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1.
Microvasc Res ; 59(1): 88-98, 2000 Jan.
Article in English | MEDLINE | ID: mdl-10625575

ABSTRACT

The quantitative contribution of endothelin and free radicals in modulating peripheral endothelial and smooth muscle-dependent vascular responses in 4 weeks streptozotocin-induced diabetic rats was investigated. Skin blood flow was monitored in base of blisters raised on the hind footpad. Smooth muscle-dependent vasodilation was tested using sodium nitroprusside (SNP). Endothelial-mediated inflammatory responses were induced via either electrical stimulation (ES) of the sciatic nerve or substance P (SP) perfusion over the blister base. Role of endothelin and free radicals was examined using ET-A or ET-B receptor antagonists (BQ-123 or BQ-788) and superoxide anions or hydroxyl radicals scavengers (superoxide dismutase (SOD) or N-acetyl cysteine (NAC)). Diabetic rats showed a significant reduction (75%) in SNP responses that coincided with a 70 and 60% reduction in responses to ES and SP. Their basal plasma extravasation (PE) was significantly higher while PE response to SP was significantly reduced. BQ-788, was more potent than BQ-123, improving responses to ES and SP in diabetic rats by 85%. Likewise, NAC was more potent than SOD normalizing the ES response and improving SP response by 85%. Combined treatment with BQ-123 and SOD normalized all vasodilatation responses in diabetic rats. BQ-123 and BQ-788 were equally potent normalizing the PE responses to SP whereas SOD and NAC had no effect. We conclude that endothelin and free radicals play a role in altering microvascular function in diabetes and that their effect could be reversed early in the disease.


Subject(s)
Diabetes Mellitus, Experimental/physiopathology , Endothelins/physiology , Microcirculation/metabolism , Acetylcysteine/pharmacology , Animals , Antihypertensive Agents/pharmacology , Diabetes Mellitus, Experimental/chemically induced , Electric Stimulation , Endothelin Receptor Antagonists , Free Radicals/metabolism , Laser-Doppler Flowmetry , Male , Microcirculation/drug effects , Nitroprusside/pharmacology , Oligopeptides/pharmacology , Peptides, Cyclic/pharmacology , Piperidines/pharmacology , Rats , Rats, Sprague-Dawley , Receptor, Endothelin A , Receptor, Endothelin B , Sciatic Nerve , Skin/blood supply , Skin/drug effects , Streptozocin , Substance P/pharmacology , Superoxide Dismutase/pharmacology , Vasodilator Agents/pharmacology
2.
Chin Med J (Engl) ; 112(11): 1028-31, 1999 Nov.
Article in English | MEDLINE | ID: mdl-11721466

ABSTRACT

OBJECTIVE: To study the effect of diabetes on the creatine kinase (CK) activity in different tissues of streptozotocin-induced diabetic rats. METHODS: Serum samples, heart, extensor digitorum longus, brain and bladder were collected from both streptozotocin-induced diabetic rat and control group. Ck was measured by enzymologic method. RESULTS: The body weight, heart weight and brain weight were reduced significantly compared with control group (P < 0.001), but bladder weight was increased significantly (P < 0.001). CK activity in serum and extensor digitorum longus in diabetic rat was significantly lower (P < 0.001); CK activity in diabetic heart was lower (P < 0.01); and in brain also lower (P < 0.05). A higher CK activity in diabetic bladder was found (P < 0.001). CONCLUSIONS: Diabetes can result in a lower CK activity in serum, heart, brain and extensor digitorum longus that may affect the energy metabolism in the tissues. A higher CK activity in diabetic bladder may reflect a functional compensatory mechanism.


Subject(s)
Creatine Kinase/metabolism , Diabetes Mellitus, Experimental/enzymology , Animals , Brain/enzymology , Male , Myocardium/enzymology , Rats , Rats, Sprague-Dawley , Urinary Bladder/enzymology
3.
Inflamm Res ; 45(8): 380-5, 1996 Aug.
Article in English | MEDLINE | ID: mdl-8872510

ABSTRACT

A supersensitivity to the neuropeptide substance P (SP) has been shown to develop in post-terminal membranes of many denervated tissues. This study examined changes in the sensitivity of post-terminal vascular receptors to SP and calcitonin gene-related peptide (CGRP) in rat skin microvasculature following sciatic nerve section. In anaesthetised rats, 0.5 cm of sciatic nerve in the right mid-thigh region was removed. Two weeks later, SP (100 microM) and sodium nitroprusside (SNP, 1 mM), a direct smooth muscle vasodilator, were introduced into denervated intact footpad skin, via the electrophoresis technique. Laser doppler flowmeter was used to record changes in relative blood flow in the rat hind footpad. The results showed a significant increase in SP response over controls and slight increase in smooth muscle reactivity as determined by an increase in the vascular response to SNP. In another set of experiments, the sensitivity of post-terminal receptors was examined over a 4 weeks period in an acutely injured footpad skin of sciatic nerve lesioned rats. A vacuum-induced blister was raised on the hind footpad and SP, CGRP (each at 1 microM) or SNP (100 microM) were superfused over the blister base. In nerve lesioned rats, using the acutely injured footpad skin model, the results showed a reduction in the vascular responses to SP, CGRP and SNP. The response to SP continued to decrease over time reaching 22% of control values by 4 weeks. Responses to SNP and CGRP were reduced to 53% and 45% respectively by 2 weeks and then improved to 75% of control values by 4 weeks. Possible contributions of sympathetic efferents and the saphenous nerve to these reduced responses in acutely injured skin of nerve lesioned rats were examined using guanethidine (50 mg/kg i.p.) or sectioned saphenous nerve respectively. These procedures did not significantly modify the reduced vascular responses in the blister base of lesioned rats. Possible activation of endogenous opioids and/or the release of endothelin due to blister induction in nerve lesioned rats was examined using naloxone and the endothelin receptor antagonist, BQ-123, respectively. Treatment with naloxone increased SP response in lesioned rats to 41% of control value with no change in smooth muscle reactivity. BQ-123 significantly increased the responses to SP and SNP to 51% and 100% of their own control values respectively. It is concluded that supersensitivity of post-terminal vascular receptors develops in intact skin following chronic nerve lesion. On the other hand, acute injury of the denervated skin area induces activation of endogenous inhibitory modulatory mechanisms that masks this supersensitivity.


Subject(s)
Dermatitis/pathology , Sciatic Nerve/injuries , Skin/innervation , Anesthesia , Animals , Blister/pathology , Calcitonin Gene-Related Peptide/pharmacology , Denervation , Dermatitis/etiology , Electrophoresis , Endothelin Receptor Antagonists , Male , Naloxone/pharmacology , Narcotic Antagonists/pharmacology , Nitroprusside/administration & dosage , Nitroprusside/pharmacology , Peptides, Cyclic/pharmacology , Rats , Rats, Sprague-Dawley , Regional Blood Flow/physiology , Sciatic Nerve/physiopathology , Skin/blood supply , Skin/pathology , Substance P/administration & dosage , Substance P/pharmacology , Vasodilator Agents/administration & dosage , Vasodilator Agents/pharmacology
4.
Brain Res ; 651(1-2): 227-35, 1994 Jul 18.
Article in English | MEDLINE | ID: mdl-7522933

ABSTRACT

The primary constituent of the senile plaque core in Alzheimer's disease (AD) is the beta-amyloid protein (beta A4). A discrete 11 amino acid fragment of the beta A4, beta A4(25-35), has been implicated in mediating in vitro neurotoxicity and an inflammatory response surrounding senile plaques in AD via interaction with the Serpin Enzyme Complex (SEC) receptor. Substance P (SP), a neuropeptide of the tachykinin family and a major mediator of neurogenic inflammation, shows sequence homology to beta A4(25-35) and has been shown to protect against the neurotoxicity of beta-amyloid. SP also competes with beta A4(25-35) for binding to the SEC-receptor. SP neurons have also been found to be depleted in AD. Using a blister model of inflammation in the rat hind footpad, we have examined the effect of beta A4(25-35) and its interaction with SP in rat skin microvasculature and determined age-related changes to these phenomena. In addition, pharmacological manipulation of these responses using SEC-receptor ligands (peptide 105Y and 105C) was also undertaken. Because of the evidence for co-existence and co-release of SP and calcitonin gene-related peptide (CGRP) from the peripheral terminals of sensory nerves, it was of interest to examine the interaction of CGRP with beta A4(25-35) on rat skin microvasculature. beta A4(25-35) (10 microM) was perfused over the base of a blister raised on the hind footpad of anaesthetised young and old rats. This was followed by perfusion of SP (1 microM) or CGRP (1 microM) after Ringer's solution. Relative blood flow was monitored using a Laser-Doppler Flowmeter.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Amyloid beta-Peptides/metabolism , Peptide Fragments/metabolism , Receptors, Cell Surface/metabolism , Substance P/metabolism , Amyloid beta-Peptides/pharmacology , Animals , Calcitonin Gene-Related Peptide/metabolism , Calcitonin Gene-Related Peptide/pharmacology , Ligands , Male , Microcirculation , Peptide Fragments/pharmacology , Rats , Rats, Sprague-Dawley , Skin/blood supply , Substance P/pharmacology , Vasoconstriction/drug effects , Vasodilation/drug effects
5.
Brain Res ; 641(2): 265-72, 1994 Apr 04.
Article in English | MEDLINE | ID: mdl-7516812

ABSTRACT

Human studies have shown an age-related decrease in modulation of skin vascular reactivity by sensory nerves that correlates with a decline in wound repair efficacy. Using a vacuum-induced blister model in the rat hind footpad, we have investigated age-related changes in pre- and post-terminal activity of primary afferents involved in skin neurovascular function. Changes in local skin blood flow were monitored using a laser Doppler flowmeter. Pre-terminal stimulation was achieved by electrical stimulation of the distal end of the sciatic nerve (10 V, 15 Hz and 0.5 ms) in three groups of young, old and neonatally pretreated capsaicin rats (3, 24 and 3 months old, respectively). The effect of post-terminal stimulation, achieved using local perfusion of 1 microM substance P (SP) over the blister base, was examined in young (3 months old), mature (12 months old) and aged (24 months old) rats. In addition to changes in SP responsiveness, other post-terminal changes studied included changes in smooth muscle reactivity to sodium nitroprusside (SNP), which acts directly on smooth muscle and to endothelial cell function using N-nitro-L-arginine (L-NORAG), a selective inhibitor of nitric oxide synthesis and endothelium-dependent relaxation. Electrical stimulation of the sciatic nerve in young rats induced an increase in local blood flow (within 1 min) that was maintained during the stimulation period, while the capsaicin group and the old group showed a significantly increased latency and decreased amplitude of the response.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Neurons, Afferent/physiology , Sciatic Nerve/physiology , Skin Aging/physiology , Skin/innervation , Afferent Pathways/growth & development , Afferent Pathways/physiology , Animals , Arginine/analogs & derivatives , Arginine/pharmacology , Blister/physiopathology , Capsaicin/pharmacology , Electric Stimulation , Female , Humans , Male , Neurons, Afferent/drug effects , Nitroarginine , Nitroprusside/pharmacology , Rats , Rats, Sprague-Dawley , Regional Blood Flow , Skin/blood supply , Skin/drug effects , Substance P/pharmacology , Vasodilation
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