We observed that the levels of two key apoptotic factors, namely Bax/Bcl-2 and caspase-3, significantly increased in disc herniation surgery, but dexmedetomidine, as an anxiolytic, sedative, and analgesic medication did not have any significant effect on CSF apoptotic factors’ levels in our study.
This investigation evaluated the intrathecal dexmedetomidine effect on apoptotic factors in the CSF. Jiang et al. in an observational study on patients with traumatic brain injury (TBI), measured apoptotic factors (caspase-3, sFas, caspase-9, and cytochrome c) in the CSF. They observed that these factors were significantly increased in patients who suffered from TBI (
10). Mao et al., in different anesthesia in discectomy, observed that combined spinal-epidural anesthesia and epidural anesthesia caused no significant differences in immune function or inflammatory indices in patients with LDH (MAO) (
11). In some other studies, there was a correlation between caspases 1, 3, 6, 7, 8, 9, and 12 and TBI (
12,
13). In addition, in some studies on other apoptotic factors and TBI, there was a significant enhancement in CSF apoptotic factors (
14,
15). Korshunova et al. observed that Bcl-2 could regulate apoptotic factors in myocardial ischemia/reperfusion injury (
16). However, these studies were different from our study in terms of protocols. The increased levels of caspase-3 and Bax/Bcl-2 in the CSF of patients shortly after surgery led us to speculate that the surgical intervention may be the sole reason for this increase.
In some studies, the levels of apoptotic factors in brain tissue were measured in patients with cerebral stroke. These studies showed the pathway activation of caspases 1, 3, 8, 9, and 11, following cerebral ischemia (
17); however, Askalan et al. suggested that cell death in infarcts following brain ischemia is partially caspase-3-independent and may also be attributed to nitric oxide (
18). Alessandri et al. mentioned that caspase-dependent pathways may also occur in an acute subdural hematoma (
19). Also, in a study by Montaner et al., they observed that the serum levels of the d-dimer and caspase-3 combination might be a biochemical marker for faster stroke diagnosis (
20). Moreover, in prognosis evaluation, a study by Wang et al. mentioned that CSF caspase-3 enhancement at admission and three days after admission in aneurysmal SAH patients resulted in an unfavorable outcome. In addition, they observed that the levels of these factors were highly associated with injury severity and patients’ prognosis after SAH (
21). On the same subject, Lorente et al. have recently reported that enhanced serum levels of caspase-3 are associated with increased mortality in severe TBI cases (
22). Accordingly, most studies in this field have indicated that these factors could be prognostic in patients with different neurologic disorders.
5.1. Conclusion
We observed that dexmedetomidine as an anxiolytic, sedative, and analgesic medication in anesthesiology, if injected intrathecally, can reduce the NRS in patients undergoing lumbar open discectomy without any significant hemodynamic changes or other side effects, such as excessive sedation. This finding further confirms the earlier investigation results on this subject. Therefore, we recommend intrathecal dexmedetomidine injection for patients undergoing open discectomy as an adjunctive medication for postoperative pain control. Nevertheless, this medication did not significantly affect the CSF levels of apoptotic factors after discectomy. Finally, we believe that assessing the CSF levels of caspase-3 and Bax/Bcl-2 in a more extended postoperative period (i.e., eight, 24, and 48 hours) deserves further investigation.