Vascular relaxation response to hydrogen peroxide is impaired in hypertension
Bibliographic record
Abstract
1. In phenylephrine (1 microm)-precontracted rat superior mesenteric arteries (MA), hydrogen peroxide (H(2)O(2), 0.3 and 1 mm) caused a biphasic response: a transient contraction followed by a relaxation. In the presence of thromboxane A(2)/prostaglandin H(2) (TP) receptor antagonist (SQ 29548), the contractile component of the biphasic response was abolished. The relaxation response to H(2)O(2) was smaller in spontaneously hypertensive rats (SHR) when compared with normotensive Wistar-Kyoto rats (WKY). 2. The mechanisms for the attenuated relaxation to H(2)O(2) in the SHR were studied. KCl (40 mm) prevented the relaxation response. Calcium-dependent K(+) channel (K(Ca)) blockers (tetraethylammonium chloride, TEA; iberiotoxin, and charybdotoxin) showed a greater inhibition of H(2)O(2) relaxation in SHR than in WKY, whereas voltage-dependent K(+)-channel (K(v)) blocker 4-aminopyridine was more effective in inhibiting the relaxation in WKY than in SHR. 3. H(2)O(2) (1 mm) greatly enhanced the frequency and intensity of the spontaneous transient outward K(+) currents in SHR MA, and the effects of H(2)O(2) were inhibited by iberiotoxin, while in WKY MA the K(+) currents induced by H(2)O(2) were mainly of the K(v) type. The consequence of the activation of different types of K(+) channel was that the net increase in mean outward K(+) current density in response to H(2)O(2) was smaller in SHR than in WKY, which may account for the attenuated relaxation response to H(2)O(2) in the SHR. 4. The contractile responses of MA to TEA, iberiotoxin, and charybdotoxin were greater in SHR than in WKY. 5. In summary, an attenuated relaxation response to H(2)O(2) was found in SHR MA when compared to WKY. In contrast to the activation of K(v) channels in WKY, H(2)O(2) markedly enhanced K(Ca) activity in SHR, resulting in an attenuation of the increase in mean outward K(+) current density in response to H(2)O(2). These results suggest that alteration in K(+) channel activation by reactive oxygen species may play a role in the development of hypertension in SHR.
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How this classification was reachedexpand
Full frame machine prediction
Teacher imitationNot calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.
Distilled classifier scores by category (both heads)
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.000 | 0.000 |
| Meta-epidemiology (narrow) | 0.000 | 0.000 |
| Meta-epidemiology (broad) | 0.001 | 0.000 |
| Bibliometrics | 0.000 | 0.000 |
| Science and technology studies | 0.000 | 0.000 |
| Scholarly communication | 0.000 | 0.000 |
| Open science | 0.000 | 0.000 |
| Research integrity | 0.000 | 0.001 |
| Insufficient payload (model declined to judge) | 0.001 | 0.000 |
Machine scores (provisional)
The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.
Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from itClassification
machine, unvalidatedMachine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.
How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".