SPINOTHALAMIC AND SPINOHYPOTHALAMIC TRACT NEURONS IN THE SACRAL SPINAL-CORD OF RATS .1. LOCATIONS OF ANTIDROMICALLY IDENTIFIED AXONS IN THECERVICAL CORD AND DIENCEPHALON
Jt. Katter et al., SPINOTHALAMIC AND SPINOHYPOTHALAMIC TRACT NEURONS IN THE SACRAL SPINAL-CORD OF RATS .1. LOCATIONS OF ANTIDROMICALLY IDENTIFIED AXONS IN THECERVICAL CORD AND DIENCEPHALON, Journal of neurophysiology, 75(6), 1996, pp. 2581-2605
1. A goal of this study was to determine the sites in the diencephalon
to which neurons in sacral spinal segments of rats project. Therefore
, 95 neurons were recorded extracellularly in spinal segments L(6)-S-2
Of rats that were anesthetized with urethan. These neurons were activ
ated initially antidromically with currents less than or equal to 30 m
u A from a monopolar stimulating electrode placed into the contralater
al posterior diencephalon. The mean +/- SE current for antidromic acti
vation from these sites was 16 +/- 0.8 mu A. These neurons were record
ed in the superficial dorsal horn (4%), deep dorsal horn (89%), and in
termediate zone and ventral horn (4%). 2. Systematic antidromic mappin
g techniques were used to map the axonal projections of 41 of these ne
urons within the diencephalon. Thirty-three neurons (80%) could be act
ivated antidromically with currents less than or equal to 30 mu A only
from points in the contralateral thalamus and are referred to as spin
othalamic tract (STT) neurons. Eight neurons (20%) were activated anti
dromically with low currents from points in both the contralateral tha
lamus and hypothalamus, and these neurons are referred to as spinothal
amic tract/spinohypothalamic tract (STT/SHT) neurons. Three additional
neurons were activated antidromically with currents less than or equa
l to 30 mu A only from points within the contralateral hypothalamus an
d are referred to as spinohypothalamic tract (SHT) neurons. The dience
phalic projections of another 51 neurons were mapped incompletely. The
se neurons are referred to as spinothalamic/unknown (STT/U) neurons to
indicate that it was not known whether their axons ascended beyond th
e site in the thalamus from which they initially were activated antidr
omically. 3. For 31 STT neurons, the most anterior point at which anti
dromic activation was achieved with currents less than or equal to 30
mu A was determined. Fourteen (45%) were activated antidromically only
from sites posterior to the ventrobasal complex (VbC) of the thalamus
. Sixteen STT neurons (52%) were activated antidromically with low cur
rents from sites at the level of the VbC, but not from more anterior l
evels. One STT neuron (3%) was activated antidromically from the anter
oventral nucleus of the thalamus. 4. STT/SHT neurons were antidromical
ly activated with currents less than or equal to 30 mu A from the medi
al lemniscus (ML), anterior pretectal nucleus (Apt), posterior nuclear
group and medial geniculate nucleus (Po/MG), and zona incerta in the
thalamus and from the optic tract (OT), supraoptic decussation, or lat
eral area of the hypothalamus. No differences in the sites in the thal
amus from which STT and STT/SHT neurons were activated antidromically
were apparent. Five STT/SHT neurons (62%) were activated antidromicall
y from points in the thalamus in the posterior diencephalon and from p
oints in the hypothalamus at more anterior levels. Three STT/SHT neuro
ns (38%) were activated antidromically with currents less than or equa
l to 30 mu A from sites in both the thalamus and hypothalamus at the s
ame anterior-posterior level of the diencephalon. All three of these S
TT/SHT neurons projected to the intralaminar nuclei (parafascicular or
central lateral nuclei) of the thalamus. 5. Seven STT/SHT neurons wer
e tested for additional projections to the ipsilateral brain. Two (29%
) were activated antidromically with currents less than or equal to 30
mu A and at longer latencies from sites in the ipsilateral diencephal
on. One could only be activated antidromically from the hypothalamus i
psilaterally. The other was activated antidromically at progressively
increasing latencies from points in the ipsilateral brain that extende
d as far posteriorly as the posterior pole of the MG. 6. Fifty-eight S
TT, STT/SHT, and STT/U neurons were classified as low-threshold (LT),
wide dynamic range (WDR), or high-threshold (HT) neurons based on thei
r responsiveness to innocuous and noxious mechanical stimuli applied t
o their cutaneous receptive fields. There were no statistically signif
icant differences among the numbers of LT, WDR, and HT neurons categor
ized as STT or STT/SHT neurons. For STT neurons, the most anterior poi
nts from which LT neurons were activated antidromically with low curre
nts were located in and adjacent to the VbC. In contrast, the most ant
erior points from which nociceptive (WDR and HT) neurons were activate
d antidromically tended to be located posterior to the VbC in the ML,
Apt, OT, and Po/MG. This difference in the apparent termination patter
ns of LT and nociceptive (WDR and HT) STT neurons was statistically si
gnificant. 7. STT and STT/SHT neurons also were tested for their respo
nsiveness to either colorectal (CrD) or vaginal (VaD) distention, or t
o both. Nine of 23 STT neurons (39%) and three of four STT/SHT neurons
(75%) were excited by CrD. Five of 14 STT neurons (36%) and two of fo
ur STT/SHT neurons (50%) were excited by VaD. Four STT and two STT/SHT
neurons were excited by both CrD and VaD and two STT neurons were exc
ited by CrD but not VaD. There were no statistically significant diffe
rences among the numbers of STT and STT/SHT neurons that were excited
by either CrD or VaD. 8. Using a second stimulating electrode, 80 STT,
STT/SHT, and STT/U neurons also were activated antidromically with cu
rrents less than or equal to 30 mu A from the contralateral white matt
er of upper cervical segments. More than 90% of these neurons were act
ivated from the lateral half of the contralateral lateral funiculus. T
wenty-two of these neurons were activated antidromically from both C-4
and C-2. At all cervical levels, the majority was activated antidromi
cally from the ventrolateral funiculus (VLF). No segregation of axons
in the dorsolateral funiculus or VLF according to diencephalic project
ions, recording site, or physiological classification was apparent. 9.
Conduction velocities from the recording point to sites in C-4, C-2,
and the brain from which STT, STT/SHT, and STT/U neurons were activate
d antidromically were calculated. The mean +/- SE conduction velocity
to C-4 was 22.5 +/- 1.0 m/s, to C-2 was 21.5 +/- 1.9 m/s, and to the i
nitial low-threshold point in the brain was 19.8 +/- 0.9 m/s. The mean
conduction velocity to the brain was significantly slower than those
to C-4 and C-2. The mean conduction velocities to C-4 and C-2 were nut
significantly different. IO. Our findings demonstrate that neurons in
spinal segments L(6)-S-2 Of rats issue axons that ascend co