Yue SUN, Jie ZHANG, Bindan ZHANG, et al. Improved effect and mechanism of propofol on vascular hyporeactivity in septic rats[J]. Journal of Army Medical University, 2024, 46(3): 232-239.
DOI:
Yue SUN, Jie ZHANG, Bindan ZHANG, et al. Improved effect and mechanism of propofol on vascular hyporeactivity in septic rats[J]. Journal of Army Medical University, 2024, 46(3): 232-239. DOI: 10.16016/j.2097-0927.202304053.
Improved effect and mechanism of propofol on vascular hyporeactivity in septic rats
To observe the improved effect of propofol on vascular hyporeactivity in septic rats and its underlying mechanism.
Methods
2
A total of 96 SD rats (12 weeks old
both genders
weighing 200~220 g) were randomly divided into sham group (
n
=16)
sepsis group (
n
=16
cecal ligation and puncture)
propofol group (
n
=16)
propofol+ROCK inhibitor Y-27632 group (
n
=16)
propofol+PKCα inhibito
r GO6976 group (
n
=16)
propofol+IP3 inhibitor 2-APB group (
n
=8) and propofol+gap junction inhibitor metoclopramide sodium (Movens) group (
n
=8).
In vitro
vascular ring reactivity and vascular calcium sensitivity were measured to observe the improved effects of propofol on vascular hyporeactivity in septic rats and its relationships with RhoA/ROCK
PKCα
IP3 and cell gap junction.
Results
2
Determination of
in vitro
vascular ring and calcium sensitivity showed that the contractile reactivity to norepinephrine (NE) and to calcium sensitivity were significantly decreased in the arterial rings isolated from the septic rats compared with those from the sham group
with the dose-response curve shifting to the right
and most significant decrease by 51.42% in the superior mesenteric artery (SMA
P
<
0.05). Propofol treatment significantly improved the hyporeactivity and calcium sensitivity of the vessels isolated from the septic rats
especially those of the femoral artery with a recovery rate of 89.57% (
P
<
0.05). In comparison with the propofol group
the dose-response curves of the propofol+Y-27632 group and the propofol+GO6976 group were shifting to right
indicating that Y-27632 and GO6976 could significantly inhibit the amelioration of propofol on calcium sensitivity of SMA in severely septic rats with an inhibitory rate of 146.95% and 88.63% (
P
<
0.05)
respectively. Isolated vascular reactivity measurement demonstrated that Y-27632 and Movens treatment significantly antagonized the ameliorated role of propofol on hyporeactivity of blood vessels from the septic rats with an inhibitory rate of 40.79% and 169.90% (
P
<
0.05)
separately
while no such effect was observed in the propofol+GO6976 and propofol+2-APB groups.
Conclusion
2
Propofol treatment can significantly improve vascular hyporeactivity of septic rats
which may attribute to the increase of vascular calcium sensitivity through RhoA/ROCK pathway.
关键词
Keywords
references
CHRISTAKI E, OPAL S M. Is the mortality rate for septic shock really decreasing?[J]. Curr Opin Crit Care, 2008, 14(5): 580-586. DOI: 10.1097/mcc.0b013e32830f1e25.
GUARIDO K L, GONÇALVES R P M, JÚNIOR A G, et al . Increased activation of the Rho-A/Rho-kinase pathway in the renal vascular system is responsible for the enhanced reactivity to exogenous vasopressin in endotoxemic rats[J ] . Crit Care Med, 2014, 42(6): e461-e471. DOI: 10.1097/ccm.0000000000000313.
EVANS L, RHODES A, ALHAZZANI W, et al . Surviving sepsis campaign: International Guidelines for Management of Sepsis and Septic Shock 2021[J ] . Intensive Care Med, 2021, 47(11): 1181-1247. DOI: 10.1007/s00134-021-06506-y.
LI T, LIU L M, XU J, et al . Changes of Rho kinase activity after hemorrhagic shock and its role in shock-induced biphasic response of vascular reactivity and calcium sensitivity[J ] . Shock, 2006, 26(5): 504-509. DOI: 10.1097/01.shk.0000228796.41044.41.
YANG G M, LI T, XU J, et al . PKC plays an important mediated effect in arginine vasopressin induced restoration of vascular responsiveness and calcium sensitization following hemorrhagic shock in rats[J ] . Eur J Pharmacol, 2010, 628(1-3): 148-154. DOI: 10.1016/j.ejphar.2009.11.040.
YANG G M, LI T, XU J, et al . Mitogen-activated protein kinases regulate vascular reactivity after hemorrhagic shock through myosin light chain phosphorylation pathway[J ] . J Trauma Acute Care Surg, 2013, 74(4): 1033-1043. DOI: 10.1097/ta.0b013e31828586a2.
DEVLIN J W, ROBERTS R J. Pharmacology of commonly used analgesics and sedatives in the ICU: benzodiazepines, propofol, and opioids[J]. Anesthesiol Clin, 2011, 29(4): 567-585. DOI: 10.1016/j.anclin.2011.09.001.
MARLER J, MOHRIEN K, KIMMONS L A, et al . Effects of propofol on vasopressor use in patients with sepsis and severe sepsis: a pilot study[J ] . J Crit Care, 2016, 35: 155-160. DOI: 10.1016/j.jcrc.2016.05.015.
BOFFA J J, ARENDSHORST W J. Maintenance of renal vascular reactivity contributes to acute renal failure during endotoxemic shock[J]. J Am Soc Nephrol, 2005, 16(1): 117-124. DOI: 10.1681/asn.2004060441.
GERICKE A, MARTINKA P, NAZARENKO I, et al . Impact of α 1 -adrenoceptor expression on contractile properties of vascular smooth muscle cells[J ] . Am J Physiol Regul Integr Comp Physiol, 2007, 293(3): R1215-R1221. DOI: 10.1152/ajpregu.00076.2007..
BAO H G, LI S. Effects of propofol on the outcomes of rats with Sepsis [J ] . J Surg Res, 2011, 168(1): e111-e115. DOI: 10.1016/j.jss.2010.12.034.
TAKEMOTO Y. Dose effects of propofol on hemodynamic and cytokine responses to endotoxemia in rats[J]. J Anesth, 2005, 19(1): 40-44. DOI: 10.1007/s00540-004-0267-z.
DUAN C Y, YANG G M, LI T, et al . Advances in vascular hyporeactivity after shock: the mechanisms and managements[J ] . Shock, 2015, 44(6): 524-534. DOI: 10.1097/shk.0000000000000457.
GONG M C, ⅡZUKA K, NIXON G, et al . Role of guanine nucleotide-binding proteins: ras-family or trimeric proteins or both: in Ca 2+ sensitization of smooth muscle[J ] . Proc Natl Acad Sci USA, 1996, 93(3): 1340-1345. DOI: 10.1073/pnas.93.3.1340..
KAMERITSCH P, POGODA K, RITTER A, et al . Gap junctional communication controls the overall endothelial calcium response to vasoactive agonists[J ] . Cardiovasc Res, 2012, 93(3): 508-515. DOI: 10.1093/cvr/cvr345.
POGODA K, KAMERITSCH P, MANNELL H, et al . Connexins in the control of vasomot or function[J ] . Acta Physiol(Oxf), 2019, 225(1): e13108. DOI: 10.1111/apha.13108.
MING J, LI T, ZHANG Y, et al . Regulatory effects of megj on vascular reactivity following hemorrhagic shock in rats[J ] . Shock, 2008: 1. DOI: 10.1097/shk.0b013e31817d3ef2.
XU J, LI T, YANG G M, et al . Pinacidil pretreatment improves vascular reactivity after shock through PKCα and PKCε in rats[J ] . J Cardiovasc Pharmacol, 2012, 59(6): 514-522. DOI: 10.1097/fjc.0b013e31824d4d75.
YANG G M, PENG X Y, WU Y, et al . Involvement of connexin 43 phosphorylation and gap junctional communication between smooth muscle cells in vasopressin-induced ROCK-dependent vasoconstriction after hemorrhagic shock[J ] . Am J Physiol Cell Physiol, 2017, 313(4): C362-C370. DOI: 10.1152/ajpcell.00258.2016.
XU J, LIU L M. Role of calcium desensitization in vascular hyporeactivity in hemorrhagic shock[J]. Chin Crit Care Med, 2005, 17(1): 20-23. DOI: 10.3760/j.issn:1003-0603.2005.01.008.
LIAO M H, SHIH C C, TSAO C M, et al . RhoA/Rho-kinase and nitric oxide in vascular reactivity in rats with endotoxaem ia[J ] . PLoS One, 2013, 8(2): e56331. DOI: 10.1371/journal.pone.0056331.
WILLIAMS J, BOGWU J, OYEKAN A. The role of the RhoA/Rho-kinase signaling pathway in renal vascular reactivity in endothelial nitric oxide synthase null mice[J]. J Hypertens, 2006, 24(7): 1429-1436. DOI: 10.1097/01.hjh.0000234125.01638.3b.
NGUYEN DINH CAT A, CALLERA G E, FRIEDERICH-PERSSON M, et al . Vascular dysfunction in obese diabetic db/db mice involves the interplay between aldosterone/mineralocorticoid receptor and Rho kinase signaling[J ] . Sci Rep, 2018, 8(1): 2952. DOI: 10.1038/s41598-018-21087-5.