Modulation by pH o and Intracellular Ca 2+ of Na + -H + Exchange in Diabetic Rat Isolated Ventricular Myocytes

Autor: D. Feuvray, Dominique Lagadic-Gossmann, Karine Le Prigent
Rok vydání: 1997
Předmět:
Zdroj: Circulation Research. 80:253-260
ISSN: 1524-4571
0009-7330
DOI: 10.1161/01.res.80.2.253
Popis: We have previously shown that diabetes is associated with a decrease in Na + -H + exchange activity in rat cardiac papillary muscle. The present work has been carried out in order to elucidate the factors responsible for such an alteration. Thus, we have studied the effects of pH o and intracellular Ca 2+ on Na + -H + exchange in ventricular myocytes isolated from streptozotocin-induced diabetic rat hearts. pH i was recorded using carboxy-seminaphthorhodafluor (SNARF-1). The NH 4 + (10 mmol/L) prepulse method was used to induce an acid load in order to activate Na + -H + exchange in HEPES-buffered Tyrode's solution. Whereas diabetes did not change intracellular buffering power, it significantly decreased acid efflux through Na + -H + exchange (acid efflux, 4.32±0.4 [n=32, normal cells] versus 2.5±0.2 [n=43, diabetic cells] meq/L per minute at pH i 6.9; P o (at a range of 8.0 to 6.8), acid efflux similarly varied in normal and diabetic cells, thus pointing to an unchanged pH o sensitivity of Na + -H + exchange. Buffering of intracellular Ca 2+ by pretreatment of the cells with BAPTA-AM (25 μmol/L, Ca 2+ -chelator) resulted in a decrease by ≈58% of acid efflux in the diabetic group. This decrease was even more marked in normal cells (by ≈74%). Interestingly, the pH i dependence of the acid efflux carried by Na + -H + exchange then became identical in both groups of cells, thus pointing to a role for intracellular Ca 2+ in the diabetes-related alterations of the exchange. Inhibition of calmodulin (by 1.5 μmol/L calmidazolium) and of Ca 2+ /calmodulin-dependent protein kinase II (by 2 μmol/L 1-[ N , O -bis(5-isoquinolinesulfonyl)- N -methyl- l -tyrosyl]-4-phenylpiperazine [KN-62]) significantly slowed down pH i recovery in both normal and diabetic cells. However, the effect of KN-62 was significantly lower in diabetic cells (efflux decreased by ≈17%) compared with normal cells (decrease by 45%). In conclusion, these data, in light of recent observations showing a decreased [Ca 2+ ] i associated with diabetes in isolated ventricular myocytes, suggest that changes in intracellular Ca 2+ may play an important role in altering Na + -H + exchange activity in diabetic ventricular myocytes. They also point to diabetes-related alterations in the Ca 2+ /calmodulin protein kinase II–dependent phosphorylation of Na + -H + exchange.
Databáze: OpenAIRE
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