hippocampus (Dube et al., 2000; Brewster et al., 2002). Consistent with the robust Hup A-mediated protection against 6 Hz-induced seizures (a model of limbic epilepsy), we observed a significant increase in the temperature at which hyperthermia-induced seizures occurred in Hup A-treated Scn1a mutant mice. Cao and others have suggested that the temperature at seizure occurrence is a good measure of drug efficacy as this index is reproducible within the same mouse (Cao et al., 2012). Other drugs, such as stiripentol, that have demonstrated clinical efficacy in the treatment of SCN1A-derived epilepsy have also been shown to increase resistance to hyperthermia-induced seizures in Scn1a rodent models (Hayashi et al., 2011; Cao et al., 2012).

Hup A-mediated inhibition of brain AChE is known to be dose dependent and comparable across routes of administration. Tang et al. (1989) found that Hup A (0.5–1 mg/kg) provided the greatest inhibition of AChE throughout the entire brain (up to 42%), with the fewest side effects. Laganiere et al. (1991) found that 0.5 mg/kg Hup A significantly reduced AChE activity in the hippocampus, striatum, and septum (20–45%), whereas 0.1 mg/kg Hup A only slightly reduced AChE activity in these brain regions. In Rhesus monkeys, Myers et al. (2010) also found that Hup A (5–40 μg/kg) resulted in a dose-dependent inhibition of AChE activity (31–74%) without adverse cognitive effects. Although we found that Hup A doses of 0.32–1 mg/kg produced similar reductions in AChE activity, which may indicate a floor effect on AChE activity, more robust seizure protection was observed with 0.56 and 1 mg/kg Hup A. We also observed similar reductions in AChE activity regardless of whether Hup A was administered acutely or chronically (Figure 5C). These findings suggest that Hup A-mediated seizure protection is not dependent solely on the level of AChE activity. In addition, previous studies demonstrated that Hup A inhibition of AChE occurs significantly faster than the corresponding increases in acetylcholine (Tang et al., 1989).

Recently, focal seizures (as a result of hippocampal stimulation) were found to result in decreased subcortical cholinergic neurotransmission both during and after a seizure (Motelow et al., 2015). Decreased acetylcholine levels in the thalamus have also been noted in partial seizures and slow-wave sleep (Williams et al., 1994). Our findings that Hup A protects against 6 Hz-induced seizures, a model of focal limbic seizures, and the noted decreased cholinergic neurotransmission in focal seizures (Motelow et al., 2015), suggest that Hup A may also be efficacious in the treatment of TLE.

Elevated body temperature is known to induce epileptic activity and seizures in animals, while hypothermia (29–34.5°C) has been shown to be anticonvulsant (Essman and Sudak, 1964). We observed that upon acute administration of Hup A, mice displayed transient side effects, including hypothermia. To determine whether Hup A-induced hypothermia contributes to seizure protection, we held the body temperature of mice at 37.5°C for the 1 h interval between Hup A administration and MES induction. Under these conditions, we found that Hup A-induced hypothermia does not contribute to seizure protection.

To evaluate potential neurotransmitter receptors that may be involved in Hup A-mediated seizure protection, we co-administered Hup A and receptor antagonists 1 h prior to 6 Hz seizure induction. Atropine, a competitive muscarinic receptor antagonist that targets receptors in both the central and peripheral nervous systems, has been demonstrated (at 30 mg/kg) to block the protective effects of Hup A in the 6 Hz paradigm (Bialer et al., 2015). However, Gersner et al. (2015) found that co-administration of atropine (30 mg/kg) and Hup A did not block the magnitude of paired-pulse inhibition, suggesting that muscarinic receptors are not involved in Hup A-mediated cortical interneuron activation. We found that the co-administration of scopolamine hydrobromide, a centrally acting muscarinic receptor antagonist, blocked Hup A-mediated protection against 6 Hz-induced seizures. We also found that the co-administration of PTZ, a GABA_A receptor antagonist, also partially blocks Hup A-mediated protection in the 6 Hz paradigm. However, the co-administration of a nicotinic receptor antagonist did not block Hup A-mediated seizure protection. These results suggest that Hup A may provide seizure protection through the activation of several pathways, including the muscarinic and GABA_A receptors.

Increases in acetylcholine have been shown to decrease body temperature in both humans (Cushing, 1931) and rodents (Everett, 1956) by acting upon interneurons in the hypothalamic thermoregulatory zone. Our results demonstrate that Hup A-induced hypothermia involves both muscarinic and nicotinic cholinergic receptors. Co-administration of Hup A and the muscarinic receptor antagonist, SH, resulted in the maintenance of normal body temperature. Although co-administration of the nicotinic receptor antagonist, BH, partially prevented the decrease in body temperature observed in Hup A plus saline-injected mice, the average body temperature of Hup A plus BH mice was still significantly lower than control mice. Our findings suggest that Hup A-induced hypothermia is mediated primarily by the muscarinic cholinergic receptor.

SC has a financial interest in Biscayne Pharmaceuticals, which is the holder of all commercial rights to Huperzine A. SS is an inventor on a patent for the use of Huperzine A for the treatment of epilepsy, which is licensed by Harvard Medical School to Biscayne Pharmaceuticals, in which he holds less than 5% equity and for which he serves as chair of the scientific advisory board. The other authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.