首页> 外文OA文献 >Involvement of substance P present in primary afferent neurones in modulation of cutaneous blood flow in the instep of rat hind paw.
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Involvement of substance P present in primary afferent neurones in modulation of cutaneous blood flow in the instep of rat hind paw.

机译:在大鼠后爪脚背中,初级传入神经元中存在的P物质参与皮肤血流的调节。

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摘要

1. The participation of small-diameter afferent fibres in the microcirculatory haemodynamics of cutaneous tissue was examined by studies on the effects of antidromic stimulation of primary afferent neurones on cutaneous blood flow (CBF) and tachykinin release into the subcutaneous space in the instep of the hind paw of rats. 2. Antidromic stimulation of the sectioned sciatic nerve induced a biphasic flow response, an initial transient decrease followed by an increase, with no alteration in the blood pressure. 3. Neither phase was affected by pretreatment with phentolamine (0.1 mg kg-1, i.a.), propranolol (0.5 mg kg-1, i.a.), atropine (0.5 mg kg-1, i.a.), methysergide (0.5 mg kg-1, i.a.) or mepyramine (10 mg kg-1, i.a.) plus cimetidine (10 mg kg-1, i.a.), but both were significantly inhibited by pretreatment with capsaicin (50 mg kg-1, s.c.). 4. Spantide (1-2 mumol kg-1, i.a.), a substance P (SP) antagonist, reduced the basal CBF, and also inhibited both phases of the biphasic flow response evoked by antidromic stimulation of the sectioned sciatic nerve. 5. Intra-arterial infusion of SP (0.5 mumol kg-1, i.a.) induced a biphasic flow response similar to that elicited by antidromic stimulation of the sectioned sciatic nerve. 6. Antidromic stimulation of the sectioned sciatic nerve caused a marked increase in SP release into the subcutaneous perfusate of the instep of the rat hind paw, but no detectable increase in neurokinin A release.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.通过研究原发传入神经元的反刺激刺激对皮下足背皮下血流(CBF)和速激肽释放的影响,研究了小直径传入纤维在皮肤组织微循环血流动力学中的参与。大鼠的后爪。 2.对坐骨神经的反刺激刺激引起两相血流反应,先是短暂的下降,然后是上升,而血压没有变化。 3.苯妥拉明(0.1 mg kg-1,ia),普萘洛尔(0.5 mg kg-1,ia),阿托品(0.5 mg kg-1,ia),甲基瑟麦角(0.5 mg kg-1, ia)或美吡拉明(10 mg kg-1,ia)加西咪替丁(10 mg kg-1,ia),但两者均被辣椒素(50 mg kg-1,sc)预处理显着抑制。 4. Spantide(1-2 mumol kg-1,i.a.),一种P物质(SP)拮抗剂,降低了基础CBF,还抑制了反切刺激坐骨神经切开引起的两相血流反应的两个阶段。 5.动脉内注入SP(0.5μmol·kg-1,即a.a.)引起双相流响应,类似于反切刺激坐骨神经切开所引起的。 6.对坐骨神经的反刺激刺激导致大鼠后足脚背皮下灌注液中SP的释放显着增加,但神经激肽A的释放没有可检测到的增加(摘要截断为250字)。

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