A b s t r a c t T h e n i n e -b a n d e d a r m a d i l l o , D a s y p u s novemcinctus, is a member of the family Dasypodidae, which contains all extant species of armadillos and represents the most diverse group of xenarthran mammals by their speciation, form, and range of scratch-digging ability. This study aims to identify muscle traits that reflect specialization for fossorial habit by observing forelimb structure in D. novemcinctus and comparing it among armadillos using available myological data. A number of informative traits were observed in D. novemcinctus and among Dasypodidae, including the absence of m. rhomboideus profundus, the variable presence of a m. articularis humeri and m. coracobrachialis, two heads of m. triceps brachii with scapular origin, and a lack of muscle mass devoted to antebrachial supination. Muscle mass and myosin heavy chain (MHC) isoform content were also quantified from our forelimb dissections. New osteological indices are additionally calculated and reported for D. novemcinctus. Collectively, the findings emphasize muscle mass and power output for limb retraction and specialization of the distal limb for sustained purchase of soil by strong pronation and carpal/digital flexion. Moreover, the myological traits assessed here provide a valuable resource for interpretation of muscle architecture specializations among digging mammals and future reassessment of armadillo phylogeny.

SUMMARY1. Voltage-clamp recordings using a single microelectrode were obtained from pyramidal neurones of the basolateral amygdala (BLA) in slices of the rat ventral forebrain. Slow inward current relaxations during hyperpolarizing voltage steps from a holding potential of -40 mV were identified as the muscarinic-sensitive Mcurrent (1M), a time-and voltage-dependent potassium current previously identified in other neuronal cell types.2. Activation of IM was voltage dependent with a threshold of approximately -70 mV. At membrane potentials positive to this, the steady-state current-voltage (I-V) relationship showed substantial outward rectification, reflecting the time-and voltage-dependent opening of M-channels. The underlying conductance (gm) also increased sharply with depolarization.3. The reversal potential for IM was -84 mV in medium containing 3-5 mm K+. This was shifted positively by 27 mV when the external K+ concentration was raised to 15 mM.4. The time courses of M-current activation and deactivation were fitted by a single exponential. The time constant for IM decay, measured at 24 'C, was strongly dependent on membrane potential, ranging from 330 ms at -40 mV to 12 ms at -100 mV. of -70 mV so that it crossed the control I-V plot at the reversal potential for 'Leak. This was found to be -108 mV in 3-5 mm KI saline, shifting to -66 mV in 15 mm K+ saline. However, in a few neurones, carbachol produced a parallel shift of the instantaneous I-V relationship and no reversal potential could be obtained, possibly due to the activation by carbachol of a non-specific cation conductance.8. In unclamped BLA pyramidal neurones, carbachol produces a slow membrane depolarization accompanied by an increase in input resistance. It is concluded that these actions are mediated by muscarinic receptor activation, resulting in inhibition of both the M-current and a voltage-independent K+ leak current.

The excitability level of pyramidal neurons in the basolateral amygdala (BLA) is greatly increased following muscarinic receptor activation, an effect associated with an increased rate of action potential firing and reduction of the afterhyperpolarization (AHP). We impaled BLA pyramidal neurons in slices of rat ventral forebrain with a single microelectrode to examine the currents underlying the AHP and spike frequency accommodation and determine their sensitivities to muscarinic modulation. In voltage-clamp, depolarizing steps were followed by biphasic outward tail currents, consisting of rapidly decaying (IFast) and slowly decaying (ISlow) current components. These corresponded temporally with the medium and slow portions of the AHP, respectively. The reversal potential for the IFast component of the AHP tail current shifted in the depolarizing direction with increases in the extracellular K+ concentration. The amplitude of IFast was reduced during perfusion of 0-Ca2+ medium or by superfusion of TEA (1-5 mM) or carbachol (10-40 microM). It is suggested that IFast was produced by the rapidly decaying Ca(2+)-activated K+ current (IC) and the muscarinic-sensitive M-current (IM). The ISlow tail current component reversed at the estimated values for EK in medium containing either normal or elevated K+ levels. This component was eliminated by perfusion of 0-Ca2+ medium or inclusion of cyclic-AMP in the recording electrode. It was not blocked by TEA (5 mM) or apamin (50-500 nM), but was reduced by carbachol in a dose-dependent manner (IC50 = 0.5 microM). Electrical stimulation of cholinergic afferent pathways to the BLA produced inhibition of ISlow, an effect which was enhanced by eserine and prevented by atropine. Loss of the ISlow component was always accompanied by similar reductions in accommodation and the slow AHP. It was concluded that this tail current component resulted from the slowly decaying Ca(2+)-activated K+ current, IAHP. Thus, the muscarinic inhibition of IAHP contributes to the enhanced excitability exhibited by BLA pyramidal neurons following cholinergic stimulation.

1. A single microelectrode was used to obtain current-clamp or voltage-clamp recordings from two neuronal cell types (pyramidal and late-firing neurons) in the basolateral nucleus of the amygdala (BLA) in slices of the rat ventral forebrain. Conductances activated by hyperpolarizing voltage steps from a holding potential of -70 mV were identified and their sensitivity to muscarinic modulation was determined using bath superfusion of carbachol. 2. Unclamped pyramidal neurons exhibited anomalous rectification, seen as a slowly developing depolarizing sag in the electronic potential in response to a hyperpolarizing current pulse. 3. Stepping voltage-clamped pyramidal neurons to command potentials of between -70 and -100 mV activated a slowly developing inward current (ISlow) that followed a single exponential time course. Larger hyperpolarizing voltage steps evoked a rapidly developing inward current (IFast) that preceded the development of ISlow. 4. The ISlow component reversed at a level positive to the -70 mV holding potential. Its rate of activation accelerated as the hyperpolarizing voltage step was made more negative. The threshold for activation of the conductance underlying ISlow was approximately -60 mV, with half-activation occurring at -90 mV. 5. Extracellular Cs+ (2 mM) blocked ISlow and eliminated anomalous rectification in unclamped pyramidal neurons. The inhibition of ISlow by Cs+ was also associated with membrane hyperpolarization and reduction of the medium afterhyperpolarization. ISlow was unaffected by extracellular Ba2+ (100 microM). The properties of this current appeared similar to that of the mixed cationic H-current previously identified in other neurons. 6. In comparison with pyramidal cells, unclamped late-firing neurons displayed a lesser but more rapidly developing anomalous rectification in response to large hyperpolarizations from rest. In voltage clamp, hyperpolarizing steps to command potentials more negative than -100 mV elicited IFast. Late-firing neurons expressed little or no ISlow. 7. The properties of IFast were identical in both pyramidal and late-firing neurons. This current reversed at a potential negative to -70 mV. Its rate of current activation increased with the magnitude of the hyperpolarizing voltage step. This rate was approximately sevenfold faster than ISlow activation recorded at the same membrane potential. IFast was blocked by 2 mM extracellular Cs+ and reduced by 100 microM extracellular Ba2+. The threshold for activation of the underlying conductance was approximately -85 mV, with half-activation occurring at -112 mV. The properties of IFast were similar to those of the inward rectifier current previously identified in other central neurons. 8. Carbachol (40 microM) largely blocked IFast without affecting its rate of activation.(ABSTRACT TRUNCATED AT 400 WORDS)

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