Lamina I spinothalamic tract (STT) neurons are an integral component o
f the central representation of pain and temperature and thus their se
nsitivity to various analgesics needs to be examined. In the present s
tudy, the effects of successive, cumulative doses (0.125-2.0 mg/kg) of
intravenous morphine sulfate on the quantitative stimulus-response pr
operties of nociceptive lamina I STT eels have been tested in the inta
ct, barbiturate-anesthetized cat. Both nociceptive-specific (n = 7) an
d multireceptive (heat, pinch and cold sensitive; n = 7) lamina I STT
cells were inhibited in a dose-dependent manner. Parallel dose-depende
nt effects on responses to noxious heat and pinch were generally obser
ved that reduced ongoing discharge levels and the slopes of the stimul
us-response functions. However, non-STT lamina I cells (n = 5) differe
d significantly; the responses of one multireceptive (heat, pinch and
cold-sensitive) cell and the responses to pinch of 3 of 4 wide dynamic
range cells were not inhibited. In addition, two-thirds of the nocice
ptive lamina I STT cells showed enhanced responses at the lowest dose
of morphine (0.125 mg/kg). These results contrast with the varied effe
cts of morphine reported for superficial dorsal horn cells with unchar
acterized projections and they support the role of lamina I STT cells
in pain. Furthermore, these observations are consistent with previous
findings indicating that lamina I STT neurons are a distinct subpopula
tion of lamina I cells. These results support previous evidence that o
piatergic modulation of sensory activity in lamina I is functionally o
rganized.