Hypothesis, we found that isolated ventricular myocytes from hyperthyroid hamsters had

Hypothesis, we found that isolated ventricular myocytes from hyperthyroid hamsters had enhanced mechanical function when compared to age get Triptorelin matched control hamsters, despite the aforementioned adverse chamber remodeling and diminished global cardiac function. Given the close proximity of fibrillar collagen to myocytes and the finding that fibrillar collagen is a relatively stiff material with a tensile strength greater than steel [41], it is likely that even a small increase in collagen can impair cardiomyocyte function. Indeed, this notion is supported by reports that small changes in collagenLV Myocyte/Chamber Function in HyperthyroidismFigure 2. Isolated cardiomyocyte mechanics following 10 months of thyroid hormone treatment. Values are means (SD). A . Cell Length (A); +dL/dT, maximal velocity of shortening (B); L/dT, maximal velocity of re-lengthening (C); Peak Shortening (D); TPS, time to peak shortening (E), TR90, Time to 90 re-lengthening (F). C, control; H, hyperthyroid. N = 527/group. *, p,0.05 vs. control. doi:10.1371/journal.pone.0046655.gFigure 3. LV fibrosis. Values are means (SD). Representative images of LV fibrosis stained by Masson’s Trichrome (A). collagen volume as a proportion of total tissue area (B). C, Control; H, Hyperthyroid. N = 5/group. *, p,0.05 vs. control. doi:10.1371/journal.pone.0046655.gLV Myocyte/Chamber Function in Hyperthyroidismconcentration can have a profound impact on passive mechanical properties of cardiac tissue [31,70]. In agreement, our findings suggest that relatively modest but significant increases in myocardial collagen deposition can impede myocyte contractile ability even when individual myocyte function is enhanced. Consistent with our previous report [19], we did not observe noticeable areas of fibronecrosis. This suggests that the depressed global cardiac function observed during chronic hyperthyroidism is at least in part the product of inhibited myocyte function caused by increased perivascular and interstitial fibrotic deposition and does not appear to be a product of extensive myocyte loss.with our commonly used non-calcium tolerant myocyte preparation with rapid gluteraldehyde fixation (.90 rod cells are routine), the Ca2+ tolerant isolated myocyte preps used here did not produce high enough rod cell yields for accurate Coulter Channelyzer analysis.ConclusionsIn summary, chronic hyperthyroidism was associated with deleterious cardiac remodeling, LV fibrosis, and cardiac functional decline. Despite global cardiac 117793 web impairment, individual isolated cardiac myocytes from chronically hyperthyroid hamsters had normal or enhanced function when compared with myocytes from untreated age matched controls. While we cannot definitely establish a cause and effect relationship, our data strongly suggests that increased LV interstitial fibrosis can undermine the ability of otherwise normal myocytes to function properly. One can only speculate regarding translating ANY animal observations to humans. While chronic hyperthyroidism in humans is generally identified and treated before reaching this point, our results may provide an explanation for LV dysfunction observed in patients with chronic hyperthyroidism.LimitationsOur study has several limitations. While a standard experimental protocol was closely followed to replicate the same experimental conditions for each animal, it is possible that myocytes selected for functional assessment do not represent the total myocyte population within the i.Hypothesis, we found that isolated ventricular myocytes from hyperthyroid hamsters had enhanced mechanical function when compared to age matched control hamsters, despite the aforementioned adverse chamber remodeling and diminished global cardiac function. Given the close proximity of fibrillar collagen to myocytes and the finding that fibrillar collagen is a relatively stiff material with a tensile strength greater than steel [41], it is likely that even a small increase in collagen can impair cardiomyocyte function. Indeed, this notion is supported by reports that small changes in collagenLV Myocyte/Chamber Function in HyperthyroidismFigure 2. Isolated cardiomyocyte mechanics following 10 months of thyroid hormone treatment. Values are means (SD). A . Cell Length (A); +dL/dT, maximal velocity of shortening (B); L/dT, maximal velocity of re-lengthening (C); Peak Shortening (D); TPS, time to peak shortening (E), TR90, Time to 90 re-lengthening (F). C, control; H, hyperthyroid. N = 527/group. *, p,0.05 vs. control. doi:10.1371/journal.pone.0046655.gFigure 3. LV fibrosis. Values are means (SD). Representative images of LV fibrosis stained by Masson’s Trichrome (A). collagen volume as a proportion of total tissue area (B). C, Control; H, Hyperthyroid. N = 5/group. *, p,0.05 vs. control. doi:10.1371/journal.pone.0046655.gLV Myocyte/Chamber Function in Hyperthyroidismconcentration can have a profound impact on passive mechanical properties of cardiac tissue [31,70]. In agreement, our findings suggest that relatively modest but significant increases in myocardial collagen deposition can impede myocyte contractile ability even when individual myocyte function is enhanced. Consistent with our previous report [19], we did not observe noticeable areas of fibronecrosis. This suggests that the depressed global cardiac function observed during chronic hyperthyroidism is at least in part the product of inhibited myocyte function caused by increased perivascular and interstitial fibrotic deposition and does not appear to be a product of extensive myocyte loss.with our commonly used non-calcium tolerant myocyte preparation with rapid gluteraldehyde fixation (.90 rod cells are routine), the Ca2+ tolerant isolated myocyte preps used here did not produce high enough rod cell yields for accurate Coulter Channelyzer analysis.ConclusionsIn summary, chronic hyperthyroidism was associated with deleterious cardiac remodeling, LV fibrosis, and cardiac functional decline. Despite global cardiac impairment, individual isolated cardiac myocytes from chronically hyperthyroid hamsters had normal or enhanced function when compared with myocytes from untreated age matched controls. While we cannot definitely establish a cause and effect relationship, our data strongly suggests that increased LV interstitial fibrosis can undermine the ability of otherwise normal myocytes to function properly. One can only speculate regarding translating ANY animal observations to humans. While chronic hyperthyroidism in humans is generally identified and treated before reaching this point, our results may provide an explanation for LV dysfunction observed in patients with chronic hyperthyroidism.LimitationsOur study has several limitations. While a standard experimental protocol was closely followed to replicate the same experimental conditions for each animal, it is possible that myocytes selected for functional assessment do not represent the total myocyte population within the i.