Abstract
The medial septum/diagonal band (MSDB), which gives rise to the septohippocampal pathway, is a critical locus for the mnemonic effects of muscarinic drugs. Infusion of muscarinic cholinergic agonists into the MSDB enhance learning and memory processes both in young and aged rats and produce a continuous theta rhythm in the hippocampus. Intraseptal muscarinic agonists also alleviate the amnesic syndrome produced by systemic administration of muscarinic receptor antagonists. It has been presumed, but not proven, that the cellular mechanisms underlying the effects of muscarinic agonists in the MSDB involve an excitation of septohippocampal cholinergic neurons and a subsequent increase in acetylcholine (ACh) release in the hippocampus. Using a novel fluorescent labeling technique to selectively visualize live septohippocampal cholinergic neurons in rat brain slices, we have found that muscarinic agonists do not excite septohippocampal cholinergic neurons, instead they inhibit a subpopulation of cholinergic neurons. In contrast, unlabeled neurons, confirmed to be noncholinergic, septohippocampal GABA-type neurons using retrograde marking and double-labeling techniques, are profoundly excited by muscarine. Thus, the cognition-enhancing effects of muscarinic drugs in the MSDB cannot be attributed to an increase in hippocampal ACh release. Instead, disinhibitory mechanisms, caused by increased impulse flow in the septohippocampal GABAergic pathway, may underlie the cognition-enhancing effects of muscarinic agonists.
Basic and clinical studies have long recognized the importance of cholinergic mechanisms in cognitive functioning (Givens and Sarter, 1997), and drugs that increase synaptic acetylcholine levels are currently the most used for the treatment of cognitive deficits associated with CNS disorders such as Alzheimer's disease, albeit, with limited effectiveness (Benzi and Moretti, 1998). The septohippocampal (SH) pathway, which originates in the medial septum/diagonal band (MSDB) and shows progressive degeneration in Alzheimer's disease (Whitehouse et al., 1982), has specifically been implicated in cognitive mechanisms. Lesions of the fimbria-fornix, which conveys SH cholinergic (Lewis and Shute, 1967) and GABAergic fibers to the hippocampus (Kohler et al., 1984; Freund, 1989), interfere both with learning and memory tasks and with generation of the theta rhythm in rats (Brito and Brito, 1990). These deficits can be attenuated by grafting ACh-producing cells to the hippocampus (Dunnett et al., 1982; Dickinson-Anson et al., 1998).
Cholinergic mechanisms operating within the MSDB are also critical for learning and memory. Thus, infusions of muscarinic agonists directly into the MSDB elicit continuous hippocampal theta (Monmaur and Breton, 1991; Lawson and Bland, 1993) and facilitate learning and memory-related behaviors both in young (Givens and Olton, 1990) and aged rats (Markowska et al., 1995). Intraseptal infusions of muscarinic agonists can also alleviate systemic scopolamine-induced amnesia, suggesting that the MSDB is a critical locus for the mnemonic effects of muscarinic drugs (Givens and Olton, 1995).
In general, it is assumed that improvements in SH pathway-related learning and memory tasks occurs as a result of an increase in hippocampal ACh release (Monmaur and Breton, 1991; Givens and Olton, 1994, 1995; Apartis et al., 1998; Bland and Oddie, 1998;Dickinson-Anson et al., 1998). As such, it has been presumed that the memory-enhancing effects of intraseptal-muscarinic agonists occur because of increased firing of SH cholinergic neurons (Markowska et al., 1995; Givens and Sarter, 1997). These assumptions have been based on earlier studies that reported a muscarinic receptor-mediated increase in firing of SH neurons (Dutar et al., 1983; Lamour et al., 1984), which lead to the hypothesis that ACh, via muscarinic receptors, has a positive feedback effect on SH cholinergic neurons (Dutar et al., 1983; Lamour et al., 1984; Segal, 1986). However, the SH neurons recorded from in these studies were presumed but not proven to be cholinergic. A small sample of cholinergic-type MSDB neurons (n = 3), classified using electrophysiological characteristics, were found to be inhibited by muscarine (Serafin et al., 1996). Additional effects of muscarine, such as a block of late afterhyperpolarization (Sim and Griffith, 1991) and decrease in glutamate transmission (Sim and Griffith, 1996) have also been reported in unidentified basal forebrain neurons. Effects of muscarinic agonists on identified septohippocampal cholinergic neurons have not been investigated.
In the present study, we used a novel fluorescent marker, Cy3–192IgG, to selectively label live rat SH cholinergic neurons and studied their response to cholinergic drugs using extracellular and whole-cell recordings in brain slices. Cy3–192IgG is prepared by conjugating the inert fluorochrome, Cy3, with an antibody against the p75 neurotrophin receptor. When injected intraventricularly, Cy3–192IgG retrogradely labels only p75 receptor-expressing neurons (Hartig et al., 1998), which in the MSDB are exclusively cholinergic (Batchelor et al., 1989; Sobreviela et al., 1994). The goal of this study was to determine whether identified SH cholinergic neurons are excited by their own neurotransmitter via muscarinic receptors.
MATERIALS AND METHODS
Retrograde labeling of septohippocampal neurons.Young adult male Sprague Dawley albino rats (14- to 21-d-old) were anesthetized using the following cocktail: ketamine, 75 mg/kg; xylazine, 4 mg/kg, and acepromazine, 0.075 mg/kg. Retrograde labeling of septohippocampal neurons (SHNs) was performed by pressure injecting 50–100 nl of rhodamine-labeled fluorescent latex microspheres (Lumafluor, Naples, FL) at several sites within the hippocampus of 14- to 21-d-old rats using a glass micropipette (40–50 μm tip diameter). Rhodamine microspheres (0.02–0.2 μm diameter) show little diffusion and consequently produce small, sharply defined injection sites. Once transported back to neuronal somata, the label persists for at least 10 weeks in vivo and 1 year after fixation. Microspheres have been reported to possess no obvious cytotoxicity or phototoxicity, as assessed by intracellular recording and staining of retrogradely labeled cells in brain slice preparation (Katz et al., 1984). The stereotaxic coordinates were: anteroposterior, −2.8, −1.4, −2.8; lateral, −4, −1.4, −2.8; and ventral, −5.8,−4.5, −3.5 to −6 mm track). Two or more days later, the injected rats were used to prepare brain slices. Injection sites were confirmed for each experiment.
Labeling of septohippocampal cholinergic neurons using Cy3–192IgG. In anesthetized rats Cy3–192IgG (3–5 μl; 0.4 mg/ml) was stereotaxically injected unilaterally or bilaterally into the lateral ventricle of each rat with a Hamilton syringe (22 gauge needle) at a rate of 0.5 μl/min. The coordinates used were: 0.8 mm posterior from bregma, 1.2 mm lateral from midline, and 3–4 mm below the dura. Two to five days later, slices were prepared from Cy3–192IgG-injected rats and used for electrophysiological recordings. Recordings from unlabeled neurons were restricted to animals injected biventricularly.
Colocalization studies. Brain tissue taken from Cy3–192IgG-injected rats was immersion-fixed and, then, consecutive 50 μm sections of the MSDB were cut on a Vibratome. Alternate sections were immunostained for either choline acetyltransferase (ChAT) or the calcium-binding protein, parvalbumin (Parv). For the ChAT immunoreaction, the sections were incubated in a rat-anti-ChAT primary antibody (1:5 dilution in PB; Boehringer Mannheim, Indianapolis, IN) overnight at room temperature. Subsequently, sections were incubated in rabbit anti-rat IgG-fluorescein-labeled (1:100 in PB; Vector Laboratories, Burlingame, CA; FI4000) for 2 hr at room temperature in the dark. For Parv, the sections were incubated in a rabbit anti-Parv (1:500 dilution in PB; gift of K. G. Baimbridge, Vancouver, Canada; overnight at room temperature) followed by goat anti-rabbit IgG-fluorescein (1:100 in PB; Vector Laboratories; FI1000; 2 hr at room temperature in the dark).
Immunofluorescence was visualized under an Olympus BX50WI scope (Olympus Optical, Tokyo, Japan) using the appropriate filters for Cy3 and fluorescein. Cy3 appeared as granules within the cytoplasm of the cells, whereas the ChAT and Parv immunofluorescence was homogeneously distributed in the cells. This made it easy to confirm colocalization of the two substances in the same cell.
Slice preparation for electrophysiological recordings. Brain slices containing the MSDB were prepared from young adult male Sprague Dawley albino rats (2- to 4-weeks-old) using methods detailed previously (Alreja and Liu, 1996). Briefly, rats were anesthetized with chloral hydrate (400 mg/kg, i.p.) and killed by decapitation. The ACSF, pH 7.35–7.38, equilibrated with 95%O2 and 5% CO2, contained (in mm): NaCl, 126; KCl, 3; NaH2PO4, 1.25;d-glucose, 10; NaHCO3, 25; CaCl2, 2, and MgSO4, 2. After decapitation, the brain was removed and placed in a Petri dish containing ACSF and trimmed to yield a small block containing the MSDB. Coronal slices of ∼300 μm thickness containing the MSDB were cut with a vibrating-knife microtome (Frederick Haer, Bowdingham, ME) and transferred to a Plexiglas recording chamber (1.5 ml volume) on the fixed stage of an Olympus BX50WI scope. The slice was kept in place with a grid and maintained at 33 ± 0.5°C. One to two hours later the slice was used for recording. The chamber was continuously perfused with normal ACSF at a rate of 1–2 ml/min.
Fluorescence and infrared imaging. Infrared, differential interference contrast imaging (IR-DIC) (Dodt and Zieglgansberger, 1990;Stuart et al., 1993) was performed to visualize neurons for extracellular or patch-clamp recording using an Olympus Optical BX-50 microscope equipped with a 60× water immersion objective (numerical aperture, 0.9; Olympus). Images were detected with a CCD-300-RC camera (DAGE-MTI, Michigan City, IN) and displayed on a standard black and white video monitor (DAGE-MTI, HR 120). The images were transferred to the hard disk of a personal computer using an LG-3 scientific frame grabber (Scion Image, Frederick, MD) and processed further with Adobe Photoshop. Cy3–192IgG-labeled and rhodamine-labeled neurons were visualized using the appropriate fluorescence filters, as was Lucifer yellow. A neuron viewed with infrared optics was considered to be the same as that viewed with fluorescence optics when the infrared image and the fluorescent image of the neuron had the same position and orientation with the two imaging systems.
Electrophysiology recordings. The image of the cells in the slice was displayed on a video monitor, and glass pipettes used for electrophysiological recordings were visually advanced through the slice to the surface of the cell from which recordings were made. Extracellular recordings were performed with glass micropipettes filled with 2 m NaCl (5–10 MΩ). Whole-cell patch-clamp recordings were performed using previously described methods (Alreja and Liu, 1996). In brief, low-resistance (2.5–3.5 MΩ) patch pipettes were filled with a solution containing (in mm): K methylsulfonate/KCl, 120; HEPES, 10; BAPTA K4, 5; sucrose, 20; CaCl2, 2.38; MgCl2, 1; K2ATP, 1 and GTP, 0.1, pH 7.32–7.35. All recordings were made using an Axoclamp-2B amplifier (Axon Instruments, Foster City, CA) in the bridge mode; the output signal was filtered at 10 kHz. The cells selected for study had spike amplitudes of 70–100 mV. Spike durations were measured at half-spike amplitude. In spontaneously firing cells these measurements were done at the resting potential and in quiescent cells, firing was evoked by injecting a small amount of depolarizing current. Voltage-clamp recordings were performed using the continuous single-electrode voltage-clamp mode. The firing rate, current, and voltage signals were amplified and continuously recorded on a chart recorder (Gould 2200). For intracellular labeling studies, Lucifer yellow (1%) was added to the patch pipette solution.
Double-labeling studies. To determine the phenotype of cells recorded with Lucifer yellow-containing patch pipette solutions, double-labeling studies were performed on slices fixed using 4% paraformaldehyde solution. For the ChAT immunoreaction, the sections were incubated in a rat anti-ChAT primary antibody (1:5 dilution in PB; Boehringer Mannheim) overnight at room temperature. Subsequently, sections were incubated in rabbit anti-rat IgG, Texas Red-labeled (1:100 in PB; Vector Laboratories) for 2 hr at room temperature in the dark.
Materials. Acetylcholine chloride, muscarine chloride, atropine sulfate, and (−)-scopolamine hydrobromide were obtained from Research Biochemicals (Natick, MA). All drugs were diluted in ACSF from previously prepared stock solutions that were prepared in water and stored at −20°C. Rhodamine microspheres were obtained from Lumafluor (Naples, FL), and Cy3–192IgG was custom-synthesized by Advanced Targeting Systems (San Diego, CA).
RESULTS
Muscarinic agonists excite retrogradely labeled septohippocampal neurons
As mentioned above, antidromically activated SHNs have been shown to be excited by muscarinic receptor agonists both in vivo(Dutar et al., 1983; Lamour et al., 1984) and in vitro in a concentration-dependent and atropine-sensitive manner (Liu et al., 1998). The phenotype of the excited neurons, while presumed to be cholinergic, has actually never been confirmed (Lamour et al., 1984). Before initiating studies on identified septohippocampal cholinergic neurons, we used a second technique, the technique of retrograde labeling to confirm the effects of muscarine on unidentified SHNs. Extracellular recordings were performed in retrogradely marked SHNs in rat brain slices prepared from rats in which the retrograde tracer, rhodamine microspheres, was injected directly into the rat hippocampus (Fig. 1A). ACh (1 mm) and/or muscarine (1–10 μm) produced a profound excitatory effect in 8 of 13 SHNs tested (Fig. 1B), which resulted in a 31–300% increase in firing rate (mean, 138 ± 42%). These neurons had basal firing rates of 9.1 ± 2.2 Hz (range, 2–19 Hz); ACh/muscarine produced a statistically significant increase in rate (p < 0.001; mean, 16.3 ± 2.5 Hz; range, 8–25 Hz). Four of 13 SHNs tested in this study did not respond to muscarine, and one was inhibited by muscarine. All effects of ACh–muscarine were blocked by the muscarinic receptor antagonist atropine (100 nm to 3 μm). As expected, both the lower and the higher concentrations of the antagonists blocked the ACh–muscarine responses; the higher concentrations however, had a much more rapid effect. These observations thus confirm earlier studies that have reported the presence of muscarine-excited MSDB neurons that project to the hippocampus.
Cy3–192IgG selectively labels septohippocampal cholinergic neurons in the MSDB
To test the effect of muscarine on identified septohippocampal cholinergic neurons, we injected rats, intraventricularly, with the novel fluorescent marker, Cy3–192IgG. Cy3–192IgG selectively labels septohippocampal cholinergic neurons in the MSDB (Hartig et al., 1998).
Before initiating electrophysiological recordings, we performed double-labeling studies to confirm the selectivity of Cy3–192IgG as a marker for cholinergic neurons in the MSDB. Two to five days after unilateral or bilateral intraventricular injections of Cy3–192IgG, retrogradely labeled, red-fluorescent neurons could be observed in the MSDB. Consistent with published findings, Cy3–192IgG-labeled MSDB neurons were found to colocalize the enzyme ChAT, a well established marker of cholinergic neurons (Fig.2A); all cholinergic neurons however did not get labeled with Cy3–192IgG, presumably because of incomplete diffusion of Cy3–192IgG (Hartig et al., 1998). In addition, we performed double-labeling studies using an antibody against the calcium-binding protein parvalbumin. In the MSDB, parvalbumin is selectively contained in septohippocampal GABA neurons (Freund, 1989). We found that parvalbumin-positive neurons never colocalized Cy3–192IgG (Fig. 2B). As expected, Cy3–192IgG -labeled neurons also did not colocalize the enzyme glutamic acid decarboxylase (GAD); which is expressed both by local as well as by projection GABAergic neurons (data not shown). Thus, the selectivity of Cy3–192IgG for cholinergic neurons is similar to that reported for the well-established immunotoxin 192IgG–saporin (Wenk et al., 1994; Wiley et al., 1995).
Therefore, although the Cy3–192IgG-labeled neuronal population in the MSDB is exclusively cholinergic, the unlabeled population although primarily GABAergic (local and projection), also includes unlabeled cholinergic neurons. With these findings in view, we tested the effects of muscarinic agonists on both Cy3–192IgG-labeled and unlabeled neurons.
Muscarine does not excite Cy3–192IgG-labeled MSDB neurons but profoundly excites unlabeled MSDB neurons
Extracellular and whole-cell recordings were made from Cy3–192IgG-labeled and unlabeled MSDB neurons visualized in rat brain slices using an IR-DIC videomicroscope equipped with appropriate filters for visualization of fluorescence. Cy3–192IgG-labeled neurons appeared as red fluorescent neurons with a punctate-type staining (Fig.3), presumably because of clustering of the red fluorescent antibodies in compartments resembling lysosomes (Hartig et al., 1998). Cy3–192IgG-labeled neurons had a healthy appearance (Fig. 3); 43% of the neurons from which we recorded (n = 53) fired spontaneously at a rate of 2 ± 0.07 Hz recorded extracellularly. Whole-cell recordings were also established in 37 of 53 neurons tested. These neurons exhibited electrophysiological characteristics similar to those described for cholinergic neurons using double-labeling techniques by previous workers (see below).
The effect of ACh and/or the muscarinic receptor agonist, muscarine (1–10 μm) was tested in a total of 47 Cy3-labeled neurons. Surprisingly, none of the Cy3–192IgG-labeled neurons tested were excited by ACh–muscarine, although they were strongly excited by the excitatory amino acid glutamate (n = 18; data not shown). Instead, muscarine produced inhibitory responses (Fig.4A) in 62% (29 of 47) of the Cy3-labeled neurons (1–10 mV hyperpolarization; mean, 3.5 ± 0.6 mV). The remaining 38% neurons were not affected by muscarine.
In sharp contrast to the effects of ACh–muscarine on Cy3–192IgG-labeled neurons, 91% of the unlabeled neurons (31 of 34) were profoundly excited by ACh–muscarine (Fig. 4B) and showed a 19–600% increase in firing rate (mean, 192 ± 36%). These neurons had basal firing rates of 4.2 ± 0.5 Hz (range, 0.6–11.5 Hz); ACh–muscarine produced a statistically significant increase in rate (p < 0.001; mean, 11.3 ± 0.9 Hz; range, 1.7–25 Hz). Two neurons were not affected by ACh–muscarine, whereas one neuron was inhibited. These data are summarized in Figure 4, C and D. Consistent with previous observations, repeated applications of ACh–muscarine had a similar effect and did not show any desensitization (Liu et al., 1998).
All effects of ACh–muscarine, both excitatory and inhibitory, in labeled and unlabeled neurons, were blocked by the muscarinic receptor antagonists, atropine, or scopolamine (100 nm to 3 μm; n = 8).
Thus, the sampled Cy3–192IgG neuronal population discussed above, which is exclusively cholinergic, was found never to be excited by muscarine. This raises an important issue: if the septohippocampal neurons that are excited by muscarine are not cholinergic, then what is their phenotype? As mentioned before, a subpopulation of GABA neurons in the MSDB also projects to the hippocampus via the fimbria-fornix.
Muscarine-excited MSDB neurons are noncholinergic, septohippocampal GABA-type
The GABA neurons that project to the hippocampus from the MSDB are distinct from other neurons in the MSDB (cholinergic and local GABA) in that they exclusively express the calcium-binding protein parvalbumin (Freund, 1989). Because of this unique property, parvalbumin has become a well established marker of septohippocampal GABA neurons in the MSDB (Gao et al., 1995; Leranth and Vertes, 1999). Parvalbumin-containing neurons in the cortex (Kawaguchi and Kubota, 1997), hippocampus (Sik et al., 1995), and more recently in the MSDB (Morris et al., 1999), have been shown to possess unique spiking properties, such as a lack of spike frequency accommodation and thus an ability to fire rapidly; properties that may be reflective of the calcium-buffering properties of parvalbumin. Additionally, in the MSDB, parvalbumin-positive neurons have been reported to be spontaneously firing, possess short duration spikes (0.3–0.7 msec), and exhibit a depolarizing sag in response to a hyperpolarizing current.
To determine if muscarinic agonists excite MSDB neurons possessing electrophysiological characteristics of parvalbumin-positive neurons (and therefore of septohippocampal GABA-type neurons), we performed whole-cell recordings in brain slices taken from noninjected rats and noted the effect of muscarinic agonists on MSDB neurons that clearly exhibited the abovementioned electrophysiological criteria of parvalbumin-positive neurons. Of the 16 MSDB neurons so characterized, 14 were found to respond to muscarinic agonists with a profound excitation (Fig. 5A). These neurons had basal firing rates of 5.6 ± 1 Hz (range, 1–18 Hz), which increased to 17–25 Hz after application of muscarine (p < 0.001; n = 5). One neuron was inhibited by muscarine. In eight neurons, the effect of muscarine was tested under voltage clamp at a holding potential of −60 mV, muscarine produced a 50–80 pA inward current in the eight neurons tested (mean, 52.5 ± 0.7 pA; data not shown). Thus, similar to unlabeled neurons above, muscarinic agonists were found to excite a vast majority of parvalbumin-type MSDB neurons (87.5%).
Again, in contrast, to the parvalbumin-containing, septohippocampal GABA-type neurons, neurons exhibiting electrophysiological properties of cholinergic-type neurons (also recorded from slices taken from noninjected rats), were found never to be excited by muscarine. Cholinergic-type neurons in uninjected rats therefore responded to muscarine in a manner similar to the Cy3–192IgG-labeled population described above. Whereas 10 of 16 (62.5%) cholinergic-type neurons were inhibited by muscarine (1–10 mV hyperpolarization), the remaining six neurons were not affected by muscarine (Fig. 5B). Sixty percent of the neurons were spontaneously firing (range, 0.1–2 Hz; mean, 1.2 ± 0.2 Hz). The electrophysiological criteria used for identification of cholinergic-type MSDB neurons included the presence of a prolonged spontaneous afterhyperpolarization (200–700 msec) after a single spike and presence of anomalous rectification but no depolarizing sag in response to hyperpolarizing pulses; these criteria were based on those described by earlier workers (Griffith and Matthews, 1986; Markram and Segal, 1990; Gorelova and Reiner, 1996). The data on cholinergic-type and parvalbumin-type neurons is summarized in Figure 5, C and D.
The effect of the muscarinic agonist was also tested in presence of tetrodotoxin (TTX). Whereas the excitatory response to muscarine persisted in presence of TTX in all six neurons tested, the inhibitory response in cholinergic-type neurons was blocked by TTX in two of five neurons tested (data not shown). In both these neurons the TTX-sensitive muscarinic inhibition was accompanied by an increase in the frequency of inhibitory synaptic activity, which is both TTX- and bicuculline-sensitive (Kumar et al., 1997). Thus, cholinergic-type neurons in the MSDB exhibited both direct postsynaptic as well as indirect inhibitory responses.
To further confirm the noncholinergic phenotype of the neurons excited by muscarine, we labeled MSDB neurons with Lucifer yellow during whole-cell recordings and, after completion of the experiment, we performed double-labeling studies using an antibody against the enzyme ChAT, which is a well established marker of cholinergic neurons. Of the eight successfully double-labeled neurons, five were excited by muscarine, and the remaining three were not affected. Interestingly, the five neurons that were excited by muscarine were all found to be ChAT-immunonegative, supporting the above findings that suggested that the neurons excited by muscarine are noncholinergic. All the ChAT-immunonegative neurons had electrophysiological properties similar to those that have been described for septohippocampal GABA neurons (see above). Of the three neurons that were not affected by muscarine, one colocalized ChAT, and two were ChAT-immunonegative.
In conclusion, septohippocampal cholinergic neurons were never found to be excited by muscarine, whereas noncholinergic, septohippocampal GABA-type neurons were profoundly excited by muscarine.
DISCUSSION
The main findings of this study are: (1) muscarinic receptor agonists do not excite septohippocampal cholinergic neurons, and (2) noncholinergic, septohippocampal GABA-type MSDB neurons are strongly excited by muscarinic agonists. These findings, therefore, challenge the current belief that MSDB cholinergic neurons are excited by their own neurotransmitter and that this excitation and the subsequent increase in hippocampal ACh underlies the improvement in learning and memory that is observed after intraseptal administration of muscarinic drugs.
Muscarinic agonists do not excite septohippocampal cholinergic neurons
Using a fluorescent labeling technique, involving the p75-receptor antibody conjugated to the Cy3 fluorochrome for selective visualization of septohippocampal cholinergic neurons located in the MSDB, we have found no excitatory effects of muscarine on Cy3–192IgG-labeled septohippocampal cholinergic neurons. In fact, Cy3-labeled septohippocampal cholinergic neurons are either inhibited or not affected by muscarine. Recordings from cholinergic-type MSDB neurons (in brain slices prepared from noninjected rats), classified according to previously published electrophysiological criteria, also yielded the same results. Therefore, the presence of Cy3–192IgG in septohippocampal cholinergic neurons does not appear to alter their responsivity to muscarinic agonists. The electrophysiological properties of Cy3-labeled neurons were also similar to those of cholinergic-type neurons recorded from noninjected rats, suggesting that Cy3–192IgG may be a useful tool worthy of being exploited for future studies on septohippocampal cholinergic neurons as well as on p75 receptor-expressing neurons elsewhere in the brain, such as in the nucleus basalis.
The finding that septohippocampal cholinergic neurons are not excited by muscarine is very interesting because intaseptal injections of muscarinic agonists elicit continuous hippocampal theta rhythm and produce behavioral improvements in working and memory tasks both in young and aged rats (see introductory remarks). Our results indicate that the mechanisms underlying intraseptal muscarinic agonist-induced improvements in learning and memory and production of theta rhythm do not involve an impulse-dependent increase in hippocampal ACh release. This conclusion is supported by the findings of microdialysis studies that show that infusions of muscarinic agonists into the MSDB produce a dose-dependent decrease in hippocampal ACh release (Gorman et al., 1994) or have no effect (Moor et al., 1995). A decrease in hippocampal ACh release would be predicted by the results of the present study because 60–65% of septohippocampal cholinergic neurons from which we recorded were found to be inhibited by muscarine.
The finding that a subpopulation of septohippocampal cholinergic neurons is inhibited by muscarine is consistent with light-microscopic colocalization studies that have demonstrated the presence of m2 receptor immunoreactivity (a muscarinic receptor associated with inhibitory responses) in a subset of choline acetyltransferase-immunoreactive as well as noncholinergic neurons (Van der Zee and Luiten, 1994; Levey et al., 1995) and retrogradely labeled septohippocampal neurons (Rouse and Levey, 1996). m2 receptor mRNA has also been shown to colocalize with cholinergic MSDB neurons (Vilaro et al., 1992).
Muscarinic agonists excite noncholinergic, septohippocampal GABA-type neurons
The finding that muscarinic agonists do not have any excitatory effects on septohippocampal cholinergic neurons raises the question of what cellular mechanism or mechanisms might mediate the effects of intraseptal muscarinic drugs on learning and memory and the associated theta rhythm. The results of the present study as well as previously published studies clearly show that muscarine-excited MSDB cells do project to the hippocampus (Dutar et al., 1983; Lamour et al., 1984;Liu et al., 1998), suggesting then that the muscarine-excited neurons must then be GABAergic. As mentioned previously, similar to the cholinergic neurons, the septohippocampal GABA neurons also project to the hippocampus via the fimbria-fornix. In fact, in our earlier study using the technique of antidromic activation, we found that septohippocampal neurons excited by muscarine had fast-conducting fibers, with conduction velocities greater than 1 m/sec, which may be suggestive of GABA neurons (Liu et al., 1998).
In the present study, muscarinic agonists consistently produced a strong excitation of unlabeled neurons in Cy3–192IgG-injected rats, some of which were confirmed to be noncholinergic using the technique of double labeling. Because Cy3–192IgG does not label parvalbumin-positive or GAD-positive neurons of the MSDB, it is likely that the unlabeled cell population, which was profoundly excited by muscarine, included the septohippocampal GABA neurons of the MSDB. Additionally, in uninjected rats a vast majority of neurons exhibiting electrophysiological properties characteristic of septohippocampal GABA-type neurons were profoundly excited by muscarine.
Implications of the findings
The present study suggests that an activation of septohippocampal GABA neurons and not septohippocampal cholinergic neurons may underlie the behavioral and electrophysiological effects observed after intraseptal infusions of muscarinic agonists in rats. Whereas most published research has focused on the importance of septohippocampal cholinergic mechanisms in learning and memory functions and in generation of the theta rhythm, the role of septohippocampal GABAergic mechanisms is being increasingly recognized, especially with regard to production of theta activity (Stewart and Fox, 1990; Bassant et al., 1995; Brazhnik and Fox, 1997, 1999; Monmaur et al., 1997). The results of the present study suggest that the reported effects of intraseptal carbachol on theta rhythm (Monmaur and Breton, 1991; Lawson and Bland, 1993) cannot be attributed to an increase in firing of septohippocampal cholinergic neurons. Therefore, the question is, how important are the cholinergic neurons for carbachol-induced generation of theta rhythm? Buzsaki's laboratory has demonstrated that intraseptal infusions of carbachol continue to elicit theta activity in the hippocampus even in the complete absence of MSDB cholinergic neurons in 192IgG–saporin-treated rats, albeit, at a reduced amplitude, thereby indicating a critical role of septohippocampal GABAergic neurons in generation of theta rhythm (Lee et al., 1994).
Anatomically, the septohippocampal GABA neurons are well positioned to exert indirect but strong effects on hippocampal pyramidal neurons. In contrast to the septohippocampal cholinergic neurons, which innervate almost every type of neuron in the hippocampus (pyramidal cells, dentate granule cells, inhibitory interneurons) (Frotscher and Leranth, 1985), the septohippocampal GABA neurons selectively innervate only the GABA interneurons of the hippocampus (Freund and Antal, 1988). Via this very selective connectivity, the septohippocampal GABA neurons can theoretically produce a powerful disinhibitory effect on hippocampal pyramidal neurons. In fact, a recent study performed using a novel combined septohippocampal slice preparation has provided electrophysiological evidence that activation of septohippocampal GABAergic fibers can lead to a disinhibition of pyramidal cells (Toth et al., 1997). Therefore, it is conceivable that a profound muscarinic agonist-induced excitation of septohippocampal GABA neurons, as was observed in the present study, could, via hippocampal interneurons, produce a powerful disinhibition of pyramidal cells and possibly promote induction of long-term potentiation in the hippocampus. Long-term potentiation is preferentially induced when the pyramidal cells are maximally stimulated (Pavlides et al., 1988).
In addition to muscarinic agonists, serotonin, primarily via 5-HT2A receptors, (Alreja, 1996; Liu et al., 1997), and norepinephrine, via α1 receptors (Alreja and Liu, 1996), also excite septohippocampal GABA neurons, albeit, not as profoundly as muscarine. Opioids, on the other hand, via mu receptors, inhibit septohippocampal GABA neurons (Alreja et al., 2000). Interestingly, behavioral studies have reported that intraseptal infusions of opioids (Bostock et al., 1988; Ragozzino et al., 1992) or α1 noradrenergic receptor antagonists (Marighetto et al., 1989), treatments that would decrease impulse flow in the septohippocampal GABA pathway, impair learning and memory.
Pharmacologically, the excitatory effects of muscarinic agonists on septohippocampal neurons are mediated via non-M1type muscarinic receptors (M3 and possibly M5 subtypes) (Liu et al., 1998). Thus, muscarinic agonists directed toward the M3 and M5 receptor subtypes, could, theoretically by mimicking the behavioral effects of muscarine, alleviate age-related amnesia as age-related amnesia, and decrease in theta power can be alleviated by intraseptal infusions of muscarinic agonists in rats (Markowska et al., 1995). If mechanisms similar to those that occur in aged rats also contribute to dementias associated with Alzheimer's, Parkinsonism, or even those associated with mental illnesses such as schizophrenia, then M3 and M5-receptor agonists could prove useful therapeutically.
Footnotes
This work was supported by National Alliance for Research on Schizophrenia and Depression and National Institutes of Health Grants DA09797 to M.A. and NS26068 to C.L. We thank N. Margiotta for technical help and Leslie Rosello for help in manuscript preparation.
Correspondence should be addressed to Dr. Meenakshi Alreja, Department of Psychiatry, CMHC 335A, Yale University School of Medicine, 34 Park Street, New Haven, CT 06508. E-mail: Meenakshi.Alreja{at}yale.edu.